polypeptide constructs that selectively bind to CLDN6 and CD3

Abstract

The present invention relates to a polypeptide or polypeptide construct comprising a domain that binds to claudin 6 (CLDN6) and another domain that binds to CD3. The present invention also provides a polynucleotide encoding the construct, a vector containing the polynucleotide, and a host cell transformed or transfected with the polynucleotide or vector. The present invention also provides a method for producing the construct of the present invention, medical uses of the construct, and a kit containing the construct.

Description

[Technical Field]

[0001] The present invention relates to a polypeptide / polypeptide construct comprising a domain containing a paratope that binds to claudin 6 (CLDN6) and another domain containing a paratope that binds to CD3. Furthermore, the present disclosure provides a polynucleotide encoding the polypeptide / polypeptide construct, a vector containing the polynucleotide, and host cells transformed or transfected with the polynucleotide or vector. Furthermore, the present invention provides a process for producing the polypeptide / polypeptide construct of the present invention, the medical use of the polypeptide / polypeptide construct, and a kit containing the construct. [Background technology]

[0002] Claudins are essential structural and functional components of epithelial tight junctions located between two adjacent cells, regulating cell-cell permeability, maintaining ionic homeostasis, and supporting cell adhesion and polarity. Claudins are 22-27 kDa four-transmembrane proteins that form protective walls by multimerizing within or across the cell membrane. The 24 reported claudin proteins differ in their tissue localization and expression, as well as their interactions with other proteins.

[0003] Claudin 6 (CLDN6) was first identified through a similarity search of further genes and proteins belonging to the claudin family of genes and proteins (Morita et al., Proc. Natl. Acad. Sci. USA, Vol. 96, pp. 511-516, 1999). Claudin 6 mRNA expression was not detected in adult tissues, but only in embryonic tissues. Subsequently, mRNA and protein expression were detected in various tumors and tumor cell lines. Consistent with these findings, claudin 6 is considered a carcinoembryonic transmembrane protein that is not present in normal adult human tissues. CLDN6 expression is abnormally activated in various cancer types, including ovarian cancer, lung cancer, gastric cancer, breast cancer, germline cancer, and childhood cancers ((Stadler et al., Onocoimmunology 2016, Vol.5, No.3, e1091555 and the references cited therein, e.g., Micke et al, Int.J.Cancer 2014:2206-14; Rendon-Huerta et al., J.Gastrointest.Cancer 2010;41:52-59; Ushiku et al., Histopathology 2012,61:1043-56); Ben-David et al., Nat.Commun.2013;4:1992; Birks et al., BRAIN PATHOL.2010;20:140-50), Sullivan et al., Am. J. Surg. Pathol. 2012;36:73-80).

[0004] CLDN6 is a 220-amino acid protein with two extracellular loops (ECLs), and it has substantial sequence identity with CLDN9, which has only three different amino acid residues in its two ECLs.

[0005] CLDN6 expression in multiple tumor types is restricted in normal tissue expression during fetal development, leading to its consideration as a therapeutic target in various types of cancer, such as ovarian and non-small cell lung cancer (NSCLC), and other indications.

[0006] Ovarian cancer and NSCLC cancer remain indications with a high level of unmet medical need.

[0007] Ovarian cancer is the seventh most common cancer worldwide. In 2018, there were 295,414 new cases and 184,799 deaths worldwide, with mortality rates higher in Northern Hemisphere countries than in Asia or Africa (Bray et al., CA Cancer J Clin 2018). Typical first-line treatments include surgery and combination chemotherapy, including platinum and paclitaxel or docetaxel. More recently, the anti-VEGF antibody bevacizumab and PARP inhibitors have been approved as maintenance therapy after first-line chemotherapy. However, despite the initial response, up to 70% of patients experience disease recurrence due to the development of chemotherapy resistance and / or tumor immune evasion. Ovarian tumors are characterized by a highly immunosuppressive tumor microenvironment, and while there is evidence that ovarian tumors can be immunogenic, immune checkpoint therapies, which have modified standard treatments in other solid tumor types, have shown limited durability in ovarian cancer (Rodriguez et al., Cancers 2018). Despite advances in multiple novel therapies and combinations in clinical trials for ovarian cancer, the five-year survival rate remains low, and there is an urgent need for treatments that can enable a lasting response.

[0008] Lung cancer is one of the most common cancers worldwide, with over 2 million new cases and 1.7 million deaths reported in 2018 (Bray et al., CA: A Cancer Journal for Clinicians 2018). Non-small cell lung cancer (NSCLC) accounts for the majority (85%) of lung cancer cases and is often associated with smoking and environmental exposure such as asbestos (Zappa and Mousa, Transl Lung Cancer Res 2016). The recommended first-line treatment for NSCLC is immune checkpoint blockade with platinum doublet chemotherapy for patients whose tumors express PD-L1, although targeted therapy may be preferable for initial treatment of tumors with driver mutations (Ettinger et al., JNCCN, 2019). These advances are promising and have enabled long-lasting responses for some patients with immune checkpoint blockade (Santini and Hellman, Cancer J 2018), but further evaluation of combination immunotherapy and further advances in new therapies are needed to treat most patients.

[0009] Therefore, there is still a need for new therapies that could provide a lasting response to a larger patient population, for the treatment of ovarian cancer and / or NSCLC, particularly for the treatment of any type of cancer that expresses CLDN6, and more specifically for the treatment of cancer patients receiving second-line or higher treatment, such as patients who have previously received chemotherapy or immunotherapy and have recurrent disease.

[0010] A bispecific (and multiplespecific) construct containing one antigen-binding (more precisely, epitope-binding) domain that binds to CD3 on T cells and another antigen-binding (more precisely, epitope-binding) domain that binds to a protein expressed on target cells directly ligates T cells to target cells, inducing T cell retargeting lysis. This mechanism of action differs from chemotherapy, targeted therapies, and other immunotherapies in that it can function on any CD3-positive T cell independently of costimulatory activation signals (Klinger et al., Immunol Reviews 2016).

[0011] The expression of CLDN6 on the cell surface of germ cell tumors, ovarian cancer, and non-small cell lung cancer provides a basis for targeting these tumor types with CLDN6xCD3 polypeptide / polypeptide constructs. Furthermore, CLDN6xCD3 polypeptide / polypeptide constructs have the potential to target further tumor types expressing CLDN6, particularly any type of cancer expressing CLDN6, more specifically, cancer patients receiving second-line or higher treatment, such as those with a history of chemotherapy or immunotherapy and recurrent disease. [Prior art documents] [Non-patent literature]

[0012] [Non-Patent Document 1] Morita et al.,Proc.Natl.Acad.Sci.USA,Vol.96,pp.511-516,1999 [Non-Patent Document 2] Stadler et al.,Onocoimmunology 2016,Vol.5,No.3,e1091555 [Non-Patent Document 3] Micke et al,Int.J.Cancer 2014:2206-14 [Non-Patent Document 4] Rendon-Huerta et al.,J.Gastrointest.Cancer 2010;41:52-59 [Non-Patent Document 5] Ushiku et al., Histopathology 2012,61:1043-56 [Non-Patent Document 6] Ben-David et al.,Nat.Commun.2013;4:1992 [Non-Patent Document 7] Birks et al.,BRAIN PATHOL.2010;20:140-50 [Non-Patent Document 8] Sullivan et al., Am. J. Surg. Pathol. 2012;36:73-80

Non-Patent Document 9

Non-Patent Document 10

[0015] Furthermore, the present invention provides a polypeptide / polypeptide construct comprising or consisting of a domain that includes a paratope (i.e., an antigen-binding domain, more specifically an epitope-binding structure) that binds to CLDN6, and optionally, the domain of the polypeptide / polypeptide construct of the present invention that includes the paratope (i.e., the antigen-binding (epitope-binding) structure) can bind to CLDN6 on the surface of cells expressing CLDN6 and bind to the E1A and / or E2B regions (SEQ ID NO: 1) of CLDN6. Accordingly, the present invention provides a polypeptide / polypeptide construct comprising or consisting of a domain that binds to CLDN6, and optionally, the domain can bind to CLDN6 on the surface of cells expressing CLDN6 that binds to the E1A and / or E2B regions of the sequences corresponding to these loops shown in SEQ ID NOs: 9 and 10.

[0016] In embodiments of the present invention, a polypeptide / polypeptide construct comprising or comprising a domain containing a paratope (i.e., an antigen-binding domain, more specifically, an epitope-binding structure) that binds to CLDN6, and optionally binds to CLDN6 on the surface of a cell expressing CLDN6, and binds to the E1A and / or E2B regions of CLDN6 (SEQ ID NO: 1), wherein the domain containing the paratope (i.e., an antigen-binding (epitope-binding) structure) of the polypeptide / polypeptide construct of the present invention does not bind to amino acids 138-150 of CLDN6 as shown in SEQ ID NO: 1. In further embodiments of the present invention, a polypeptide / polypeptide construct comprising or comprising a domain that binds to CLDN6 binds to the E1A and / or E2B regions of CLDN6 (SEQ ID NO: 1), and does not bind to amino acids 138-150 of CLDN6 as shown in SEQ ID NO: 1.

[0017] Accordingly, the present invention provides a polypeptide / construct comprising a domain comprising a paratope (i.e., an antigen-binding domain, more specifically an epitope-binding structure) that binds to an epitope region comprising amino acids of the extracellular loop 1 (ECL1) of CLDN6 on the surface of a target cell, preferably amino acids 29-39 of SEQ ID NO: 1, and / or amino acids of the extracellular loop 2 (ECL2) of CLDN6 corresponding to amino acids 151-160 of SEQ ID NO: 1. Accordingly, the present invention provides a polypeptide / construct comprising a domain comprising a domain comprising a paratope (i.e., an antigen-binding domain, more specifically an epitope-binding structure) that binds to an epitope region comprising amino acids of the extracellular loop 1 (ECL1) of CLDN6 on the surface of a target cell, preferably amino acids 29-39 of SEQ ID NO: 1, and / or amino acids of the extracellular loop 2 (ECL2) of CLDN6 corresponding to amino acids 151-160 of SEQ ID NO: 1.

[0018] Accordingly, the present invention provides a polypeptide / polypeptide construct as defined in any one of the preceding paragraphs, comprising another domain containing a paratope (i.e., an antigen-binding structure (epitope-binding structure)) that recognizes and / or binds to an extracellular epitope of a CD3ε chain (preferably human and macaque CD3ε chains), and a domain (HLE domain) that extends the half-life of the polypeptide after administration to an individual, optionally comprising two polypeptide monomers comprising a hinge, a CH2 domain, and a CH3 domain, respectively. Accordingly, the present invention provides a polypeptide / polypeptide construct as defined in any one of the preceding paragraphs, comprising another domain containing a paratope (i.e., an antigen-binding structure (epitope-binding structure)) that recognizes and / or binds to an extracellular epitope of a CD3ε chain (preferably human and macaque CD3ε chains), and a domain (HLE domain) that extends the half-life of the polypeptide after administration to an individual, optionally comprising two polypeptide monomers comprising a hinge, a CH2 domain, and a CH3 domain, respectively.

[0019] According to the present invention, polypeptides / polypeptide constructs are provided, the domain of the construct immunoselectively binds to an epitope of CLDN6 that is recognized and / or bound by a paratope (antigen-binding or epitope-binding structure) contained in any one of the sequences referred to in a) to s) below, a) to d), n) and s) are preferred, and a) to c), e) and s) are much preferred. a) The VH region including CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and the VL region including CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO: 18; b) The VH region including CDR-H1 shown in SEQ ID NO: 27, CDR-H2 shown in SEQ ID NO: 28, and CDR-H3 shown in SEQ ID NO: 29, and the VL region including CDR-L1 shown in SEQ ID NO: 30, CDR-L2 shown in SEQ ID NO: 31, and CDR-L3 shown in SEQ ID NO: 32; c) The VH region including CDR-H1 shown in SEQ ID NO: 41, CDR-H2 shown in SEQ ID NO: 42, and CDR-H3 shown in SEQ ID NO: 43, and the VL region including CDR-L1 shown in SEQ ID NO: 44, CDR-L2 shown in SEQ ID NO: 45, and CDR-L3 shown in SEQ ID NO: 46; d) The VH region including CDR-H1 shown in SEQ ID NO: 55, CDR-H2 shown in SEQ ID NO: 56, and CDR-H3 shown in SEQ ID NO: 57, and the VL region including CDR-L1 shown in SEQ ID NO: 58, CDR-L2 shown in SEQ ID NO: 59, and CDR-L3 shown in SEQ ID NO: 60; e) The VH region including CDR-H1 shown in SEQ ID NO: 69, CDR-H2 shown in SEQ ID NO: 70, and CDR-H3 shown in SEQ ID NO: 71, and the VL region including CDR-L1 shown in SEQ ID NO: 72, CDR-L2 shown in SEQ ID NO: 73, and CDR-L3 shown in SEQ ID NO: 74; f) The VH region including CDR-H1 shown in SEQ ID NO: 83, CDR-H2 shown in SEQ ID NO: 84, and CDR-H3 shown in SEQ ID NO: 85, and the VL region including CDR-L1 shown in SEQ ID NO: 86, CDR-L2 shown in SEQ ID NO: 87, and CDR-L3 shown in SEQ ID NO: 88; g) The VH region including CDR-H1 shown in SEQ ID NO: 97, CDR-H2 shown in SEQ ID NO: 98, and CDR-H3 shown in SEQ ID NO: 99, and the VL region including CDR-L1 shown in SEQ ID NO: 100, CDR-L2 shown in SEQ ID NO: 101, and CDR-L3 shown in SEQ ID NO: 102; h) A VH region including CDR-H1 shown in SEQ ID NO: 111, CDR-H2 shown in SEQ ID NO: 112, and CDR-H3 shown in SEQ ID NO: 113, and a VL region including CDR-L1 shown in SEQ ID NO: 114, CDR-L2 shown in SEQ ID NO: 115, and CDR-L3 shown in SEQ ID NO: 116; i) The VH region including CDR-H1 shown in SEQ ID NO: 125, CDR-H2 shown in SEQ ID NO: 126, and CDR-H3 shown in SEQ ID NO: 127, and the VL region including CDR-L1 shown in SEQ ID NO: 128, CDR-L2 shown in SEQ ID NO: 129, and CDR-L3 shown in SEQ ID NO: 130; j) The VH region including CDR-H1 shown in SEQ ID NO: 139, CDR-H2 shown in SEQ ID NO: 140, and CDR-H3 shown in SEQ ID NO: 141, and the VL region including CDR-L1 shown in SEQ ID NO: 142, CDR-L2 shown in SEQ ID NO: 143, and CDR-L3 shown in SEQ ID NO: 144; k) The VH region including CDR-H1 shown in SEQ ID NO: 153, CDR-H2 shown in SEQ ID NO: 154, and CDR-H3 shown in SEQ ID NO: 155, and the VL region including CDR-L1 shown in SEQ ID NO: 156, CDR-L2 shown in SEQ ID NO: 157, and CDR-L3 shown in SEQ ID NO: 158; l) The VH region including CDR-H1 shown in SEQ ID NO: 167, CDR-H2 shown in SEQ ID NO: 168, and CDR-H3 shown in SEQ ID NO: 169, and the VL region including CDR-L1 shown in SEQ ID NO: 170, CDR-L2 shown in SEQ ID NO: 171, and CDR-L3 shown in SEQ ID NO: 172; m) The VH region including CDR-H1 shown in SEQ ID NO: 181, CDR-H2 shown in SEQ ID NO: 182, and CDR-H3 shown in SEQ ID NO: 183, and the VL region including CDR-L1 shown in SEQ ID NO: 184, CDR-L2 shown in SEQ ID NO: 185, and CDR-L3 shown in SEQ ID NO: 186; n) The VH region including CDR-H1 shown in SEQ ID NO: 195, CDR-H2 shown in SEQ ID NO: 196, and CDR-H3 shown in SEQ ID NO: 197, and the VL region including CDR-L1 shown in SEQ ID NO: 198, CDR-L2 shown in SEQ ID NO: 199, and CDR-L3 shown in SEQ ID NO: 200; o) The VH region including CDR-H1 shown in SEQ ID NO: 209, CDR-H2 shown in SEQ ID NO: 210, and CDR-H3 shown in SEQ ID NO: 211, and the VL region including CDR-L1 shown in SEQ ID NO: 212, CDR-L2 shown in SEQ ID NO: 213, and CDR-L3 shown in SEQ ID NO: 214; p) The VH region including CDR-H1 shown in SEQ ID NO: 223, CDR-H2 shown in SEQ ID NO: 224, and CDR-H3 shown in SEQ ID NO: 225, and the VL region including CDR-L1 shown in SEQ ID NO: 226, CDR-L2 shown in SEQ ID NO: 227, and CDR-L3 shown in SEQ ID NO: 228; q) The VH region including CDR-H1 shown in SEQ ID NO: 237, CDR-H2 shown in SEQ ID NO: 238, and CDR-H3 shown in SEQ ID NO: 239, and the VL region including CDR-L1 shown in SEQ ID NO: 240, CDR-L2 shown in SEQ ID NO: 241, and CDR-L3 shown in SEQ ID NO: 242; r) The VH region including CDR-H1 shown in SEQ ID NO: 251, CDR-H2 shown in SEQ ID NO: 252, and CDR-H3 shown in SEQ ID NO: 253, and the VL region including CDR-L1 shown in SEQ ID NO: 254, CDR-L2 shown in SEQ ID NO: 255, and CDR-L3 shown in SEQ ID NO: 256; s) The VH region including CDR-H1 shown in SEQ ID NO: 265, CDR-H2 shown in SEQ ID NO: 266, and CDR-H3 shown in SEQ ID NO: 267, and the VL region including CDR-L1 shown in SEQ ID NO: 268, CDR-L2 shown in SEQ ID NO: 269, and CDR-L3 shown in SEQ ID NO: 270; and t) A VH region comprising CDR-H1 shown in SEQ ID NO: 680, CDR-H2 shown in any one of SEQ ID NOs. 681, 682, or 683, and CDR-H3 shown in any one of SEQ ID NOs. 684, 685, 686, or 687; a VL region comprising CDR-L1 shown in any one of SEQ ID NOs. 688 or 689, CDR-L2 shown in SEQ ID NO: 690, and CDR-L3 shown in any one of SEQ ID NOs. 691, 692, 693, or 694; and any possible combination of heavy and light chains with the CDRs described herein.

[0020] Therefore, the construct of the preceding paragraph preferably includes at least one domain containing a paratope bound to CLDN6 as defined in sections (a) to (s), and optionally further includes a domain containing a domain for CD3. For example, the construct of the preceding paragraph therefore preferably has a VL region and / or a VH region bound to CLDN6 and containing a CDR as defined in sections (a) to (s), and optionally further includes a domain containing a domain for CD3.

[0021] The present invention provides a polypeptide / polypeptide construct comprising a domain comprising a VH region comprising CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and a VL region comprising CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO: 18, which (immunoselectively) binds to an epitope recognized by that domain.

[0022] The present invention provides a polypeptide / polypeptide construct comprising a domain comprising a VH region comprising CDR-H1 shown in SEQ ID NO: 27, CDR-H2 shown in SEQ ID NO: 28, and CDR-H3 shown in SEQ ID NO: 29, and a VL region comprising CDR-L1 shown in SEQ ID NO: 30, CDR-L2 shown in SEQ ID NO: 31, and CDR-L3 shown in SEQ ID NO: 32, which binds (immunoselectively) to an epitope recognized by a domain comprising the above. In other words, the present invention provides a polypeptide / polypeptide construct comprising a domain comprising a VH region comprising CDR-H1 shown in SEQ ID NO: 27, CDR-H2 shown in SEQ ID NO: 28, and CDR-H3 shown in SEQ ID NO: 29, and a VL region comprising CDR-L1 shown in SEQ ID NO: 30, CDR-L2 shown in SEQ ID NO: 31, and CDR-L3 shown in SEQ ID NO: 32, which binds (immunoselectively) to an epitope recognized by a domain comprising the above.

[0023] The present invention provides a polypeptide / polypeptide construct comprising a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 41, CDR-H2 shown in SEQ ID NO: 42, and CDR-H3 shown in SEQ ID NO: 43, and a VL region including CDR-L1 shown in SEQ ID NO: 44, CDR-L2 shown in SEQ ID NO: 45, and CDR-L3 shown in SEQ ID NO: 46, which binds (immunoselectively) to an epitope recognized by that domain. Accordingly, the present invention provides a polypeptide / polypeptide construct comprising a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 41, CDR-H2 shown in SEQ ID NO: 42, and CDR-H3 shown in SEQ ID NO: 43, and a VL region including CDR-L1 shown in SEQ ID NO: 44, CDR-L2 shown in SEQ ID NO: 45, and CDR-L3 shown in SEQ ID NO: 46, which binds (immunoselectively) to an epitope recognized by that domain.

[0024] The present invention provides a polypeptide / polypeptide construct comprising a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 69, CDR-H2 shown in SEQ ID NO: 70, and CDR-H3 shown in SEQ ID NO: 71, and a VL region including CDR-L1 shown in SEQ ID NO: 72, CDR-L2 shown in SEQ ID NO: 73, and CDR-L3 shown in SEQ ID NO: 74, which binds (immunoselectively) to an epitope recognized by that domain. Accordingly, the present invention provides a polypeptide / polypeptide construct comprising a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 69, CDR-H2 shown in SEQ ID NO: 70, and CDR-H3 shown in SEQ ID NO: 71, and a VL region including CDR-L1 shown in SEQ ID NO: 72, CDR-L2 shown in SEQ ID NO: 73, and CDR-L3 shown in SEQ ID NO: 74, which binds (immunoselectively) to an epitope recognized by that domain.

[0025] The present invention provides a polypeptide / polypeptide construct comprising a domain containing a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope recognized by a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 195, CDR-H2 shown in SEQ ID NO: 196, and CDR-H3 shown in SEQ ID NO: 197, and a VL region including CDR-L1 shown in SEQ ID NO: 198, CDR-L2 shown in SEQ ID NO: 199, and CDR-L3 shown in SEQ ID NO: 200. Accordingly, the present invention provides a polypeptide / polypeptide construct comprising a domain that (immunoselectively) binds to an epitope recognized by a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 195, CDR-H2 shown in SEQ ID NO: 196, and CDR-H3 shown in SEQ ID NO: 197, and a VL region including CDR-L1 shown in SEQ ID NO: 198, CDR-L2 shown in SEQ ID NO: 199, and CDR-L3 shown in SEQ ID NO: 200.

[0026] The present invention provides a polypeptide / polypeptide construct comprising a domain containing a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope recognized by a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 237, CDR-H2 shown in SEQ ID NO: 238, and CDR-H3 shown in SEQ ID NO: 239, and a VL region including CDR-L1 shown in SEQ ID NO: 240, CDR-L2 shown in SEQ ID NO: 241, and CDR-L3 shown in SEQ ID NO: 242. Accordingly, the present invention provides a polypeptide / polypeptide construct comprising a domain that (immunoselectively) binds to an epitope recognized by a domain comprising a VH region including CDR-H1 shown in SEQ ID NO: 237, CDR-H2 shown in SEQ ID NO: 238, and CDR-H3 shown in SEQ ID NO: 239, and a VL region including CDR-L1 shown in SEQ ID NO: 240, CDR-L2 shown in SEQ ID NO: 241, and CDR-L3 shown in SEQ ID NO: 242.

[0027] According to the present invention, polypeptides / polypeptide constructs are provided, where, (i) The domain contains a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope region containing amino acids of the first extracellular loop of CLDN6 (as listed in Sequence ID No. 1), also known as extracellular loop 1 (ECL1), the epitope region shown in Sequence ID No. 9, and optionally contains one of the sequences referred to in a) to s) below, and / or (ii) The domain contains a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope region containing amino acids of the second extracellular loop of CLDN6 (as listed in Sequence ID No. 1), also known as extracellular loop 2 (ECL2), the epitope region shown in Sequence ID No. 10, and optionally contains one of the sequences referred to in a) to s) below, and / or (iii) The domain (immunoselectively) binds to an epitope region of CLDN6 containing amino acids of ECL1 and ECL2, preferably an epitope region containing amino acids of SEQ ID NOs. 9 and 10, and includes a paratope (antigen-binding (epitope-binding) structure) which may include any one of the structures referred to in a) to s) below, and / or (iv) The domain contains a paratope (antigen-binding (epitope-binding) structure) that binds to CLDN6 on the surface of target cells and (immunoselectively) to the same CLDN6 epitope as an antibody or polypeptide construct containing a paratope containing any one of the sequences mentioned in a) to s) below: a) The VH region including CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and the VL region including CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO: 18; b) The VH region including CDR-H1 shown in SEQ ID NO: 27, CDR-H2 shown in SEQ ID NO: 28, and CDR-H3 shown in SEQ ID NO: 29, and the VL region including CDR-L1 shown in SEQ ID NO: 30, CDR-L2 shown in SEQ ID NO: 31, and CDR-L3 shown in SEQ ID NO: 32; c) The VH region including CDR-H1 shown in SEQ ID NO: 41, CDR-H2 shown in SEQ ID NO: 42, and CDR-H3 shown in SEQ ID NO: 43, and the VL region including CDR-L1 shown in SEQ ID NO: 44, CDR-L2 shown in SEQ ID NO: 45, and CDR-L3 shown in SEQ ID NO: 46; d) The VH region including CDR-H1 shown in SEQ ID NO: 55, CDR-H2 shown in SEQ ID NO: 56, and CDR-H3 shown in SEQ ID NO: 57, and the VL region including CDR-L1 shown in SEQ ID NO: 58, CDR-L2 shown in SEQ ID NO: 59, and CDR-L3 shown in SEQ ID NO: 60; e) The VH region including CDR-H1 shown in SEQ ID NO: 69, CDR-H2 shown in SEQ ID NO: 70, and CDR-H3 shown in SEQ ID NO: 71, and the VL region including CDR-L1 shown in SEQ ID NO: 72, CDR-L2 shown in SEQ ID NO: 73, and CDR-L3 shown in SEQ ID NO: 74; f) The VH region including CDR-H1 shown in SEQ ID NO: 83, CDR-H2 shown in SEQ ID NO: 84, and CDR-H3 shown in SEQ ID NO: 85, and the VL region including CDR-L1 shown in SEQ ID NO: 86, CDR-L2 shown in SEQ ID NO: 87, and CDR-L3 shown in SEQ ID NO: 88; g) The VH region including CDR-H1 shown in SEQ ID NO: 97, CDR-H2 shown in SEQ ID NO: 98, and CDR-H3 shown in SEQ ID NO: 99, and the VL region including CDR-L1 shown in SEQ ID NO: 100, CDR-L2 shown in SEQ ID NO: 101, and CDR-L3 shown in SEQ ID NO: 102; h) A VH region including CDR-H1 shown in SEQ ID NO: 111, CDR-H2 shown in SEQ ID NO: 112, and CDR-H3 shown in SEQ ID NO: 113, and a VL region including CDR-L1 shown in SEQ ID NO: 114, CDR-L2 shown in SEQ ID NO: 115, and CDR-L3 shown in SEQ ID NO: 116; i) The VH region including CDR-H1 shown in SEQ ID NO: 125, CDR-H2 shown in SEQ ID NO: 126, and CDR-H3 shown in SEQ ID NO: 127, and the VL region including CDR-L1 shown in SEQ ID NO: 128, CDR-L2 shown in SEQ ID NO: 129, and CDR-L3 shown in SEQ ID NO: 130; j) The VH region including CDR-H1 shown in SEQ ID NO: 139, CDR-H2 shown in SEQ ID NO: 140, and CDR-H3 shown in SEQ ID NO: 141, and the VL region including CDR-L1 shown in SEQ ID NO: 142, CDR-L2 shown in SEQ ID NO: 143, and CDR-L3 shown in SEQ ID NO: 144; k) The VH region including CDR-H1 shown in SEQ ID NO: 153, CDR-H2 shown in SEQ ID NO: 154, and CDR-H3 shown in SEQ ID NO: 155, and the VL region including CDR-L1 shown in SEQ ID NO: 156, CDR-L2 shown in SEQ ID NO: 157, and CDR-L3 shown in SEQ ID NO: 158; l) The VH region including CDR-H1 shown in SEQ ID NO: 167, CDR-H2 shown in SEQ ID NO: 168, and CDR-H3 shown in SEQ ID NO: 169, and the VL region including CDR-L1 shown in SEQ ID NO: 170, CDR-L2 shown in SEQ ID NO: 171, and CDR-L3 shown in SEQ ID NO: 172; m) The VH region including CDR-H1 shown in SEQ ID NO: 181, CDR-H2 shown in SEQ ID NO: 182, and CDR-H3 shown in SEQ ID NO: 183, and the VL region including CDR-L1 shown in SEQ ID NO: 184, CDR-L2 shown in SEQ ID NO: 185, and CDR-L3 shown in SEQ ID NO: 186; n) The VH region including CDR-H1 shown in SEQ ID NO: 195, CDR-H2 shown in SEQ ID NO: 196, and CDR-H3 shown in SEQ ID NO: 197, and the VL region including CDR-L1 shown in SEQ ID NO: 198, CDR-L2 shown in SEQ ID NO: 199, and CDR-L3 shown in SEQ ID NO: 200; o) The VH region including CDR-H1 shown in SEQ ID NO: 209, CDR-H2 shown in SEQ ID NO: 210, and CDR-H3 shown in SEQ ID NO: 211, and the VL region including CDR-L1 shown in SEQ ID NO: 212, CDR-L2 shown in SEQ ID NO: 213, and CDR-L3 shown in SEQ ID NO: 214; p) The VH region including CDR-H1 shown in SEQ ID NO: 223, CDR-H2 shown in SEQ ID NO: 224, and CDR-H3 shown in SEQ ID NO: 225, and the VL region including CDR-L1 shown in SEQ ID NO: 226, CDR-L2 shown in SEQ ID NO: 227, and CDR-L3 shown in SEQ ID NO: 228; q) The VH region including CDR-H1 shown in SEQ ID NO: 237, CDR-H2 shown in SEQ ID NO: 238, and CDR-H3 shown in SEQ ID NO: 239, and the VL region including CDR-L1 shown in SEQ ID NO: 240, CDR-L2 shown in SEQ ID NO: 241, and CDR-L3 shown in SEQ ID NO: 242; r) The VH region including CDR-H1 shown in SEQ ID NO: 251, CDR-H2 shown in SEQ ID NO: 252, and CDR-H3 shown in SEQ ID NO: 253, and the VL region including CDR-L1 shown in SEQ ID NO: 254, CDR-L2 shown in SEQ ID NO: 255, and CDR-L3 shown in SEQ ID NO: 256; and s) A VH region including CDR-H1 shown in SEQ ID NO: 265, CDR-H2 shown in SEQ ID NO: 266, and CDR-H3 shown in SEQ ID NO: 267, and a VL region including CDR-L1 shown in SEQ ID NO: 268, CDR-L2 shown in SEQ ID NO: 269, and CDR-L3 shown in SEQ ID NO: 270.

[0028] Therefore, according to the present invention, polypeptides / polypeptide constructs are provided, where, (i) A domain that (immunoselectively) binds to the amino acid-containing epitope region of the first extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 1 (ECL1), the epitope region shown in SEQ ID NO: 9, and / or optionally contains one of the sequences referred to in a) to s) below, and / or (ii) A domain that (immunoselectively) binds to the epitope region containing amino acids of the second extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 2 (ECL2), which is shown in SEQ ID NO: 10 and may contain any one of the sequences referred to in a) to s) below, and / or (iii) A domain that (immunoselectively) binds to the epitope region of CLDN6 containing the amino acids of ECL1 and ECL2, preferably the epitope region containing the amino acids of SEQ ID NOs. 9 and 10, and optionally includes any one of the structures referred to in a) to s) below, and / or (iv) Domains that bind to CLDN6 on the surface of target cells and (immunoselectively) bind to the same CLDN6 epitope as an antibody or polypeptide construct containing a paratope containing any one of the sequences mentioned in a) to s) below: a) The VH region including CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and the VL region including CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO: 18; b) The VH region including CDR-H1 shown in SEQ ID NO: 27, CDR-H2 shown in SEQ ID NO: 28, and CDR-H3 shown in SEQ ID NO: 29, and the VL region including CDR-L1 shown in SEQ ID NO: 30, CDR-L2 shown in SEQ ID NO: 31, and CDR-L3 shown in SEQ ID NO: 32; c) The VH region including CDR-H1 shown in SEQ ID NO: 41, CDR-H2 shown in SEQ ID NO: 42, and CDR-H3 shown in SEQ ID NO: 43, and the VL region including CDR-L1 shown in SEQ ID NO: 44, CDR-L2 shown in SEQ ID NO: 45, and CDR-L3 shown in SEQ ID NO: 46; d) The VH region including CDR-H1 shown in SEQ ID NO: 55, CDR-H2 shown in SEQ ID NO: 56, and CDR-H3 shown in SEQ ID NO: 57, and the VL region including CDR-L1 shown in SEQ ID NO: 58, CDR-L2 shown in SEQ ID NO: 59, and CDR-L3 shown in SEQ ID NO: 60; e) The VH region including CDR-H1 shown in SEQ ID NO: 69, CDR-H2 shown in SEQ ID NO: 70, and CDR-H3 shown in SEQ ID NO: 71, and the VL region including CDR-L1 shown in SEQ ID NO: 72, CDR-L2 shown in SEQ ID NO: 73, and CDR-L3 shown in SEQ ID NO: 74; f) The VH region including CDR-H1 shown in SEQ ID NO: 83, CDR-H2 shown in SEQ ID NO: 84, and CDR-H3 shown in SEQ ID NO: 85, and the VL region including CDR-L1 shown in SEQ ID NO: 86, CDR-L2 shown in SEQ ID NO: 87, and CDR-L3 shown in SEQ ID NO: 88; g) The VH region including CDR-H1 shown in SEQ ID NO: 97, CDR-H2 shown in SEQ ID NO: 98, and CDR-H3 shown in SEQ ID NO: 99, and the VL region including CDR-L1 shown in SEQ ID NO: 100, CDR-L2 shown in SEQ ID NO: 101, and CDR-L3 shown in SEQ ID NO: 102; h) A VH region including CDR-H1 shown in SEQ ID NO: 111, CDR-H2 shown in SEQ ID NO: 112, and CDR-H3 shown in SEQ ID NO: 113, and a VL region including CDR-L1 shown in SEQ ID NO: 114, CDR-L2 shown in SEQ ID NO: 115, and CDR-L3 shown in SEQ ID NO: 116; i) The VH region including CDR-H1 shown in SEQ ID NO: 125, CDR-H2 shown in SEQ ID NO: 126, and CDR-H3 shown in SEQ ID NO: 127, and the VL region including CDR-L1 shown in SEQ ID NO: 128, CDR-L2 shown in SEQ ID NO: 129, and CDR-L3 shown in SEQ ID NO: 130; j) The VH region including CDR-H1 shown in SEQ ID NO: 139, CDR-H2 shown in SEQ ID NO: 140, and CDR-H3 shown in SEQ ID NO: 141, and the VL region including CDR-L1 shown in SEQ ID NO: 142, CDR-L2 shown in SEQ ID NO: 143, and CDR-L3 shown in SEQ ID NO: 144; k) The VH region including CDR-H1 shown in SEQ ID NO: 153, CDR-H2 shown in SEQ ID NO: 154, and CDR-H3 shown in SEQ ID NO: 155, and the VL region including CDR-L1 shown in SEQ ID NO: 156, CDR-L2 shown in SEQ ID NO: 157, and CDR-L3 shown in SEQ ID NO: 158; l) The VH region including CDR-H1 shown in SEQ ID NO: 167, CDR-H2 shown in SEQ ID NO: 168, and CDR-H3 shown in SEQ ID NO: 169, and the VL region including CDR-L1 shown in SEQ ID NO: 170, CDR-L2 shown in SEQ ID NO: 171, and CDR-L3 shown in SEQ ID NO: 172; m) The VH region including CDR-H1 shown in SEQ ID NO: 181, CDR-H2 shown in SEQ ID NO: 182, and CDR-H3 shown in SEQ ID NO: 183, and the VL region including CDR-L1 shown in SEQ ID NO: 184, CDR-L2 shown in SEQ ID NO: 185, and CDR-L3 shown in SEQ ID NO: 186; n) The VH region including CDR-H1 shown in SEQ ID NO: 195, CDR-H2 shown in SEQ ID NO: 196, and CDR-H3 shown in SEQ ID NO: 197, and the VL region including CDR-L1 shown in SEQ ID NO: 198, CDR-L2 shown in SEQ ID NO: 199, and CDR-L3 shown in SEQ ID NO: 200; o) The VH region including CDR-H1 shown in SEQ ID NO: 209, CDR-H2 shown in SEQ ID NO: 210, and CDR-H3 shown in SEQ ID NO: 211, and the VL region including CDR-L1 shown in SEQ ID NO: 212, CDR-L2 shown in SEQ ID NO: 213, and CDR-L3 shown in SEQ ID NO: 214; p) The VH region including CDR-H1 shown in SEQ ID NO: 223, CDR-H2 shown in SEQ ID NO: 224, and CDR-H3 shown in SEQ ID NO: 225, and the VL region including CDR-L1 shown in SEQ ID NO: 226, CDR-L2 shown in SEQ ID NO: 227, and CDR-L3 shown in SEQ ID NO: 228; q) The VH region including CDR-H1 shown in SEQ ID NO: 237, CDR-H2 shown in SEQ ID NO: 238, and CDR-H3 shown in SEQ ID NO: 239, and the VL region including CDR-L1 shown in SEQ ID NO: 240, CDR-L2 shown in SEQ ID NO: 241, and CDR-L3 shown in SEQ ID NO: 242; r) The VH region including CDR-H1 shown in SEQ ID NO: 251, CDR-H2 shown in SEQ ID NO: 252, and CDR-H3 shown in SEQ ID NO: 253, and the VL region including CDR-L1 shown in SEQ ID NO: 254, CDR-L2 shown in SEQ ID NO: 255, and CDR-L3 shown in SEQ ID NO: 256; and s) A VH region including CDR-H1 shown in SEQ ID NO: 265, CDR-H2 shown in SEQ ID NO: 266, and CDR-H3 shown in SEQ ID NO: 267, and a VL region including CDR-L1 shown in SEQ ID NO: 268, CDR-L2 shown in SEQ ID NO: 269, and CDR-L3 shown in SEQ ID NO: 270.

[0029] According to the present invention, polypeptides / polypeptide constructs are provided, in which, (i) The domain contains a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope region containing amino acids of the first extracellular loop of CLDN6 (as listed in Sequence ID No. 1), also known as extracellular loop 1 (ECL1), the epitope region shown in Sequence ID No. 9, and optionally contains one of the sequences referred to in a-1) to s-1) below, and / or (ii) The domain contains a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope region containing amino acids of the second extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 2 (ECL2), the epitope region shown in SEQ ID NO: 10, and optionally contains one of the sequences referred to in a-1) to s-1) below, and / or (iii) The domain (immunoselectively) binds to the epitope region of CLDN6 containing the amino acids of ECL1 and ECL2, preferably the epitope region containing the amino acids of SEQ ID NOs. 9 and 10, and includes a paratope (antigen-binding (epitope-binding) structure) which may include any one of the structures referred to in a-1) to s-1) below, and / or (iv) The domain contains a paratope (antigen-binding (epitope-binding) structure) that binds to CLDN6 on the surface of target cells and (immunoselectively) to the same CLDN6 epitope as an antibody or polypeptide construct containing a paratope containing any one of the sequences mentioned in a-1) to s-1) below: a-1) The VH region shown in Sequence ID No. 11 and / or the VL region shown in Sequence ID No. 12; b-1) The VH region shown in Sequence ID No. 25 and / or the VL region shown in Sequence ID No. 26; c-1) The VH region shown in Sequence ID No. 39 and / or the VL region shown in Sequence ID No. 40; d-1) The VH region shown in Sequence ID No. 53 and / or the VL region shown in Sequence ID No. 54; e-1) The VH region shown in Sequence ID No. 67 and / or the VL region shown in Sequence ID No. 68; f-1) The VH region shown in Sequence ID 81 and / or the VL region shown in Sequence ID 82; g-1) The VH region shown in Sequence ID No. 95 and / or the VL region shown in Sequence ID No. 96; h-1) The VH region shown in Sequence ID No. 109 and / or the VL region shown in Sequence ID No. 110; i-1) The VH region shown in Sequence ID No. 123 and / or the VL region shown in Sequence ID No. 124; j-1) The VH region shown in Sequence ID No. 137 and / or the VL region shown in Sequence ID No. 138; k-1) The VH region shown in Sequence ID No. 151 and / or the VL region shown in Sequence ID No. 152; l-1) The VH region shown in Sequence ID No. 165 and / or the VL region shown in Sequence ID No. 166; m-1) The VH region shown in Sequence ID No. 179 and / or the VL region shown in Sequence ID No. 180; n-1) The VH region shown in sequence number 193 and / or the VL region shown in sequence number 194; o-1) The VH region shown in Sequence ID No. 207 and / or the VL region shown in Sequence ID No. 208; p-1) The VH region shown in Sequence ID No. 221 and / or the VL region shown in Sequence ID No. 222; q-1) The VH region shown in Sequence ID No. 235 and / or the VL region shown in Sequence ID No. 236; r-1) The VH region shown in Sequence ID No. 249 and / or the VL region shown in Sequence ID No. 250; and s-1) The VH region shown in Sequence ID No. 263 and / or the VL region shown in Sequence ID No. 264.

[0030] Therefore, according to the present invention, polypeptides / polypeptide constructs are provided, where, (i) A domain that (immunoselectively) binds to the amino acid-containing epitope region of the first extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 1 (ECL1), the epitope region shown in SEQ ID NO: 9, and / or optionally contains one of the sequences referred to in a-1) to s-1) below, and / or (ii) A domain that (immunoselectively) binds to the epitope region containing amino acids of the second extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 2 (ECL2), which is shown in SEQ ID NO: 10 and may contain one of the sequences referred to in a-1) to s-1) below, and / or (iii) A domain that (immunoselectively) binds to the epitope region of CLDN6 containing the amino acids of ECL1 and ECL2, preferably the epitope region containing the amino acids of SEQ ID NOs. 9 and 10, and optionally includes one of the structures referred to in a-1) to s-1) below, and / or (iv) Domains that bind to CLDN6 on the surface of target cells and (immunoselectively) bind to the same CLDN6 epitope as an antibody or polypeptide construct containing a paratope containing any one of the sequences mentioned in a-1) to s-1) below: a-1) The VH region shown in Sequence ID No. 11 and / or the VL region shown in Sequence ID No. 12; b-1) The VH region shown in Sequence ID No. 25 and / or the VL region shown in Sequence ID No. 26; c-1) The VH region shown in Sequence ID No. 39 and / or the VL region shown in Sequence ID No. 40; d-1) The VH region shown in Sequence ID No. 53 and / or the VL region shown in Sequence ID No. 54; e-1) The VH region shown in Sequence ID No. 67 and / or the VL region shown in Sequence ID No. 68; f-1) The VH region shown in Sequence ID 81 and / or the VL region shown in Sequence ID 82; g-1) The VH region shown in Sequence ID No. 95 and / or the VL region shown in Sequence ID No. 96; h-1) The VH region shown in Sequence ID No. 109 and / or the VL region shown in Sequence ID No. 110; i-1) The VH region shown in Sequence ID No. 123 and / or the VL region shown in Sequence ID No. 124; j-1) The VH region shown in Sequence ID No. 137 and / or the VL region shown in Sequence ID No. 138; k-1) The VH region shown in Sequence ID No. 151 and / or the VL region shown in Sequence ID No. 152; l-1) The VH region shown in Sequence ID No. 165 and / or the VL region shown in Sequence ID No. 166; m-1) The VH region shown in Sequence ID No. 179 and / or the VL region shown in Sequence ID No. 180; n-1) The VH region shown in sequence number 193 and / or the VL region shown in sequence number 194; o-1) The VH region shown in Sequence ID No. 207 and / or the VL region shown in Sequence ID No. 208; p-1) The VH region shown in Sequence ID No. 221 and / or the VL region shown in Sequence ID No. 222; q-1) The VH region shown in Sequence ID No. 235 and / or the VL region shown in Sequence ID No. 236; r-1) The VH region shown in Sequence ID No. 249 and / or the VL region shown in Sequence ID No. 250; and s-1) The VH region shown in Sequence ID No. 263 and / or the VL region shown in Sequence ID No. 264.

[0031] The present invention provides polypeptide / polypeptide constructs that compete for binding with polypeptide constructs containing or consisting of domains. (i) The domain contains a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope region containing amino acids of the first extracellular loop of CLDN6 (as listed in Sequence ID No. 1), also known as extracellular loop 1 (ECL1), the epitope region shown in Sequence ID No. 9, and optionally contains one of the sequences referred to in a-1) to s-1) below, and / or (ii) The domain contains a paratope (antigen-binding (epitope-binding) structure) that (immunoselectively) binds to an epitope region containing amino acids of the second extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 2 (ECL2), the epitope region shown in SEQ ID NO: 10, and optionally contains one of the sequences referred to in a-1) to s-1) below, and / or (iii) The domain (immunoselectively) binds to the epitope region of CLDN6 containing the amino acids of ECL1 and ECL2, preferably the epitope region containing the amino acids of SEQ ID NOs. 9 and 10, and includes a paratope (antigen-binding (epitope-binding) structure) which may include any one of the structures referred to in a-1) to s-1) below, and / or (iv) The domain contains a paratope (antigen-binding (epitope-binding) structure) that binds to CLDN6 on the surface of target cells and (immunoselectively) to the same CLDN6 epitope as an antibody or polypeptide construct containing a paratope containing any one of the sequences mentioned in a-1) to s-1) below: a-1) The VH region shown in Sequence ID No. 11 and / or the VL region shown in Sequence ID No. 12; b-1) The VH region shown in Sequence ID No. 25 and / or the VL region shown in Sequence ID No. 26; c-1) The VH region shown in Sequence ID No. 39 and / or the VL region shown in Sequence ID No. 40; d-1) The VH region shown in Sequence ID No. 53 and / or the VL region shown in Sequence ID No. 54; e-1) The VH region shown in Sequence ID No. 67 and / or the VL region shown in Sequence ID No. 68; f-1) The VH region shown in Sequence ID 81 and / or the VL region shown in Sequence ID 82; g-1) The VH region shown in Sequence ID No. 95 and / or the VL region shown in Sequence ID No. 96; h-1) The VH region shown in Sequence ID No. 109 and / or the VL region shown in Sequence ID No. 110; i-1) The VH region shown in Sequence ID No. 123 and / or the VL region shown in Sequence ID No. 124; j-1) The VH region shown in Sequence ID No. 137 and / or the VL region shown in Sequence ID No. 138; k-1) The VH region shown in Sequence ID No. 151 and / or the VL region shown in Sequence ID No. 152; l-1) The VH region shown in Sequence ID No. 165 and / or the VL region shown in Sequence ID No. 166; m-1) The VH region shown in Sequence ID No. 179 and / or the VL region shown in Sequence ID No. 180; n-1) The VH region shown in sequence number 193 and / or the VL region shown in sequence number 194; o-1) The VH region shown in Sequence ID No. 207 and / or the VL region shown in Sequence ID No. 208; p-1) The VH region shown in Sequence ID No. 221 and / or the VL region shown in Sequence ID No. 222; q-1) The VH region shown in Sequence ID No. 235 and / or the VL region shown in Sequence ID No. 236; r-1) The VH region shown in Sequence ID No. 249 and / or the VL region shown in Sequence ID No. 250; and s-1) The VH region shown in Sequence ID No. 263 and / or the VL region shown in Sequence ID No. 264.

[0032] Therefore, the present invention provides polypeptide / polypeptide constructs that compete for binding with polypeptide constructs that include or consist of domains. (i) A domain that (immunoselectively) binds to the amino acid-containing epitope region of the first extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 1 (ECL1), the epitope region shown in SEQ ID NO: 9, and / or optionally contains one of the sequences referred to in a-1) to s-1) below, and / or (ii) A domain that (immunoselectively) binds to the epitope region containing amino acids of the second extracellular loop of CLDN6 (as listed in SEQ ID NO: 1), also known as extracellular loop 2 (ECL2), which is shown in SEQ ID NO: 10 and may contain one of the sequences referred to in a-1) to s-1) below, and / or (iii) A domain that (immunoselectively) binds to the epitope region of CLDN6 containing the amino acids of ECL1 and ECL2, preferably the epitope region containing the amino acids of SEQ ID NOs. 9 and 10, and optionally includes one of the structures referred to in a-1) to s-1) below, and / or (iv) Domains that bind to CLDN6 on the surface of target cells and (immunoselectively) bind to the same CLDN6 epitope as an antibody or polypeptide construct containing a paratope containing any one of the sequences mentioned in a-1) to s-1) below: a-1) The VH region shown in Sequence ID No. 11 and / or the VL region shown in Sequence ID No. 12; b-1) The VH region shown in Sequence ID No. 25 and / or the VL region shown in Sequence ID No. 26; c-1) The VH region shown in Sequence ID No. 39 and / or the VL region shown in Sequence ID No. 40; d-1) The VH region shown in Sequence ID No. 53 and / or the VL region shown in Sequence ID No. 54; e-1) The VH region shown in Sequence ID No. 67 and / or the VL region shown in Sequence ID No. 68; f-1) The VH region shown in Sequence ID 81 and / or the VL region shown in Sequence ID 82; g-1) The VH region shown in Sequence ID No. 95 and / or the VL region shown in Sequence ID No. 96; h-1) The VH region shown in Sequence ID No. 109 and / or the VL region shown in Sequence ID No. 110; i-1) The VH region shown in Sequence ID No. 123 and / or the VL region shown in Sequence ID No. 124; j-1) The VH region shown in Sequence ID No. 137 and / or the VL region shown in Sequence ID No. 138; k-1) The VH region shown in Sequence ID No. 151 and / or the VL region shown in Sequence ID No. 152; l-1) The VH region shown in Sequence ID No. 165 and / or the VL region shown in Sequence ID No. 166; m-1) The VH region shown in Sequence ID No. 179 and / or the VL region shown in Sequence ID No. 180; n-1) The VH region shown in sequence number 193 and / or the VL region shown in sequence number 194; o-1) The VH region shown in Sequence ID No. 207 and / or the VL region shown in Sequence ID No. 208; p-1) The VH region shown in Sequence ID No. 221 and / or the VL region shown in Sequence ID No. 222; q-1) The VH region shown in Sequence ID No. 235 and / or the VL region shown in Sequence ID No. 236; r-1) The VH region shown in Sequence ID No. 249 and / or the VL region shown in Sequence ID No. 250; and s-1) The VH region shown in Sequence ID No. 263 and / or the VL region shown in Sequence ID No. 264.

[0033] Furthermore, the polypeptide constructs of the present invention selectively bind to CLDN6 on the surface of target cells and compete for binding with constructs containing a domain comprising any one of the sequences mentioned in a) to s) below, with a) to d), n), and s), being preferred, and a) to c), e), and s), being particularly preferred. a) The VH region including CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and the VL region including CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO: 18; b) The VH region including CDR-H1 shown in SEQ ID NO: 27, CDR-H2 shown in SEQ ID NO: 28, and CDR-H3 shown in SEQ ID NO: 29, and the VL region including CDR-L1 shown in SEQ ID NO: 30, CDR-L2 shown in SEQ ID NO: 31, and CDR-L3 shown in SEQ ID NO: 32; c) The VH region including CDR-H1 shown in SEQ ID NO: 41, CDR-H2 shown in SEQ ID NO: 42, and CDR-H3 shown in SEQ ID NO: 43, and the VL region including CDR-L1 shown in SEQ ID NO: 44, CDR-L2 shown in SEQ ID NO: 45, and CDR-L3 shown in SEQ ID NO: 46; d) The VH region including CDR-H1 shown in SEQ ID NO: 55, CDR-H2 shown in SEQ ID NO: 56, and CDR-H3 shown in SEQ ID NO: 57, and the VL region including CDR-L1 shown in SEQ ID NO: 58, CDR-L2 shown in SEQ ID NO: 59, and CDR-L3 shown in SEQ ID NO: 60; e) The VH region including CDR-H1 shown in SEQ ID NO: 69, CDR-H2 shown in SEQ ID NO: 70, and CDR-H3 shown in SEQ ID NO: 71, and the VL region including CDR-L1 shown in SEQ ID NO: 72, CDR-L2 shown in SEQ ID NO: 73, and CDR-L3 shown in SEQ ID NO: 74; f) The VH region including CDR-H1 shown in SEQ ID NO: 83, CDR-H2 shown in SEQ ID NO: 84, and CDR-H3 shown in SEQ ID NO: 85, and the VL region including CDR-L1 shown in SEQ ID NO: 86, CDR-L2 shown in SEQ ID NO: 87, and CDR-L3 shown in SEQ ID NO: 88; g) The VH region including CDR-H1 shown in SEQ ID NO: 97, CDR-H2 shown in SEQ ID NO: 98, and CDR-H3 shown in SEQ ID NO: 99, and the VL region including CDR-L1 shown in SEQ ID NO: 100, CDR-L2 shown in SEQ ID NO: 101, and CDR-L3 shown in SEQ ID NO: 102; h) A VH region including CDR-H1 shown in SEQ ID NO: 111, CDR-H2 shown in SEQ ID NO: 112, and CDR-H3 shown in SEQ ID NO: 113, and a VL region including CDR-L1 shown in SEQ ID NO: 114, CDR-L2 shown in SEQ ID NO: 115, and CDR-L3 shown in SEQ ID NO: 116; i) The VH region including CDR-H1 shown in SEQ ID NO: 125, CDR-H2 shown in SEQ ID NO: 126, and CDR-H3 shown in SEQ ID NO: 127, and the VL region including CDR-L1 shown in SEQ ID NO: 128, CDR-L2 shown in SEQ ID NO: 129, and CDR-L3 shown in SEQ ID NO: 130; j) The VH region including CDR-H1 shown in SEQ ID NO: 139, CDR-H2 shown in SEQ ID NO: 140, and CDR-H3 shown in SEQ ID NO: 141, and the VL region including CDR-L1 shown in SEQ ID NO: 142, CDR-L2 shown in SEQ ID NO: 143, and CDR-L3 shown in SEQ ID NO: 144; k) The VH region including CDR-H1 shown in SEQ ID NO: 153, CDR-H2 shown in SEQ ID NO: 154, and CDR-H3 shown in SEQ ID NO: 155, and the VL region including CDR-L1 shown in SEQ ID NO: 156, CDR-L2 shown in SEQ ID NO: 157, and CDR-L3 shown in SEQ ID NO: 158; l) The VH region including CDR-H1 shown in SEQ ID NO: 167, CDR-H2 shown in SEQ ID NO: 168, and CDR-H3 shown in SEQ ID NO: 169, and the VL region including CDR-L1 shown in SEQ ID NO: 170, CDR-L2 shown in SEQ ID NO: 171, and CDR-L3 shown in SEQ ID NO: 172; m) The VH region including CDR-H1 shown in SEQ ID NO: 181, CDR-H2 shown in SEQ ID NO: 182, and CDR-H3 shown in SEQ ID NO: 183, and the VL region including CDR-L1 shown in SEQ ID NO: 184, CDR-L2 shown in SEQ ID NO: 185, and CDR-L3 shown in SEQ ID NO: 186; n) The VH region including CDR-H1 shown in SEQ ID NO: 195, CDR-H2 shown in SEQ ID NO: 196, and CDR-H3 shown in SEQ ID NO: 197, and the VL region including CDR-L1 shown in SEQ ID NO: 198, CDR-L2 shown in SEQ ID NO: 199, and CDR-L3 shown in SEQ ID NO: 200; o) The VH region including CDR-H1 shown in SEQ ID NO: 209, CDR-H2 shown in SEQ ID NO: 210, and CDR-H3 shown in SEQ ID NO: 211, and the VL region including CDR-L1 shown in SEQ ID NO: 212, CDR-L2 shown in SEQ ID NO: 213, and CDR-L3 shown in SEQ ID NO: 214; p) The VH region including CDR-H1 shown in SEQ ID NO: 223, CDR-H2 shown in SEQ ID NO: 224, and CDR-H3 shown in SEQ ID NO: 225, and the VL region including CDR-L1 shown in SEQ ID NO: 226, CDR-L2 shown in SEQ ID NO: 227, and CDR-L3 shown in SEQ ID NO: 228; q) The VH region including CDR-H1 shown in SEQ ID NO: 237, CDR-H2 shown in SEQ ID NO: 238, and CDR-H3 shown in SEQ ID NO: 239, and the VL region including CDR-L1 shown in SEQ ID NO: 240, CDR-L2 shown in SEQ ID NO: 241, and CDR-L3 shown in SEQ ID NO: 242; r) The VH region including CDR-H1 shown in SEQ ID NO: 251, CDR-H2 shown in SEQ ID NO: 252, and CDR-H3 shown in SEQ ID NO: 253, and the VL region including CDR-L1 shown in SEQ ID NO: 254, CDR-L2 shown in SEQ ID NO: 255, and CDR-L3 shown in SEQ ID NO: 256; and s) A VH region including CDR-H1 shown in SEQ ID NO: 265, CDR-H2 shown in SEQ ID NO: 266, and CDR-H3 shown in SEQ ID NO: 267, and a VL region including CDR-L1 shown in SEQ ID NO: 268, CDR-L2 shown in SEQ ID NO: 269, and CDR-L3 shown in SEQ ID NO: 270.

[0034] Furthermore, the polypeptide constructs of the present invention bind (immunoselectively) to CLDN6 on the surface of target cells and bind to or compete for binding with antibodies or polypeptide constructs containing a paratope (i.e., an antigen-binding or epitope-binding structure) that includes any one of the group of sequences, and the polypeptide constructs of the present invention bind (immunoselectively) to CLDN6 on the surface of target cells and bind to or compete for binding with antibodies or polypeptide constructs containing any one of the group of sequences. a-1) The VH region shown in Sequence ID No. 11 and / or the VL region shown in Sequence ID No. 12; b-1) The VH region shown in Sequence ID No. 25 and / or the VL region shown in Sequence ID No. 26; c-1) The VH region shown in Sequence ID No. 39 and / or the VL region shown in Sequence ID No. 40; d-1) The VH region shown in Sequence ID No. 53 and / or the VL region shown in Sequence ID No. 54; e-1) The VH region shown in Sequence ID No. 67 and / or the VL region shown in Sequence ID No. 68; f-1) The VH region shown in Sequence ID 81 and / or the VL region shown in Sequence ID 82; g-1) The VH region shown in Sequence ID No. 95 and / or the VL region shown in Sequence ID No. 96; h-1) The VH region shown in Sequence ID No. 109 and / or the VL region shown in Sequence ID No. 110; i-1) The VH region shown in Sequence ID No. 123 and / or the VL region shown in Sequence ID No. 124; j-1) The VH region shown in Sequence ID No. 137 and / or the VL region shown in Sequence ID No. 138; k-1) The VH region shown in Sequence ID No. 151 and / or the VL region shown in Sequence ID No. 152; l-1) The VH region shown in Sequence ID No. 165 and / or the VL region shown in Sequence ID No. 166; m-1) The VH region shown in Sequence ID No. 179 and / or the VL region shown in Sequence ID No. 180; n-1) The VH region shown in sequence number 193 and / or the VL region shown in sequence number 194; o-1) The VH region shown in Sequence ID No. 207 and / or the VL region shown in Sequence ID No. 208; p-1) The VH region shown in Sequence ID No. 221 and / or the VL region shown in Sequence ID No. 222; q-1) The VH region shown in Sequence ID No. 235 and / or the VL region shown in Sequence ID No. 236; r-1) The VH region shown in Sequence ID No. 249 and / or the VL region shown in Sequence ID No. 250; and s-1) The VH region shown in Sequence ID No. 263 and / or the VL region shown in Sequence ID No. 264.

[0035] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, wherein the paratope (i.e., antigen-binding (epitope-binding) structure) that binds to CLDN6 is composed of a pair of VH and VL regions, and the domain that binds to CLDN6 is one of the following: SEQ ID NOs: 11+12, 25+26, 39+40, 53+54, 67+68, 81+82, 95+96, 109+110, 123+124, 137+138, The present invention relates to a polypeptide / polypeptide construct described in any one of the preceding paragraphs, comprising a pair of VH and VL regions that includes the amino acid sequence shown in sequence number 151+152, sequence number 165+166, sequence number 179+180, sequence number 193+194, sequence number 207+208, sequence number 221+222, sequence number 235+236, sequence number 249+250, or sequence number 263+264, or competes with a polypeptide construct that binds to CLDN6.

[0036] The present invention relates to polypeptide / polypeptide constructs described in any one of the preceding paragraphs, which compete with polypeptide constructs comprising, or consisting of, the amino acid sequences shown in SEQ ID NO: 19, SEQ ID NO: 22, SEQ ID NO: 33, SEQ ID NO: 36, SEQ ID NO: 47, SEQ ID NO: 50, SEQ ID NO: 61, SEQ ID NO: 64, SEQ ID NO: 75, SEQ ID NO: 78, SEQ ID NO: 89, SEQ ID NO: 92, SEQ ID NO: 103, SEQ ID NO: 106, SEQ ID NO: 117, SEQ ID NO: 120, SEQ ID NO: 131, SEQ ID NO: 134, SEQ ID NO: 145, SEQ ID NO: 148, SEQ ID NO: 159, SEQ ID NO: 162, SEQ ID NO: 173, SEQ ID NO: 176, SEQ ID NO: 187, SEQ ID NO: 190, SEQ ID NO: 201, SEQ ID NO: 204, SEQ ID NO: 215, SEQ ID NO: 218, SEQ ID NO: 229, SEQ ID NO: 232, SEQ ID NO: 243, SEQ ID NO: 246, SEQ ID NO: 257, or SEQ ID NO: 260, SEQ ID NO: 271, or SEQ ID NO: 274, or polypeptide constructs that bind to CLDN6.

[0037] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of an amino acid sequence selected from the group shown below. - Sequence IDs 19, 20, 21, 22, 23, and 24, - Sequence IDs 33, 34, 35, 36, 37, and 38, - Sequence IDs 47, 48, 49, 50, 51 and 52, - Sequence IDs 61, 62, 63, 64, 65 and 66, - Sequence IDs 75, 76, 77, 78, 79 and 80, - Sequence IDs 89, 90, 91, 92, 93 and 94, - SEQ ID NOs: 103, 104, 105, 106, 107 and 108, - Sequence IDs 117, 118, 119, 120, 121 and 122, - Sequence IDs 131, 132, 133, 134, 135 and 136, - Sequence IDs 145, 146, 147, 148, 149 and 150, - Sequence IDs 159, 160, 161, 162, 163, and 164, - Sequence IDs 173, 174, 175, 176, 177 and 178, - Sequence IDs 187, 188, 189, 190, 191 and 192, - Sequence IDs 201, 202, 203, 204, 205, and 206, - Sequence IDs 215, 216, 217, 218, 219, and 220, - Sequence IDs 229, 230, 231, 232, 233 and 234, - Sequence IDs 243, 244, 245, 246, 247 and 248, - Sequence IDs 257, 258, 259, 260, 261 and 262, and - Polypeptide constructs that compete with binding to SEQ ID NOs. 271, 272, 273, 274, 275, and 276, or CLDN6.

[0038] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 21.

[0039] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 24.

[0040] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 35.

[0041] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 38.

[0042] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 49.

[0043] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 52.

[0044] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 63.

[0045] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 66.

[0046] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 77.

[0047] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 80.

[0048] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 234.

[0049] The present invention relates to a polypeptide / polypeptide construct according to any one of the preceding paragraphs, comprising or consisting of the amino acids shown in Sequence ID No. 276.

[0050] A polypeptide / polypeptide construct according to any one of the preceding embodiments, which induces at least 100-fold, at least 250-fold, at least 500-fold lower cytotoxicity, or at least 1000-fold lower T cell-dependent cytotoxicity, as determined by an in vitro assay using cells expressing a variant of wild-type CLDN6 as shown in SEQ ID NO: 1, comprising at least one or more of the following mutations: M29X (where X is preferably L), R145X (where X is preferably Q), and / or Q156X (where X is preferably L), compared to T cell-dependent cytotoxicity measured by an in vitro assay using cells expressing CLDN6 as shown in SEQ ID NO: 1.

[0051] According to the present invention, polypeptides / polypeptide constructs are provided, in which, - The domain of the polypeptide construct of the present invention (including a paratope, i.e., an antigen-binding (epitope-binding) structure) can bind to and distinguish between CLDN6 on the surface of a cell expressing CLDN6 as shown in SEQ ID NO: 1 and the CLDN6 mutant on the surface of a cell expressing the CLDN6 mutant, wherein the CLDN6 mutant is the sequence shown in SEQ ID NO: 1, in which at least one of residues 31, 38, and 39 is substituted with another amino acid residue, in particular residue 31 being R and / or residue 38 being S and / or residue 39 being N and / or at least one of residues 31, 38, and 39 being substituted with another amino acid residue, in particular residue 156 being not Q, - Depending on the circumstances, the domain of the polypeptide construct of the present invention (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) may bind to CD3 (particularly human or non-human primate CD3), - If the (paratope (i.e., antigen-binding (epitope-binding) structure)) binds to CLDN6 on the surface of a cell expressing CLDN6, and if the further antigen-binding (epitope-binding) domain includes a paratope that binds to CD3, then the polypeptide / polypeptide construct can engage with T cells, activate T cells, and induce T cell-dependent cell-mediated cytotoxicity. - Here, the domain that binds to CLDN6 (having a paratope (i.e., an antigen-binding (epitope-binding) structure) includes a heavy chain CDR3 region containing the sequence:X1LIVX2APX3 (SEQ ID NO: 667), where X1 is either A or N, X2 is either V or E, and X3 is either V or A. - In some cases, the polypeptide construct may not selectively bind to CLDN1, CLDN2, CLDN3, CLDN4, CLDN9, and / or CLDN18.1. Preferably, the polypeptide / polypeptide construct is bound to the E1A and / or E2B regions of CLDN6 (SEQ ID NO: 1), as shown in SEQ ID NOs: 9 and 10. Preferably, the polypeptide / polypeptide construct does not bind to the epitope containing amino acids 138-150 of CLDN6 (SEQ ID NO: 1).

[0052] According to the present invention, polypeptides / polypeptide constructs are provided, in which, - The domain of the polypeptide construct of the present invention (including a paratope, i.e., an antigen-binding (epitope-binding) structure) can bind to and distinguish between CLDN6 on the surface of a cell expressing CLDN6 as shown in SEQ ID NO: 1 and a CLDN6 variant on the surface of a cell expressing the CLDN6 variant, wherein the CLDN6 variant is the sequence shown in SEQ ID NO: 1, and at least one of residues 31, 38, and 39 is substituted with another amino acid residue, in particular residue 31 being R and / or residue 38 being S and / or residue 39 being N. In some cases, the domain of the construct of the present invention (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) may bind to CD3 (particularly human or non-human primate CD3), Furthermore, if (for example, a paratope (i.e., an antigen-binding (epitope-binding) structure)) binds to CLDN6 on the surface of a cell expressing CLDN6, and if an additional antigen-binding (epitope-binding) domain includes a paratope that binds to CD3, the polypeptide / polypeptide construct can engage with T cells, activate T cells, and induce T cell-dependent cell-mediated cytotoxicity. Here, the domain that binds to CLDN6 (having a paratope (i.e., an antigen-binding (epitope-binding) structure) includes a heavy chain CDR3 region containing the sequence:DX1LIVX2APX3T (SEQ ID NO: 668), where X1 is either A or N, X2 is either V or E, and X3 is either V or A. In some cases, the domains (which have paratopes (i.e., antigen-binding (epitope-binding) structures)) do not bind immunospecifically or immunoselectively to CLDN1, CLDN2, CLDN3, CLDN4, CLDN9 and / or CLDN18.1. In some cases, the domain of the polypeptide construct of the present invention (which comprises a paratope (i.e., an antigen-binding (epitope-binding) structure)) can bind to CLDN6 on the surface of a cell expressing CLDN6 and identify CLDN6 that binds to the E1A and / or E2B regions of CLDN6 (SEQ ID NO: 1).

[0053] According to the present invention, polypeptides / polypeptide constructs are provided, in which, A polypeptide / polypeptide construct (a domain comprising a paratope (i.e., an antigen-binding (epitope-binding) structure)) capable of binding to and identifying CLDN6 on the surface of cells expressing the CLDN6 shown in SEQ ID NO: 1 and the CLDN6 variant on the surface of cells expressing the CLDN6 variant, wherein the CLDN6 variant includes the sequence shown in SEQ ID NO: 1, and at least one of residues 31, 38, and 39 is substituted with another amino acid residue, in particular residue 31 being R and / or residue 38 being S and / or residue 39 being N. In some cases, the domain of the construct of the present invention (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) may bind to CD3 (particularly human or non-human primate CD3), Furthermore, if (for example, a paratope (i.e., an antigen-binding (epitope-binding) structure)) binds to CLDN6 on the surface of a cell expressing CLDN6, and if an additional antigen-binding (epitope-binding) domain includes a paratope that binds to CD3, the polypeptide / polypeptide construct can engage with T cells, activate T cells, and induce T cell-dependent cell-mediated cytotoxicity. Here, the domain that binds to CLDN6 (having a paratope (i.e., an antigen-binding (epitope-binding) structure) includes a heavy chain CDR3 region containing the sequence: DX1LIVX2APX3TRDYYYYGMDV (SEQ ID NO: 669), where X1 is either A or N, X2 is either V or E, and X3 is either V or A. In some cases, the domain that binds to CLDN6 (which has a paratope (i.e., an antigen-binding (epitope-binding) structure)) does not bind (immunoselectively or immunoselectively) to CLDN1, CLDN2, CLDN3, CLDN4, CLDN9, CLDN18.1 and / or CLDN18.2. In some cases, the domain of the polypeptide construct of the present invention (which comprises a paratope (i.e., an antigen-binding (epitope-binding) structure)) can bind to CLDN6 on the surface of a cell expressing CLDN6 and identify CLDN6 that binds to the E1A and / or E2B regions of CLDN6 (SEQ ID NO: 1). In embodiments, the polypeptide / polypeptide construct can bind to CLDN6 on the surface of a cell expressing CLDN6, binds to the E1A and / or E2B regions of CLDN6 (SEQ ID NO: 1), and does not bind to amino acids 138-150 of CLDN6 as shown in SEQ ID NO: 1.

[0054] According to the present invention, polypeptides / polypeptide constructs are provided, in which, - A polypeptide / polypeptide construct (having a paratope (i.e., an antigen-binding (epitope-binding) structure) domain capable of binding to and identifying CLDN6 on the surface of cells expressing the CLDN6 shown in SEQ ID NO: 1 and the CLDN6 variant on the surface of cells expressing the CLDN6 variant, wherein the CLDN6 variant includes the sequence shown in SEQ ID NO: 1, and at least one of residues 31, 38, and 39 is substituted with another amino acid residue, in particular residue 31 being R and / or residue 38 being S and / or residue 39 being N, - Depending on the circumstances, the domain of the construct of the present invention (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) may bind to CD3 (particularly human or non-human primate CD3), - Furthermore, if the polypeptide / polypeptide construct binds to CLDN6 on the surface of a cell expressing CLDN6 (for example, through a paratope (i.e., an antigen-binding (epitope-binding) structure)), and if the additional antigen-binding (epitope-binding) domain includes a paratope that binds to CD3, then the polypeptide / polypeptide construct can engage with T cells, activate T cells, and induce T cell-dependent cell-mediated cytotoxicity. - A domain (with a paratope (i.e., an antigen-binding (epitope-binding) structure) capable of binding to and recognizing CLDN6 on the surface of a cell expressing CLDN6 as shown in SEQ ID NO: 1 comprises a heavy chain fragment containing a heavy chain CDR3 region containing a sequence selected from the group of sequences shown in any one of SEQ ID NOs: 15, 23, 31, 39, 47, 55, 63, 71, 79, 87, 95, 103, 111, 119, 127, 135, 143, and 151, particularly from the group containing the sequences shown in SEQ ID NOs: 15, 23, 31, and 47, and more specifically, the heavy chain CDR3 region contains or consists of SEQ ID NO: 15. - In some cases, the polypeptide construct may not selectively bind to CLDN2 (SEQ ID NO: 5), CLDN3 (SEQ ID NO: 6), CLDN4 (SEQ ID NO: 7), CLDN9 (SEQ ID NO: 8), CLDN18.1 (SEQ ID NO: 2), and / or CLDN18.2 (SEQ ID NO: 3), and / or - The construct binds to the E1A and / or E2B regions of CLDN6 (SEQ ID NO: 1), but does not bind to amino acids 138-150 of CLDN6 as shown in SEQ ID NO: 1.

[0055] The present invention provides a polypeptide / polypeptide construct comprising a domain that binds to human CLDN6 (SEQ ID NO: 1), a domain that binds to human CD3, and a domain that extends the half-life of the polypeptide as defined throughout the specification and claims, wherein the domain that binds to CLDN6 comprises a CDR1 region shown in the following sequence RASQSVX1SX2YLA (SEQ ID NO: 695) (X1 is selected from S and R, preferably S, and X2 is selected from S and T, preferably S), and / or a CDR3 region shown in the following sequence QQYX1X2SPX3T (SEQ ID NO: 696) (X1 is selected from G, D, and Q, preferably G, X2 is selected from S, A, and T, preferably S, and X3 is selected from L and I, preferably L). In one particular embodiment, the polypeptide / polypeptide construct comprises a VL chain containing the CDR1 region shown in SEQ ID NO: 16 and the CDR3 region shown in SEQ ID NO: 18, more preferably the VL CDR2 region shown in SEQ ID NO: 17, in combination with the CDR1, CDR2, and CDR3 regions of a variable heavy (VH) chain domain shown in SEQ ID NOs: 13, 14, and / or 15, and these polypeptides / polypeptides bind to the CLDN6 region shown in SEQ ID NOs: 9 and / or 10, as determined by domain swap experiments (see the Examples section). The polypeptides or polypeptide constructs of the present invention are particularly well suited to distinguishing CLDN6 from CLDN9 and have been found to bind to CLDN6 cells, e.g., CHO cells transformed with nucleic acids encoding either CLDN6 or CLDN9, and effectively kill CLDN6 cells in vitro. Not only is the cytotoxic activity better, but the polypeptides or polypeptide constructs also exhibit remarkably high protein stability, as determined by DLS°C agglutination thermal stability tests at 1 mg / ml, when they have the above-mentioned CDRs. These characteristics are important in immuno-oncology (T-cell-involved) therapeutic methods, as well as in polypeptides and / or polypeptides used for the preparation and storage of pharmaceutical formulations.

[0056] According to the present invention, a polypeptide / polypeptide construct is provided in which the domain (having a paratope (i.e., an antigen-binding (epitope-binding) structure)) binds to CLDN6 as defined in any one of the above sections and further comprises a domain (having a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CD3, particularly to a CD3-binding paratope such as disclosed in, for example, International Publication No. 2019 / 133961, exhibiting cross-species specificity only to human and macaque, or to Callitrix jaccus, Saginus oedipus, or Cymiri siurus CD3ε chains, but does not demonstrate T cell nonspecific activation to the same extent as observed with previous generations of T cell-engaging antibodies in recognizing this specific epitope (instead of the previously described epitopes of CD3 conjugates in bispecific T cell-engaging molecules). Sequences of CD3-binding domains / paratopes that can be used in association with the antibodies and constructs of the present invention are described below in their respective paragraphs.

[0057] Advantageously, targeting the CLDN6 epitope recognized by the construct of the present invention (see also the Examples section) yields the following advantages: (1) Immunospecificity / immunoselectivity of CLDN6xCD3 constructs against CLDN9 (Examples 1 and 5), and (2) Unexpectedly high cytotoxic efficacy against CLDN6xCD3 constructs (Examples 4, 6, 7, and 7).

[0058] According to the present invention, the polypeptide / polypeptide construct of the present invention includes an antigen-binding (epitope-binding) domain (having a paratope (i.e., an antigen-binding (epitope-binding) structure) that specifically and selectively binds to CD3 normally expressed on T cells.

[0059] Examples of CD3ε extracellular domains bound by this domain / paratope are shown in SEQ ID NOs: 442 and 443, respectively. Furthermore, examples of CD3ε-binding domain / paratope amino acids, and the scFv, VH chain, and VL chain containing them are shown in SEQ ID NOs: 444 to 562, and especially SEQ ID NOs: 670 to 678.

[0060] The present invention also provides a binding domain that binds to an extracellular epitope of a human CD3ε chain, which includes or consists of a VH region linked to a VL region. - i) The VH region is, • CDR-H1 sequence of X1YAX2N (wherein X1 is K, V, S, G, R, T, or I, and X2 is M or I); · The CDR-H2 sequence of RIRSKYNNYATYYADX1VK X2 (wherein X1 is S or Q, and X2 is D, G, K, S or E); and ·CDR-H3 array of HX1NFGNSYX2SX3X4AY (wherein X1 is G, R or A, X2 is I, L, V or T, X3 is Y, W or F, and X4 is W, F or Y); and - ii) The VL region is, ·CDR-L1 sequence X1SSTGAVTX2X3X4YX5N (wherein X1 is G, R, or A, X2 is S or T, X3 is G or S, X4 is N or Y, and X5 is P or A); ·CDR-L2 array of X1TX2X3X4X5X6; (wherein X1 is G or A, X2 is K, D or N, X3 is F, M or K, X4 is L or R, X5 is A, P or V, and X6 is P or S); and ·CDR-L3 sequence of X1LWYSNX2WV (wherein X1 is V, A or T, and X2 is R or L); and - iii)i) and / or ii) the CDR sequence is X24V or X24F in CDR-H1; • D15 (preferably E), X116A in CDR-H2; ·H1 (preferably A or N), X12E, F4 (preferably I) and / or N6 (preferably S or T) in CDR-H3; and • Consists of one or more amino acid substitutions selected from W93 (preferably Y) of CDR-L3.

[0061] The present invention relates to compounds that may have linkers, half-life-extending peptides, and other structural moieties, as disclosed in SEQ ID NOs. 563-575 and SEQ ID NOs. 576-666, respectively. Details regarding the function of these structures can be found in the sequence listing following the Examples section.

[0062] The polypeptide / polypeptide construct according to the present invention is assumed to include a domain (including a paratope) that binds to CD3 on the surface of a T cell, and comprises a VL region selected from the group consisting of VL regions shown in sequence listings, particularly sequence numbers 507-512, and sequence numbers 444-562 and 677, respectively, as exemplified by sequence numbers 534-541 and 677.

[0063] In another embodiment, the polypeptide / polypeptide construct according to the present invention comprises a domain (including a paratope) that binds to CD3 on the surface of a T cell, which includes the VL region shown in SEQ ID NO: 677.

[0064] The polypeptide / polypeptide construct according to the present invention may also include a domain (including a paratope) that binds to CD3 on the surface of a T cell, which is a VH region selected from the group consisting of VH regions shown in sequence lists, particularly sequence numbers 444-562 and 676, as exemplified by sequence numbers 513-533 and 676.

[0065] In another embodiment, the polypeptide / polypeptide construct according to the present invention comprises a domain (including a paratope) that binds to CD3 on the surface of a T cell, which includes the VH region shown in Sequence ID No. 676.

[0066] More preferably, the polypeptide / polypeptide construct according to the present invention, which includes a domain (including a paratope) that binds to CD3 on the surface of a T cell, includes a pair of VL and VH regions selected from the group consisting of VL and VH regions shown in each of the sequence numbers exemplified in the sequence listing, particularly the following pairs of VL and VH regions, particularly SEQ ID NOs: 507+514, 508+519, 509+521, 510+525, 511+528, 512+532, 534+513, 535+515, 536+516, 537+517, 538+518, 539+520, 540+522, and 541+523, and more specifically the pair of VL and VH regions shown in SEQ ID NO: 676+677.

[0067] A preferred embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, comprising an amino acid sequence selected from the group consisting of SEQ ID NOs. 542-562 and SEQ ID NO. 678.

[0068] A particular embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, comprising the amino acid sequence shown in SEQ ID NO: 678.

[0069] A particular embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, comprising the amino acid sequence shown in SEQ ID NO: 678, and a domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6, SEQ ID NO: 678 CLDN6 is composed of, or competes with, a CLDN6 having pairs of VH and VL regions containing the amino acid sequences shown in 11+12, SEQ ID NOs: 25+26, 39+40, 53+54, 67+68, 81+82, 95+96, 109+110, 123+124, 137+138, 151+152, 165+166, 179+180, 193+194, 207+208, 221+222, 235+236, 249+250, or 263+264.

[0070] A particular embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, comprising the amino acid sequence shown in SEQ ID NO: 678, and a domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure) that binds to CLDN6, as shown in SEQ ID NO: 19, SEQ ID NO: 22, SEQ ID NO: 33, SEQ ID NO: 36, SEQ ID NO: 47, SEQ ID NO: 50, SEQ ID NO: 61, SEQ ID NO: 64, SEQ ID NO: 75, SEQ ID NO: 78, SEQ ID NO: 89, SEQ ID NO: 92, SEQ ID NO: 103, SEQ ID NO: 1 CLDN6 is composed of or competes with 06, 117, 120, 131, 134, 145, 148, 159, 162, 173, 176, 187, 190, 201, 204, 215, 218, 229, 232, 243, 246, 257, or 260, 271, or 274, which contain the amino acid sequence shown in 06, 117, 120, 131, 134, 145, 148, 159, 162, 173, 176, 187, 190, 201, 204, 215, 218, 229, 232, 243, 246, 257, or 260, 271, or 274.

[0071] A particular embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, comprising the amino acid sequence shown in SEQ ID NO: 678, and a domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6 is represented by SEQ ID NOs selected from the group including SEQ ID NOs: 19, 22, 33, 36, 47, 50, 75, 78, 201 and 204, particularly SEQ ID NOs: 19 and 22, and very particularly SEQ ID NO: 22.

[0072] Other specific embodiments of the polypeptide / polypeptide construct according to the present invention feature a domain (including a paratope) that binds to CD3 on the surface of a T cell, comprising the amino acid sequence shown in SEQ ID NO: 678, and a domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6, as shown in SEQ ID NO: 22.

[0073] A very specific embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, the domain comprising the VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in SEQ ID NOs. 670, 671, and / or 672, and / or the domain (including a paratope) that binds to CD3 on the surface of a T cell comprises the VL CDR sequences LCDR1, LCDR2, and / or LCDR3 shown in SEQ ID NOs. 673, 674, and / or 675, and the domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6 is represented by any one of the sequences shown in SEQ ID NOs. 22, 36, 50, 78, and 204.

[0074] Another very specific embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, the domain comprising the VH CDR sequences HCDR1, HCDR2 and / or HCDR3 shown in SEQ ID NOs. 670, 671 and / or 672, and / or the domain comprising the VL CDR sequences LCDR1, LCDR2 and / or LCDR3 shown in SEQ ID NOs. 673, 674 and / or 675, the domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6 comprising the VH CDR sequences HCDR1, HCDR2 and / or HCDR3 as shown in SEQ ID NOs. 13, 14 and / or 15, and / or the (paratope-containing) domain comprising LCDR1, LCDR2 and / or LCDR3 shown in any one of the sequences shown in SEQ ID NOs. 16, 17 and / or 18.

[0075] A further very specific embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, wherein the domain comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 670, 671, and / or 672, and / or the domain comprises VL CDR sequences LCDR1, LCDR2, and / or LCDR3 shown in any one of the sequences shown in SEQ ID NOs. 673, 674, and / or 675, and the domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6 comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 27, 28, and / or 29, and / or the (paratope-containing) domain comprises VL The CDR sequence includes LCDR1, LCDR2, and / or LCDR3.

[0076] A further very specific embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, wherein the domain comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 670, 671, and / or 672, and / or the domain comprises VL CDR sequences LCDR1, LCDR2, and / or LCDR3 shown in any one of the sequences shown in SEQ ID NOs. 673, 674, and / or 675, and the domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6 comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 41, 42, and / or 42, and / or the (paratope-containing) domain comprises VL The CDR sequence includes LCDR1, LCDR2, and / or LCDR3.

[0077] A further very specific embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, wherein the domain comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 670, 671, and / or 672, and / or the domain comprises VL CDR sequences LCDR1, LCDR2, and / or LCDR3 shown in any one of the sequences shown in SEQ ID NOs. 673, 674, and / or 675, and the domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6 comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 69, 70, and / or 71, and / or the (paratope-containing) domain comprises VL The CDR sequence includes LCDR1, LCDR2, and / or LCDR3.

[0078] A further very specific embodiment of the polypeptide / polypeptide construct according to the present invention is characterized by a domain (including a paratope) that binds to CD3 on the surface of a T cell, wherein the domain comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 670, 671, and / or 672, and / or the domain comprises VL CDR sequences LCDR1, LCDR2, and / or LCDR3 shown in any one of the sequences shown in SEQ ID NOs. 673, 674, and / or 675, and the domain (including a paratope (i.e., an antigen-binding (epitope-binding) structure)) that binds to CLDN6 comprises VH CDR sequences HCDR1, HCDR2, and / or HCDR3 shown in any one of the sequences shown in SEQ ID NOs. 195, 196, and / or 197, and / or the (paratope-containing) domain comprises VL The CDR sequence includes LCDR1, LCDR2, and / or LCDR3.

[0079] Method for producing nucleic acids, host cells, and compounds of the present invention In a second aspect, it is further assumed that, in the context of the present invention, a polynucleotide encoding a polypeptide construct of the present invention as shown in any one of the preceding sections is provided.

[0080] In connection with the present invention, it is also conceivable to provide a vector containing the polynucleotide of the present invention.

[0081] Furthermore, the present invention provides host cells transformed or transfected with polynucleotides or the vector of the present invention.

[0082] In connection with the present invention, it is also conceivable to provide a method for producing a polypeptide construct of the present invention, comprising culturing host cells of the present invention under conditions that enable the expression of the construct, and recovering the polypeptide construct produced from the culture.

[0083] Pharmaceutical composition of the present invention In a further embodiment, the present invention provides a pharmaceutical composition comprising a polypeptide compound of the present invention or a polypeptide compound produced according to the method of the present invention.

[0084] In some embodiments, the pharmaceutical composition may also be assumed to be stable at approximately -20°C for at least four weeks.

[0085] Therapeutic use / method of the present invention In connection with the present invention, it is further envisioned to provide polypeptide compounds and pharmaceutical compositions of the present invention, or polypeptide compounds and pharmaceutical compositions comprising such polypeptide compounds produced according to the method of the present invention, for use as pharmaceuticals, particularly for use in the prevention, treatment, or improvement of diseases selected from proliferative disorders, neoplastic disorders, cancer, or immunodeficiencies.

[0086] In connection with the present invention, it is further envisioned that a method for treating or improving proliferative disorders, neoplastic disorders, cancer, or immunological disorders is provided, comprising the step of administering a polypeptide compound or pharmaceutical composition of the present invention to a subject in need thereof, wherein the compound is optionally produced in accordance with the method of the present invention.

[0087] Preferably, the diseases include bladder cancer, ovarian cancer, particularly ovarian adenocarcinoma and ovarian teratocarcinoma, lung cancer including small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), particularly squamous cell lung cancer and adenocarcinoma, gastric cancer, breast cancer, liver cancer, pancreatic cancer, skin cancer, particularly basal cell carcinoma and squamous cell carcinoma, malignant melanoma, head and neck cancer, particularly malignant pleomorphic adenoma, sarcoma, particularly synovial sarcoma and carcinosarcoma, bile duct cancer, bladder cancer, particularly transitional cell carcinoma and papillary carcinoma, kidney cancer, particularly renal cell carcinoma including clear cell renal cell carcinoma and papillary renal cell carcinoma, colon cancer, ileum cancer, particularly small intestinal cancer including small intestinal adenocarcinoma and ileal adenocarcinoma, embryonal testicular cancer, placental choriocarcinoma, cervical cancer, testicular cancer, particularly testicular seminoma, testicular teratoma and embryonic testicular cancer The group includes various types of cancers expressing CLDN6, selected from the group consisting of uterine cancer, germ cell tumors such as teratoma or embryonic carcinoma, particularly germ cell tumors of the testes, and their metastatic forms, very particularly testicular germ cell carcinoma, uterine cancer such as ovarian cancer, particularly ovarian serous cystadenocarcinoma, and endometrial cancer of the uterine body, lung cancer including small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), such as lung adenocarcinoma, triple-negative breast cancer, gastric cancer, bile duct cancer, esophageal cancer, Wilms' tumor, rhabdoid tumor, particularly ovarian cancer, uterine cancer, and / or lung cancer, more specifically ovarian serous cystadenocarcinoma, uterine cancer, endometrial cancer of the uterine body, and / or particularly lung squamous cell carcinoma and lung adenocarcinoma.

[0088] The use of the compounds described herein for preparing pharmaceuticals for the treatment, prevention, or improvement of neoplastic diseases, particularly ovarian cancer, uterine cancer, and / or lung cancer is also provided.

[0089] In connection with the present invention, it is envisioned that a method for treating or improving gastrointestinal cancer will be provided, comprising the step of administering constructs for CLDN6 and CD3 to a subject in need thereof.

[0090] In connection with the present invention, it is also conceivable to provide polypeptide / polypeptide constructs for CLDN6 and CD3 for use as pharmaceuticals, particularly for use in the treatment or improvement of ovarian cancer, uterine cancer, lung cancer, particularly ovarian cancer, particularly ovarian adenocarcinoma and ovarian teratocarcinoma, lung cancer (including small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC)), particularly squamous cell lung cancer and adenocarcinoma.

[0091] The present invention kit In another embodiment, within the context of the present invention, it is also conceivable to provide a kit comprising the polypeptide construct of the present invention, or a polypeptide construct prepared according to the method of the present invention, the polynucleotide of the present invention, the vector of the present invention, and / or the host cell of the present invention.

[0092] Definitions of terms according to the present invention The term “polypeptide construct” (or simply “compound”) refers to an antigen-binding (or epitope-binding) molecule that includes the paratope-containing domain itself. In the context of the present invention, a polypeptide construct is understood as an organic polymer containing at least one contiguous, unbranched amino acid chain that is not naturally occurring but has been manipulated. An example of a polypeptide construct that is a single polypeptide is the BiTE® molecule, which contains a core structure on a single polypeptide chain containing at least one functional target-binding domain and at least one fully functional CD3-binding domain, where these domains are directly linked by a flexible peptide ("linker") without further insertion domains, unlike Xmab, which contains target-binding and CD3-binding agents on different polypeptide chains. In connection with the present invention, similar polypeptide constructs containing multiple amino acid chains are also envisioned. While the term “polypeptide” is preferably used in relation to the single-chain form of the compounds of the present invention, “polypeptide construct” may be more appropriately used to describe polypeptides containing two or more polypeptide chains, e.g., two, three, or four polypeptide chains. Furthermore, the term “polypeptide construct” is also suitable for describing the compounds of the present invention that include one or more non-amino acid components, such as human serum albumin (HSA). The amino acid chain of the polypeptide typically contains at least 50 amino acids, preferably at least 100, 200, 300, 400, or 500 amino acids. Also in connection with the present invention, it is conceivable that the amino acid chain of the polymer may be linked to entities that are not composed of amino acids.

[0093] Polypeptides include structural and / or functional features based on the structure and / or function of antibodies, such as full-length immunoglobulin molecules. Therefore, polypeptide constructs bind specifically, preferably selectively or immunospecifically, to their target or antigen, more precisely, to the epitope of the target or target antigen, and / or include domains containing or derived from naturally occurring heavy chain variable regions (VH) and / or light chain variable regions (VL) in antibodies. Thus, constructs may, in alternative terms, be considered to include paratope-structuring structures (i.e., the formation of a paratope structure) and epitope-binding structures, such as structures found in natural antibodies or fragments thereof. The polypeptide constructs according to the present invention include the minimum structural requirements of an antibody that enables immunospecific target binding, i.e., a paratope that immunospecifically or immunoselectively recognizes an epitope on a target antigen. This minimum requirement can be defined, for example, by the presence of at least three light chain CDRs (i.e., CDR1, CDR2, and CDR3 in the VL region) and / or three heavy chain CDRs (i.e., CDR1, CDR2, and CDR3 in the VH region), preferably all six CDRs. Thus, polypeptide constructs can be characterized by the presence of three or six CDRs in either one or both binding domains, and those skilled in the art will know where (in what order) those CDRs are located within the paratope-binding structure. As used herein, the term “antigen-binding structure” refers to any polypeptide comprising an antigen-binding structure or any molecule having binding activity to an antigen. Peptides and proteins are not limited to those of biological origin, but may also be polypeptides produced from, for example, artificially designed sequences. They may also be naturally occurring polypeptides, synthetic polypeptides, recombinant polypeptides, etc. Since the antigen-binding structures of the present invention bind specifically to a portion of an antigen, i.e., specifically to an epitope, the antigen (epitope)-binding structures may also be defined as “paratope structures.”Accordingly, the polypeptide / polypeptide construct according to the present invention may also be defined as a domain comprising a paratope that preferably binds immunospecifically or immunoselectively to a target antigen / target epitope, and a further paratope domain that preferably binds immunospecifically or immunoselectively to a further target antigen / target epitope of the CD3 molecule as defined herein. Accordingly, whenever this specification refers to a domain of a compound or molecule of the present invention, the construct comprises at least one paratope structure (or paratope) that binds to CLDN6 as defined herein, in particular by any one of the appended claims, and a further paratope structure that binds to CD3 as defined herein.

[0094] As used in this invention, the term “antibody” includes full-length antibodies, including camel antibodies and other immunoglobulins produced by biotechnological or protein engineering methods or processes. These full-length antibodies may be, for example, monoclonal antibodies, recombinant antibodies, chimeric antibodies, deimmunized antibodies, humanized antibodies and human antibodies, as well as antibodies from other species such as mice, hamsters, rabbits, rats, goats or non-human primates.

[0095] The polypeptide / polypeptide constructs of the present invention may also include the structure of full-length immunoglobulins as they exist in nature. For example, an antibody construct may include (at least) two full-length antibody heavy chains and two full-length antibody light chains. However, given that the polypeptide / polypeptide constructs of the present invention include one domain containing a paratope that binds to CLDN6 and another domain containing a paratope that binds to CD3, these do not exist in nature, and their functions are significantly different from those of naturally occurring products. Therefore, the polypeptides or polypeptide constructs of the present invention are artificial "hybrid" molecules containing different binding domains with different specificities and / or selectivity.

[0096] As described above, the polypeptides of the present invention may comprise two or more polypeptide chains; that is, polypeptides comprising two or more polypeptide chains are also subject to the present invention, including polypeptides that form a three-dimensional protein-like structure enabling immunospecific binding to CLDN6 and CD3 in particular. Accordingly, the definition of the term “polypeptide construct” includes molecules consisting of only one polypeptide chain and molecules consisting of two, three, four or more polypeptide chains (these chains may be identical (homodimers, homotrimers, or homooligomers) or different (heterodimers, heterotrimers, or heterooligomers)). Examples of antibodies and their fragments, variants, derivatives, and constructs derived therefrom identified above are described, in particular, in Harlow and Lane, Antibodies: A laboratory manual, CSHL Press (1988); Kontermann and Duebel, Antibody Engineering, Springer, 2nd ed. 2010; and Little, Recombinant Antibodies for Immunotherapy, Cambridge University Press 2009.

[0097] The "polypeptide / polypeptide construct" of the present invention may also include fragments of full-length antibodies such as VH, VHH, VL, (s)dAb, Fv, light chain (VL-CL), Fd(VH-CH1), heavy chain, Fab, Fab', F(ab')2, or "rIgG" (a "half-antibody" consisting of a heavy chain and a light chain). The polypeptide / polypeptide construct according to the present invention may also include modified fragments of antibodies, also called antibody variants or antibody derivatives. Examples include, but are not limited to, scFv, di-scFv or bi(s)-scFv, scFv-Fc, scFv-zipper, scFab, Fab2, Fab3, diabody, single-chain diabody, tandem diabody (Tandab's), tandem di-scFv, tandem tri-scFv, "minibody" (exemplified by structures such as (VH-VL-CH3)2, (scFv-CH3)2, ((scFv)2-CH3+CH3), ((scFv)2-CH3), or (scFv-CH3-scFv)2), multibody, e.g., triabody or tetrabody, and single-domain antibodies, e.g., nanobody or single-variable-domain antibody containing only one variable region, which may be VHH, VH, or VL, that binds selectively, preferably specifically, to an antigen or target independently of other variable regions or domains. Further possible forms of polypeptide / polypeptide constructs according to the present invention include crossovers, maximum entities, hetero-Fc constructs, mono-Fc constructs, and scFc constructs. Examples of these formats are described below herein.

[0098] Furthermore, the definition of the term "polypeptide construct" includes bivalent and polyvalent polypeptides / polypeptide constructs, as well as bispecific and polyspecific / multispecific polypeptides / polypeptide constructs that selectively and preferably specifically bind to two, three, or more antigenic structures (epitopes) via different binding domains. For example, if a polypeptide construct has two binding domains for one target (CLDN6) and one binding domain for another target (CD3), or vice versa, this antibody construct may have a binding titer greater than its specificity, in which case the polypeptide construct is trivalent and bispecific. Generally, the term "bispecificity" implies that the polypeptide construct binds to (at least) two different antigens, such as CLDN6 and CD3.

[0099] The terms “paratope,” “antigen-binding domain,” “epitope-binding domain,” “binding domain,” or “domain that binds to…” are, in relation to the present invention, characterized domains of a construct that selectively, preferably specifically, or immunospecifically bind to / interact with / recognize an epitope on a target or antigen (wherein: CLDN6 for the first domain, CD3 for the second domain). The terms “binding domain,” or “domain that binds to…” or “domain,” in relation to the “constructs” described herein, are characterized in relation to the present invention by immunospecifically binding to / interacting with / recognizing (i.e., selectively interacting with a particular amino acid) an epitope on a target or antigen. The structure and function of the first domain (binding to the target antigen) and also preferably the structure and / or function of the second domain (binding to CD3) are based on the structure and / or function of an antibody, e.g., a full-length immunoglobulin polypeptide. Therefore, “binding domain” or “domain that binds to…” may include the minimum structural requirements of an antibody that enable immunospecific target binding. The minimum structural requirement of the first domain can be defined, for example, by the presence of at least three light chain CDRs (i.e., CDR1, CDR2, and CDR3 in the VL region) and / or three heavy chain CDRs (i.e., CDR1, CDR2, and CDR3 in the VH region), preferably all six CDRs. The second domain is also assumed to include this minimum structural requirement of the antibody that enables immune-specific target binding. More preferably, the second domain also includes at least three light chain CDRs (i.e., CDR1, CDR2, and CDR3 in the VL region) and / or three heavy chain CDRs (i.e., CDR1, CDR2, and CDR3 in the VH region), preferably all six CDRs. The “~binding domain” (or “binding domain”) typically includes, but does not need to include, both the antibody light chain variable region (VL) and the antibody heavy chain variable region (VH), and may include only either VH or VL. The Fd fragment, for example, often retains the antigen-binding function of part of the intact antigen-binding domain.As used herein, the terms “paratope,” “antigen-binding structure,” and “epitope-binding structure” refer to a portion of an antibody (or a molecule according to the present invention) that contains a region that is specifically complementary to and binds to all or part of an antigen or a portion thereof, i.e., the antibody can bind only to a specific portion of the antigen. The specific portion is called an “epitope.” The antigen-binding domain can be provided from one or more antibody variable domains. Preferably, the antigen-binding domain includes an antibody variable region that includes both an antibody light chain variable region (VL) and an antibody heavy chain variable region (VH). Such preferred antigen-binding domains include, for example, “single-chain Fv(scFv),” “single-chain antibody,” “Fv,” “single-chain Fv2(scFv2),” “Fab,” and “F(ab')2.” A “paratope” may also be characterized by a specific amino acid that chemically interacts with a specific amino acid on the epitope (antigen / target) side.

[0100] Examples of formats for "binding domain," "paratope-containing domain" (or "binding domain," "antigen-binding structure," "epitope-binding structure") include full-length antibody, fragment of full-length antibody (VH, VHH, VL, etc.), (s)dAb, Fv, light chain (VL-CL), Fd(VH-CH1), heavy chain, Fab, Fab', F(ab')2 or "rIgG" ("half-antibody"), scFv, di-scFv or bi(s)-scF v, scFv-Fc, scFv-Zipper, scFab, Fab2, Fab3, Diabody, Single-chain Diabody, Tandem Diabody (Tandab's), Tandem-scFv, Tandem-scFv, Minibody, ((VH-VL-CH3)2, (scFv-CH3)2, ((scFv)2-CH3+CH3) etc. selected from minibody, ((scFv)2-CH3) or (sc Examples include, but are not limited to, single-domain antibodies such as multi-bodies (e.g., Fv-CH3-scFv)2, triabodies or tetrabodies, and nanobodies, or single variable-domain antibodies containing only one variable region which may be VHH, VH, or VL. Further examples of the format of "~binding domain" (or "binding domain") include: (1) an antibody fragment or antibody variant containing VL, VH, CL, and CH1 (e.g., Fab); (2) an antibody fragment or antibody variant containing two linked Fab fragments (e.g., F(ab')2); (3) an antibody fragment or antibody variant containing VH and CH1 (e.g., Fd); (4) an antibody fragment or antibody variant containing VL and CL (e.g., light chain); (5) an antibody fragment or antibody variant containing VL and VH (e.g., Fv); (6) a dAb fragment having a VH domain (Ward et al., (1989) Nature 341:544-546); (6) Antibody variants comprising at least three isolated CDRs of the heavy chain and / or light chain; and (7) Single-chain Fv (scFv).Examples of embodiments of the constructs or binding domains according to the present invention are described, for example, in International Publication Nos. 00 / 006605, 2005 / 040220, 2008 / 119567, 2010 / 037838, 2013 / 026837, 2013 / 026833, U.S. Patent Application Publication Nos. 2014 / 0308285, 2014 / 0302037, International Publication Nos. 2014 / 144722, 2014 / 151910, and 2015 / 048272. In relation to the present invention, a paratope is understood to be a part of the polypeptide described herein and an antigenic site that recognizes and binds to an antigen. A paratope is typically a small region of at least about five amino acids. Paratopes as understood herein typically include portions of the heavy chain (VH) and light chain (VL) sequences derived from an antibody. Each binding domain of the polypeptide according to the present invention comprises a paratope containing three sets of six complementarity-determining regions (CDR loops) contained within the antibody-derived VH and VL sequences.

[0101] With respect to compounds, particularly constructs of the present invention, it is assumed that a) the construct is a single-chain polypeptide or single-chain construct, b) the first domain is in the form of scFv, c) the second domain is in the form of scFv, d) the first and second domains are linked via a linker, preferably a peptide linker, more preferably a glycine / serine linker, and / or e) the construct contains an Fc-based domain or a domain that provides an extended serum half-life, such as human serum albumin (HSA). In the latter case, the term “polypeptide construct” is a preferred embodiment that clarifies that it contains two or more peptide chains.

[0102] The constructs of the present invention are preferably “in vitro-generated constructs” and / or “recombinant constructs.” In relation to the present invention, the term “in vitro-generated” refers to a construct according to the above definition in which all or part of the binding domain or variable region (e.g., at least one CDR) is generated by non-immune cell selection on a protein chip, e.g., in vitro phage display, or any other method that allows a candidate amino acid sequence to be tested for its ability to bind to an antigen. Thus, the term preferably excludes sequences that are generated only by genomic rearrangement in animal immune cells. The first and / or second domains of the construct are assumed to be produced or obtainable by phage display or library screening, rather than by transplanting a CDR sequence from an existing (monoclonal) antibody onto a scaffold. “Recombinant constructs” are constructs generated or fabricated using (among other) recombinant DNA technology or genetic engineering.

[0103] The constructs of the present invention are assumed to be monoclonal. As used herein, a polypeptide or construct referred to as “monoclonal” (mAb) is obtained from a substantially homogeneous population of antibodies / constructs, i.e., the individual antibodies / constructs in this population are identical (particularly with respect to their amino acid sequence) except for possible naturally occurring mutations and / or post-translational modifications (e.g., isomerization, amidation) that may be present in trace amounts. Monoclonal antibodies / constructs are highly specific, targeting a single epitope within an antigen, which contrasts with polyclonal antibody preparations, which typically contain different antibodies targeting different determinants (or epitopes). In addition to their specificity, monoclonal antibodies are advantageous in that they are synthesized by hybridoma culture and are therefore not contaminated by other immunoglobulins. The modifier “monoclonal” refers to the nature of the antibody / construct as being obtained from a substantially homogeneous population of antibodies and should not be interpreted as requiring the production of the antibody by any particular method.

[0104] Any technique that provides antibodies produced by serial cell line culture can be used to prepare monoclonal antibodies. For example, the monoclonal antibodies to be used may be produced by the hybridoma method first described by Koehler et al., Nature, 256:495 (1975), or by the recombinant DNA method (see, e.g., U.S. Patent No. 4,816,567). Further examples of techniques for producing human monoclonal antibodies include the trioma technique, the human B-cell hybridoma technique (Kozbor, Immunology Today 4 (1983), 72), and the EBV-hybridoma technique (Cole et al., Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc. (1985), 77-96).

[0105] Next, hybridomas can be screened using standard methods such as enzyme-linked immunosorbent assay (ELISA) and surface plasmon resonance (BIACORE®) analysis to identify one or more hybridomas that produce antibodies that selectively, preferably specifically or immunospecifically, bind to a particular antigen. For example, any form of relevant antigen, such as recombinant antigen, naturally occurring forms, any variant or fragment thereof, and its antigenic peptide, can be used as an immunogen. Surface plasmon resonance, as employed in the BIAcore® system, can be used to enhance the efficiency of phage antibody / construct binding to the epitope of the target antigen (Schier, Human Antibodies Hybridomas 7 (1996), 97-105; Malmborg, J. Immunol. Methods 183 (1995), 7-13).

[0106] Another exemplary method for constructing constructs or binding domains is the screening of protein expression libraries, such as phage display or ribosome display libraries. Phage display is described, for example, in Ladner et al., U.S. Patent No. 5,223,409; Smith (1985) Science 228:1315-1317; Clackson et al., Nature 352:624-628 (1991); and Marks et al., J.Mol.Biol. 222:581-597 (1991).

[0107] In addition to using display libraries, non-human animals, such as rodents (mice, hamsters, rabbits, or rats), can be immunized using relevant antigens. In one embodiment, the non-human animal contains at least a portion of a human immunoglobulin gene. For example, a large fragment of the human Ig (immunoglobulin) locus can be used to manipulate mouse strains that are deficient in mouse antibody production. Using hybridoma technology, antigen-specific monoclonal antibodies derived from genes with desired specificity can be produced and selected. See, for example, Xenomouse™, Green et al. (1994) Nature Genetics 7:13-21, U.S. Patent Application Publication No. 2003 / 0070185, International Publication Brochure No. 96 / 34096, and International Publication Brochure No. 96 / 33735.

[0108] Monoclonal antibodies, after being obtained from non-human animals, can also be modified using recombinant DNA techniques known in the art, such as humanization, deimmunization, and chimerization. Examples of modified constructs or binding domains include humanized variants of non-human antibodies / constructs, "affinity-matured" antibody constructs, or binding domains (see, e.g., Hawkins et al. J.Mol.Biol. 254, 889-896 (1992) and Lowman et al., Biochemistry 30, 10832-10837 (1991)), and antibody variants or mutants with altered effector function (see, e.g., U.S. Patent No. 5,648,260, Kontermann and Duebel (2010) and Little (2009) cited above).

[0109] In immunology, affinity maturation is the process by which B cells produce antibodies with increased affinity for an antigen during the course of an immune response. Repeated exposure to the same antigen causes the host to continuously produce antibodies with higher affinity. Similar to natural prototypes, in vitro affinity maturation is based on the principles of mutation and selection. In vitro affinity maturation has been used without issue to optimize antibodies, antibody fragments, antibody variants, constructs, or binding domains. Random mutations within the CDR are introduced using radiation, chemical mutagens, or error-prone PCR. In addition, genetic diversity can be increased by chain shuffling. Typically, two or three rounds of mutation and selection using display methods such as phage display yield antibodies, antibody fragments, antibody variants, constructs, or binding domains with affinity in the low nanomolar concentration range.

[0110] Preferred types of amino acid substitution mutations for the constructs or binding domains of the present invention involve substituting one or more residues within the hypervariable region of the parental antibody structure (e.g., a humanized antibody or human antibody structure). Generally, the resulting one or more variants selected for further development will have improved biological properties compared to the parental antibody structure from which they were generated. A simple method for producing such substitutional variants involves affinity maturation using phage display. Briefly, several sites (e.g., 6-7 sites) in the hypervariable region are mutated to generate all possible amino acid substitutions at each site. The variants thus generated are presented monovalently from filamentous phage particles as fusions with the M13 gene III product packaged within each particle. The variants presented by the phage are then screened for biological activity (e.g., binding affinity) as disclosed herein. Alanine scanning mutagenesis may also be performed to identify candidate hypervariable region sites (modification candidates) that significantly contribute to antigen binding. Alternatively, or in addition, analysis of the crystal structure of the complex between the antigen and the construct or binding domain may be useful for identifying contact sites between the binding domain and its specific antigen. Such contact residues and adjacent residues are candidates for substitution according to the techniques detailed herein. Once such variants are generated, a panel of variants may be subjected to screening as described herein, and antibodies, their antigen-binding fragments, constructs, or binding domains exhibiting superior properties in one or more relevant assays may be selected for further development.

[0111] The constructs and binding domains of the present invention particularly include “chimeric” versions in which a portion of the heavy chain and / or light chain is identical or homologous to a corresponding sequence in an antibody derived from a particular species or belonging to a particular class or subclass of antibody, and the remainder of this chain is identical or homologous to a corresponding sequence in an antibody derived from another species or belonging to another class or subclass of antibody, as well as in fragments or variants of such antibodies, to the extent that the remainder of this chain exhibits the desired biological activity (U.S. Patent No. 4,816,567; Morrison et al., Proc. Natl. Acad. Sci. USA, 81:6851-6855 (1984)). The chimeric constructs or binding domains of interest herein include “primatized” constructs that include a variable domain antigen-binding sequence derived from a non-human primate (e.g., Old World monkeys, apes, etc.) and a human constant region sequence. Various methods for producing chimeric antibodies or constructs are described. For example, see Morrison et al., Proc. Natl. Acad. ScL USA 81:6851, 1985; Takeda et al., Nature 314:452, 1985; U.S. Patent No. 4,816,567 by Cabilly et al.; U.S. Patent No. 4,816,397 by Boss et al.; European Patent No. 0171496; European Patent No. 0173494 by Tanaguchi et al.; and British Patent No. 2177096.

[0112] Antibodies, polypeptide constructs, antibody fragments, antibody variants, or binding domains can also be modified by specific deletion of human T cell epitopes (a method called "deimmunization") using methods disclosed, for example, in International Publication No. 98 / 52976 or International Publication No. 00 / 34317. In short, the heavy and light chain variable regions of antibodies, constructs, or binding domains can be analyzed with respect to MHC class II-binding peptides. These peptides correspond to potential T cell epitopes (as defined, for example, in International Publication No. 98 / 52976 and International Publication No. 00 / 34317). For the detection of potential T cell epitopes, a computer modeling technique called "peptide threading" can be applied, as described in International Publication No. 98 / 52976 and International Publication No. 00 / 34317, and in addition, motifs present in VH and VL sequences can be searched in databases of human MHC class II-binding peptides. These motifs bind to any of the 18 major MHC class I DR allotypes and thus constitute potential T cell epitopes. Detected potential T cell epitopes can be removed by substitution of a few amino acid residues within a variable domain or variable region, or preferably by single amino acid substitution. Typically, conservative substitutions are performed. In many cases, but not limited to, amino acids common to the position in human germline antibody sequences may be used. Human germline sequences are disclosed, for example, in Tomlinson, et al. (1992) J.Mol.Biol.227:776-798; Cook, GP et al. (1995) Immunol.Today Vol.16(5):237-242; and Tomlinson et al. (1995) EMBO J.14:14:4628-4638. The V BASE directory (www2.mrc-lmb.cam.ac.uk / vbase / list2.php) provides a comprehensive overview of human immunoglobulin variable region sequences (compiled by Tomlinson, LA. et al., MRC Centre for Protein Engineering, Cambridge, UK).The sequence can be used as a source of human sequences, for example, in framework regions and CDRs. For example, a consensus human framework region can also be used, as described in U.S. Patent No. 6,300,064.

[0113] Humanized antibodies, their variants or fragments, constructs, and binding domains are primarily based on human immunoglobulin sequences, which contain minimal sequences derived from non-human immunoglobulins. In most cases, humanized antibodies, their variants or fragments, constructs, and binding domains are based on human immunoglobulins (recipient antibodies), in which residues from the hypervariable region or CDR are replaced with residues from the hypervariable region or CDR of a non-human species (donor antibody), such as a rodent (e.g., mouse, hamster, rat, or rabbit), to achieve the desired specificity, affinity, ability, and / or biological activity. In some examples, Fv framework region (FR) residues of human immunoglobulins are replaced with corresponding non-human residues. Furthermore, the humanized antibodies, their variants or fragments, constructs, and binding domains used herein may also include residues not found in either the recipient or donor antibody. These modifications are made to further improve and optimize the performance of the antibody. Humanized antibodies, their variants or fragments, constructs, and binding domains may also include at least a portion of the constant region of an immunoglobulin (e.g., Fc), typically that of human immunoglobulins. For further details, see Nature, 321:522-525 (1986); Reichmann et al., Nature, 332:323-329 (1988); and Presta, Curr. Op. Struct. Biol., 2:593-596 (1992).

[0114] Humanized antibodies, their variants or fragments, constructs, and binding domains can be created by replacing the sequence of the non-antigen-binding (Fv) variable region with an equivalent sequence from the human (Fv) variable region. Exemplary methods for generating such molecules are provided in Morrison (1985) Science 229:1202-1207; Oi et al. (1986) BioTechniques 4:214; and U.S. Patents 5,585,089; 5,693,761; 5,693,762; 5,859,205; and 6,407,213. These methods involve isolating, manipulating, and expressing nucleic acid sequences encoding all or part of the immunoglobulin (Fv) variable region from at least one of the heavy or light chain. Such nucleic acids can be obtained, as described above, from hybridomas producing antibodies against a given target, as well as from other sources. Next, recombinant DNA encoding a humanized antibody, its variant or fragment, construct, or binding domain can be cloned into a suitable expression vector.

[0115] Humanized antibodies, their variants or fragments, constructs, and binding domains can also be prepared using transgenic animals (e.g., mice) that express human heavy and light chain genes but lack the ability to express endogenous mouse immunoglobulin heavy and light chain genes. Winter describes exemplary CDR grafting methods that can be used for the preparation of the humanized molecules described herein (U.S. Patent No. 5,225,539). All CDRs of a given human sequence may be replaced with at least some non-human CDRs, or only some of the CDRs may be replaced with non-human CDRs. It is sufficient to replace only the number of CDRs necessary for the humanized molecule to bind to a given antigen.

[0116] Humanized antibodies, their variants or fragments, constructs, or binding domains can be optimized by introducing conservation substitutions, consensus sequence substitutions, germline substitutions, and / or reverse mutations. Such modified immunoglobulin molecules can be prepared by any of several techniques known in the art (e.g., Teng et al., Proc. Natl. Acad. Sci. USA, 80:7308-7312, 1983; Kozbor et al., Immunology Today, 4:7279, 1983; Olsson et al., Meth. Enzymol., 92:3-16, 1982; and European Patent No. 239400).

[0117] Human anti-mouse antibody (HAMA) responses have led the industry to prepare chimeric antibodies or other humanized antibodies / constructs. However, certain human anti-chimeric antibody (HACA) reactions are expected to be observed, particularly in chronic or high-dose use of antibodies or constructs. Therefore, to alleviate concerns and / or effects of HAMA or HACA reactions, it would be desirable to provide constructs containing human-binding domains to CLDN6 and / or CD3.

[0118] Accordingly, according to one embodiment, the polypeptide construct, one binding domain and / or another binding domain is “human.” The terms “human antibody,” “human antibody construct,” and “human binding domain” include antibodies, constructs, and binding domains having antibody-derived regions such as variable regions and constant regions or domains that substantially correspond to human germline immunoglobulin sequences known in the art, including, for example, those described by Kabat et al. (1991) (cited above). The human construct or binding domain of the present invention may include, for example, amino acid residues not encoded by the human germline immunoglobulin sequence (e.g., mutations introduced in vitro by random or site-directed mutagenesis, or in vivo by somatic mutation) in, for example, the CDR, more specifically the CDR3. The human construct or binding domain may have at least one, two, three, four, five or more positions replaced by amino acid residues not encoded by the human germline immunoglobulin sequence. The definitions of human antibodies, constructs, and binding domains used herein also refer to fully human antibodies, constructs, and binding domains that consist solely of human sequences that have not been artificially and / or genetically modified, such as those that can be derived using technologies or systems such as Xenomouse.

[0119] Polypeptides / polypeptide constructs containing at least one human-binding domain avoid some of the problems associated with antibodies or constructs that have non-human variable and / or constant regions, such as those derived from rodents (e.g., mice, rats, hamsters, or rabbits). The presence of such rodent-derived proteins may lead to rapid clearance of the antibody or construct, or to an immune response by the patient to the antibody or construct. To avoid the use of rodent-derived constructs, humanized or fully human constructs can be created by introducing human antibody function into rodents so that they produce fully human antibodies.

[0120] The ability of YAC to clone and reconstruct megabase-sized human loci and to introduce them into mouse germline cells provides a powerful method for elucidating the functional elements of very large or coarsely mapped loci and for generating useful models of human diseases. Furthermore, the use of such techniques to replace mouse loci with their human equivalents can provide unique insights into the expression and regulation of human gene products during development, their communication with other systems, and their involvement in disease induction and progression.

[0121] A key practical application of such strategies is the "humanization" of the mouse humoral immune system. Introducing human immunoglobulin (Ig) loci into mice with inactivated endogenous Ig genes provides an opportunity to study the mechanisms underlying programmed antibody expression and aggregation, as well as their role in B cell development. Furthermore, such strategies can provide an ideal source for the production of fully human monoclonal antibodies (mAbs), representing a significant milestone in achieving the prospects of antibody therapy in human diseases. Fully human antibodies or constructs derived therefrom are expected to minimize the immunogenicity and allergic reactions inherent to mouse mAbs or mouse-derived mAbs, thereby increasing the efficacy and safety of the administered antibody / construct. The use of fully human antibodies or constructs is expected to yield substantial benefits in the treatment of chronic and recurrent human diseases requiring repeated administration of compounds, such as inflammation, autoimmunity, and cancer.

[0122] One approach to this goal was to manipulate mouse strains lacking mouse antibody production using large fragments of the human Ig locus, anticipating that such mice would produce a large repertoire of human antibodies in the absence of mouse antibodies. Large human Ig fragments would preserve significant variable gene diversity as well as appropriate regulation of antibody production and expression. By leveraging mouse mechanisms for antibody diversification and selection, and the lack of immune tolerance to human proteins, the reproduced human antibody repertoire in these mouse strains should produce high-affinity antibodies against any target antigen, including human antigens. Using hybridoma technology, antigen-specific human mAbs with desired specificity could be easily produced and selected. This general strategy was demonstrated in connection with the generation of the first XenoMouse mouse strain (see Green et al. Nature Genetics 7:13-21 (1994)). This XenoMouse strain was engineered using yeast artificial chromosomes (YACs) containing germline arrangement fragments of 245kb and 190kb sizes, respectively, of the human heavy chain locus and kappa light chain locus, containing core sequences of the variable and constant regions. Human Ig containing YACs proved compatible with the mouse strain for both antibody rearrangement and expression, and was able to replace the inactivated mouse Ig gene. This was demonstrated by its ability to induce B cell development, produce an adult-like human repertoire of fully human antibodies, and produce antigen-specific human mAbs. These results also suggested that the introduction of a large portion of the human Ig locus, containing numerous V genes, additional regulatory elements, and the human Ig constant region, could reproduce a substantially complete repertoire characterized by the human humoral response to infection and immunization. The study by Green et al. extended to the introduction of over 80% of the human antibody repertoire by introducing megabase-sized germline arrangement YAC fragments of the human heavy chain locus and kappa light chain locus, respectively. See Mendez et al. Nature Genetics 15:146-156 (1997) and U.S. Patent Application Publication No. 08 / 759,620.

[0123] The XenoMouse model was created using U.S. Patent Applications No. 07 / 466,008, 07 / 610,515, 07 / 919,297, 07 / 922,649, 08 / 031,801, 08 / 112,848, 08 / 234,145, 08 / 376,279, 08 / 430,938, 08 / 464,584, 08 / 464,582, 08 / 463,191, 08 / 462,837, and 08 / 4 This is discussed and detailed in Patent No. 86,853, Patent No. 08 / 486,857, Patent No. 08 / 486,859, Patent No. 08 / 462,513, Patent No. 08 / 724,752, Patent No. 08 / 759,620; and U.S. Patent No. 6,162,963, Patent No. 6,150,584, Patent No. 6,114,598, Patent No. 6,075,181 and Patent No. 5,939,598; and Japanese Patent No. 3068180B2, Japanese Patent No. 3068506B2 and Japanese Patent No. 3068507B2. See also Mendez et al. Nature Genetics 15:146-156 (1997) and Green and Jakobovits J. Exp. Med. 188:483-495 (1998), European Patent No. 0463151B1, International Publication No. 94 / 02602, International Publication No. 96 / 34096, International Publication No. 98 / 24893, International Publication No. 00 / 76310 and International Publication No. 03 / 47336.

[0124] Another approach, employed by other companies including GenPharm International, Inc., utilizes the "minilocus" approach. In the minilocus method, the exogenous Ig locus is mimicked by including fragments (individual genes) from the Ig locus. Thus, one or more VH genes, one or more DH genes, one or more JH genes, a mu constant region, and a second constant region (preferably a gamma constant region) are formed into a construct for insertion into an animal. This method is based on U.S. Patent No. 5,545,807 by Surani et al., and U.S. Patents No. 5,545,806; 5,625,825; 5,625,126; 5,633,425; 5,661,016; 5,770,429; 5,789,650; 5,814,318; and 5,877, U.S. Patent No. 397; U.S. Patent No. 5,874,299; and U.S. Patent No. 6,255,458; U.S. Patent No. 5,591,669 and U.S. Patent No. 6,023,010 by Krimpenfort and Berns; U.S. Patent No. 5,612,205; U.S. Patent No. 5,721,367; and U.S. Patent No. 5,789,215 by Berns et al.; and U.S. Patent No. 5,643,763 by Choi and Dunn; and GenPharm This is described in the U.S. Patent Applications 07 / 574,748, 07 / 575,962, 07 / 810,279, 07 / 853,408, 07 / 904,068, 07 / 990,860, 08 / 053,131, 08 / 096,762, 08 / 155,301, 08 / 161,739, 08 / 165,699, and 08 / 209,741 of International.See European Patent No. 0546073B1, International Publication No. 92 / 03918, International Publication No. 92 / 22645, International Publication No. 92 / 22647, International Publication No. 92 / 22670, International Publication No. 93 / 12227, International Publication No. 94 / 00569, International Publication No. 94 / 25585, International Publication No. 96 / 14436, International Publication No. 97 / 13852 and International Publication No. 98 / 24884, and U.S. Patent No. 5,981,175. Furthermore, see Taylor et al. (1992), Chen et al. (1993), Tuaillon et al. (1993), Choi et al. (1993), Lonberg et al. (1994), Taylor et al. (1994), Tuaillon et al. (1995), and Fishwild et al. (1996).

[0125] Kirin has also demonstrated the production of human antibodies from mice into which large chromosome fragments or entire chromosomes have been introduced by microcell fusion. See European Patent Applications Nos. 773288 and 843961. Xenerex Biosciences is developing a technology for the potential production of human antibodies. This technology involves reconstituting SCID mice with human lymphocytes, such as B and / or T cells. The mice can then be immunized with an antigen to induce an immune response to the antigen. See U.S. Patent Nos. 5,476,996; 5,698,767; and 5,958,765.

[0126] In some embodiments, the constructs of the present invention are “isolated” or “substantially pure” constructs. “Isolated” or “substantially pure,” as used in the description of constructs disclosed herein, means a construct that has been identified, separated, and / or recovered from the components of its production environment. Preferably, the construct is unrelated, or substantially unrelated, to all other components from its production environment. Contaminating components of its production environment, such as those arising from recombinant transfected cells, are materials that may interfere with the diagnostic or therapeutic use of the construct and include enzymes, hormones, and other proteinaceous or non-proteinaceous compounds. It is understood that isolated or substantially pure constructs may, depending on the context, account for 5% to 99.9% by weight of the total protein / polypeptide content in a given sample. The desired construct may be produced at significantly higher concentrations using an inducible promoter or a high-expression promoter. This definition includes the production of constructs in a wide variety of organisms and / or host cells known in the art. In certain embodiments, the construct is purified to a degree sufficient to obtain at least 15 residues of the N-terminal or internal amino acid sequence by (1) using a spinning cup sequencer, or to a degree of homogeneity by SDS-PAGE under non-reducing or reducing conditions using Coomassie blue or preferably silver staining. However, typically, the isolated construct is prepared by at least one purification step.

[0127] According to one embodiment, the entire construct and / or the binding domain is in the form of one or more polypeptides or proteins. In addition to the proteinaceous portion, such polypeptides or proteins may include non-proteinaceous portions (e.g., chemical linkers or chemical crosslinking agents, e.g., glutaraldehyde).

[0128] Peptides are short chains of amino acid monomers linked by covalent peptide (amide) bonds. Therefore, peptides are classified into a broad chemical class of biological oligomers and polymers. Amino acids that are part of a peptide or polypeptide chain are called “residues” and can be numbered sequentially. All peptides, except cyclic peptides, have an N-terminal residue at one end and a C-terminal residue at the other. Oligopeptides consist of a very small number of amino acids (usually 2 to 20). Polypeptides are longer, continuous, unbranched peptide chains. Peptides are distinguished from proteins based on size and, as an arbitrary criterion, can be understood as containing approximately 50 or fewer amino acids. Proteins typically consist of one or more polypeptides arranged in a biologically functional manner. While the aspects of the laboratory techniques used for peptides versus polypeptides and proteins (e.g., details of electrophoresis, chromatography, etc.) differ, the size boundary distinguishing peptides from polypeptides and proteins is not absolute. Therefore, in relation to this invention, the terms “peptide,” “polypeptide,” and “protein” may be used interchangeably, and the term “polypeptide” is often preferred.

[0129] As mentioned above, polypeptides can further form polymers such as dimers, trimers, and higher oligomers, which consist of two or more polypeptide molecules. The polypeptide molecules forming such dimers, trimers, etc., may be the same or different. For this reason, the corresponding structures of such higher-order polymers are referred to as homodimers or heterodimers, homotrimers or heterotrimers, etc. An example of a heteropolymer is an antibody or immunoglobulin molecule, which in its naturally occurring form consists of two identical light polypeptide chains and two identical heavy polypeptide chains. Furthermore, the terms “peptide,” “polypeptide,” and “protein” refer to naturally modified peptides / polypeptides / proteins whose modifications are achieved by post-translational modifications such as glycosylation, acetylation, and phosphorylation. Where referred to herein, “peptide,” “polypeptide,” or “protein” may be chemically modified, such as pegylation. Such modifications are well known in the art and are described below herein.

[0130] The terms “selectively,” “preferably selectively,” “(specifically or immunospecifically) bind,” “(specifically or immunospecifically) recognize,” or “(specifically or immunospecifically) react,” respectively, mean that, according to the present invention, a construct or binding domain selectively interacts with or (immunologically) specifically with a given epitope (here, CLDN6 and CD3) on a target molecule (antigen). This selective interaction or association occurs more frequently, more rapidly, for longer periods, with greater affinity, or any combination of these parameters, with respect to a specific epitope on a target (here, CLDN6) than with alternative substances (non-target molecules, e.g., CLDN4, CLDN9, CLDN3, etc.). However, due to sequence similarities between homologous proteins in various species, a construct or binding domain that selectively and / or immunospecifically binds to a target (e.g., a human target) may cross-react with homologous target molecules from different species (e.g., non-human primates). Therefore, terms such as “selective binding” and “specific / immunospecific binding” may include the binding of a construct or binding domain to two or more species of epitopes or structurally related epitopes. In relation to the present invention, the polypeptides of the present invention bind to their respective target structures in a specific manner. Preferably, the polypeptides according to the present invention contain one paratope per binding domain that “specifically or immunospecifically binds to” or “recognizes” or “reacts” with their respective target structures. This means that, according to the present invention, the polypeptide or its binding domain interacts with or (immuno)specifically with a given epitope on a target molecule (antigen) and CD3, respectively. This interaction or association occurs more frequently, more rapidly, more persistently, more favorably, or in some combination of these parameters, with respect to the epitope on a particular target compared to an alternative substance (non-target molecule). However, due to sequence similarities between homologous proteins across different species, antibody constructs or binding domains that immunospecifically bind to a target (e.g., a human target) may cross-react with homologous target molecules from different species (e.g., non-human primates).Therefore, the term “specific / immunospecific binding” may include the binding of an antibody construct or binding domain to epitopes in multiple species and / or structurally related epitopes. The term “(immuno)selectively binding” excludes binding to structurally related epitopes.

[0131] In the context of this invention, the term “epitope” refers to a portion or region of an antigen that is selectively recognized / immunospecifically by a binding structure, i.e., a paratope. Since “epitope” is antigenic, the term epitope is sometimes also referred to as “antigenic structure” or “antigenic determinant.” The portion of the binding domain that binds to the epitope is called the paratope. Specific binding is thought to be achieved by the binding domain and specific motifs in the amino acid sequence of the antigen. Thus, binding is achieved as a result of its primary structure, secondary structure, and / or tertiary structure, as well as potential secondary modifications of the structure. Specific interaction between the paratope and its antigenic determinant can cause the site to simply bind to the antigen. In some cases, instead of, or in addition to, specific interaction can induce a signal, for example, due to the induction of a change in the higher-order structure of the antigen, or the formation of an antigenic oligomer.

[0132] Epitopes of protein antigens are classified into two categories, higher-order epitopes and linear epitopes, based on their structure and interaction with paratopes. Higher-order epitopes consist of discontinuous sections of the amino acid sequence of the antigen. These epitopes interact with paratopes based on the three-dimensional surface features and shape or tertiary structure (folding) of the antigen. Methods for determining the conformation of epitopes include, but are not limited to, X-ray crystallography, two-dimensional nuclear magnetic resonance (2D-NMR) spectroscopy, and site-directed spin labeling and electron spin resonance (EPR) spectroscopy. In contrast, linear epitopes interact with paratopes based on their primary structure. Linear epitopes are formed by a continuous sequence of amino acids derived from the antigen and typically contain at least three or at least four, more commonly at least five, at least six, or at least seven, for example, about 8 to about 10 amino acids within a specific sequence.

[0133] The method for CLDN6 epitope mapping is described below. A predetermined region (a continuous amino acid stretch) within the extracellular loop of the human CLDN6 protein is replaced with the corresponding region of a CLDN6 paralog (e.g., human CLDN4 or human CLDN18.2, but other paralogs are also possible as long as the binding domain is not cross-reactive with the paralog used). These human CLDN6 / paralog chimeras are expressed on the surface of host cells (e.g., CHO cells). Antibody or construct binding can be tested via FACS analysis. If antibody or construct binding to this chimeric molecule is completely absent or significantly reduced, it can be concluded that the region of human CLDN6 removed from this chimeric molecule is associated with immunospecific epitope-paratope recognition. The reduction in binding is preferably at least 10%, 20%, 30%, 40%, or 50% compared to binding to human (wild-type) CLDN6; more preferably at least 60%, 70%, or 80% and most preferably 90%, 95%, or even 100% (where binding to human CLDN6 is 100%). Alternatively, the epitope mapping analysis described above can be modified by introducing one or more point mutations into the sequence of CLDN6, specifically the sequence of extracellular loop 1 or loop 2, more specifically the sequence corresponding to the E1A and / or E2B regions of these loops shown in SEQ ID NOs. 9 and 10. These point mutations may reflect, for example, differences between CLDN6 and its closely related paralog, CLDN4.

[0134] A further method for determining the contribution of specific residues of a target antigen to recognition by constructs or binding domains is alanine scanning (see, e.g., Morrison KL & Weiss GA. Curr Opin Chem Biol. 2001 Jun;5(3):302-7), in which each residue analyzed is replaced with alanine, for example, by site-directed mutagenesis. Alanine is used because, despite mimicking the secondary structure preference of many other amino acids, it is not bulky and has a chemically inactive methyl functional group. Sometimes, when size preservation of the mutant residue is required, bulky amino acids such as valine or leucine may be used.

[0135] The interaction between the binding domain and the epitope of the target antigen means that the binding domain exhibits a recognizable or significant affinity for the epitope / target antigen (here: CLDN6 and CD3, respectively), and generally does not exhibit a significant affinity for proteins or antigens other than the target antigen (here: CLDN6 / CD3), despite the aforementioned cross-reactivity with homologous targets from other species, or CLDN9 of the same species, particularly human CLDN6 and CLDN9. "Significant affinity" refers to binding with an affinity (dissociation constant, KD) of ≤10⁻⁶ M. Preferably, binding is considered specific when the binding affinity is ≤10⁻⁷ M, ≤10⁻⁸ M, ≤10⁻⁹ M, ≤10⁻¹⁰ M, or even ≤10⁻¹¹ M, or ≤10⁻¹² M. Whether a binding domain (immune) specifically reacts to or binds to a target can be easily tested, for example, by comparing the affinity of the binding domain to the desired target protein or antigen with the affinity of the binding domain to a non-target protein or antigen (here, proteins other than CLDN6 or CD3, respectively). Preferably, the constructs of the present invention do not significantly bind to proteins or antigens other than CLDN6 or CD3, respectively (i.e., the first domain does not bind to proteins other than CLDN6, and the second domain does not bind to proteins other than CD3) - unless any further one or more binding domains for another target are intentionally introduced into the constructs of the present invention, in which case the binding of those binding domains to their specific targets is also provided by the present invention.

[0136] The affinity of the first domain to CLDN6 (e.g., human CLDN6) is assumed to be ≤100nM, ≤90nM, ≤80nM, ≤70nM, ≤60nM, ≤50nM, ≤40nM, ≤30nM, or ≤20nM. These values ​​are preferably measured by cell-based assays such as the scatchard assay. Other affinity determination methods are also known. Furthermore, the affinity of the second domain to CD3 (e.g., human CD3) is assumed to be ≤100nM, ≤90nM, ≤80nM, ≤70nM, ≤60nM, ≤50nM, ≤40nM, ≤30nM, ≤20nM, or ≤10nM. These values ​​are preferably measured by surface plasmon resonance assays such as the Biacore assay.

[0137] The terms "not significantly binding" and "not selectively binding" mean that the construct or binding domain of the present invention does not bind to any protein or antigen other than CLDN6 or CD3 when such protein or antigen is expressed on the cell surface. Therefore, the construct exhibits reactivity with proteins or antigens other than CLDN6 or CD3 (when the protein or antigen is expressed on the cell surface) of ≤30%, preferably ≤20%, more preferably ≤10%, and particularly preferably ≤9%, ≤8%, ≤7%, ≤6%, ≤5%, ≤4%, ≤3%, ≤2%, or ≤1% (where binding to CLDN6 or CD3 is defined as 100%, respectively). "Reactivity" can be expressed, for example, by affinity values ​​(see above).

[0138] The construct of the present invention (and more specifically, the domain containing a paratope that binds to CLDN6) is expected not to bind to or significantly bind to CLDN6 paralogs, more specifically to human CLDN6 paralogs and / or macaque / cynomolgus monkey CLDN6 paralogs. It is also expected that the construct will not bind to or significantly bind to (human or macaque / cynomolgus monkey) CLDN6 paralogs on the surface of target cells. CLDN6 paralogs include, but are not limited to, CLDN1, CLDN2, CLDN3, CLDN4, CLDN18.1, CLDN18.2, and especially CLDN9. According to one embodiment, the human paralog of CLDN6 has the sequence shown in Sequence IDs 2-8. Therefore, the first domain of the construct of the present invention is expected not to bind to or significantly selectively bind to CLDN1, CLDN2, CLDN3, CLDN4, CLDN18.1, CLDN18.2, and / or CLDN9 (on the cell surface). The constructs of this invention are expected to substantially not bind to CLDN9 expressed in various organs. Selective binding to CLDN6 and essentially binding to CLDN9 avoid potential adverse events that may occur due to off-target binding.

[0139] One domain of the polypeptide construct of the present invention, comprising a paratope (antigen-binding (epitope-binding) structure), specifically and / or selectively binds to CLDN6 on the surface of a target cell. “Target cell” can be any prokaryotic or eukaryotic cell expressing CLDN6 on its surface, preferably a cell that is part of a human or animal body, such as a specific CLDN6-expressing cancer cell or tumor cell, or a CLDN6-positive neoplasm, or an artificially generated CLDN6-expressing cell (the latter, for example, may be used in an ex vivo assay). In the context of the present invention, the term “on the surface” is understood to mean that the first antigen-binding domain of the construct selectively, preferably specifically, binds to an epitope contained within a first CLDN6 extracellular loop (CLDN6 ECL1) and a second CLDN6 extracellular loop (CLDN6 ECL2), and in particular to an epitope formed by a combination of both loops. Therefore, the domain containing the paratope (antigen-binding (epitope-binding) structure) of the construct of the present invention is expected to bind to an epitope formed by one or both of the extracellular loops of CLDN6, preferably human CLDN6. The extracellular loops may be a first loop and / or a second loop. It is also particularly expected that both loops contribute to binding. In this case, one loop (e.g., the first loop) may correspond to the primary binding partner of the construct, while the other loop (e.g., the second loop) may contribute to binding, for example, as a stabilizing partner, but may not be essential for binding. Therefore, the domain containing the paratope (antigen-binding (epitope-binding) structure) according to the present invention may bind to CLDN6 when expressed by naturally expressing cells or cell lines (e.g., human cancer lines OVCAR-3, OAW28, LCLC97TM1, and NCI-H1435) and / or by cells or cell lines transformed or (stable / transiently) transfected with CLDN6. In one embodiment, the domain includes a paratope (antigen-binding (epitope-binding) structure) that binds to CLDN6 when CLDN6 is used as a target molecule in cell-based binding assays such as Scatchard.Furthermore, it is anticipated that the construct / its first domain will bind to human CLDN6 on the surface of target cells. The preferred amino acid sequence of human CLDN6 is shown in Sequence ID No. 1.

[0140] The polypeptide construct according to the present invention (more specifically, the domain containing a paratope (antigen-binding (epitope-binding) structure) that binds to CLDN6) is envisioned to bind to the first extracellular loop (ECL1, loop 1) of CLDN6. This does not necessarily preclude the second extracellular loop from also contributing to the paratope-epitope interaction site, albeit to a different degree, e.g., a lower degree. The term "CLDN6 ECL" (ECL = extracellular loop) refers to the portion of CLDN6 that does not essentially contain the transmembrane and cytoplasmic domains of CLDN6. It is understood that the transmembrane domain identified for the CLDN6-binding polypeptide of the present invention will be identified according to the criteria routinely used in the art for identifying that type of hydrophobic domain. The exact boundary of the transmembrane domain may vary, but is most likely to be about five or fewer amino acids at the end of any of the domains explicitly mentioned herein. A preferred human CLDN6 ECL1 is shown in SEQ ID NO: 9, and a preferred human CLDN6 ECL2 is shown in SEQ ID NO: 10. In a very specific embodiment, the construct according to the present invention (more specifically, the first domain of the construct) binds to CLDN6, preferably human CLDN6, which is favorably expressed on the surface of cancer cells or cells induced to express CLDN6, e.g., human CLDN6, by transformation or transfection, and does not bind to amino acids 138-150 of CLDN6, as shown in SEQ ID NO: 1.

[0141] The present invention further includes the following: a domain containing a paratope (antigen-binding (epitope-binding) structure) of the construct of the present invention preferably selectively binds to the same CLDN6 epitope as an antibody or construct containing a domain that binds to CLDN6 on the surface of a target cell. a) The VH region including CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and the VL region including CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO: 18; b) The VH region including CDR-H1 shown in SEQ ID NO: 27, CDR-H2 shown in SEQ ID NO: 28, and CDR-H3 shown in SEQ ID NO: 29, and the VL region including CDR-L1 shown in SEQ ID NO: 30, CDR-L2 shown in SEQ ID NO: 31, and CDR-L3 shown in SEQ ID NO: 32; c) The VH region including CDR-H1 shown in SEQ ID NO: 41, CDR-H2 shown in SEQ ID NO: 42, and CDR-H3 shown in SEQ ID NO: 43, and the VL region including CDR-L1 shown in SEQ ID NO: 44, CDR-L2 shown in SEQ ID NO: 45, and CDR-L3 shown in SEQ ID NO: 46; d) The VH region including CDR-H1 shown in SEQ ID NO: 55, CDR-H2 shown in SEQ ID NO: 56, and CDR-H3 shown in SEQ ID NO: 57, and the VL region including CDR-L1 shown in SEQ ID NO: 58, CDR-L2 shown in SEQ ID NO: 59, and CDR-L3 shown in SEQ ID NO: 60; e) The VH region including CDR-H1 shown in SEQ ID NO: 69, CDR-H2 shown in SEQ ID NO: 70, and CDR-H3 shown in SEQ ID NO: 71, and the VL region including CDR-L1 shown in SEQ ID NO: 72, CDR-L2 shown in SEQ ID NO: 73, and CDR-L3 shown in SEQ ID NO: 74; f) The VH region including CDR-H1 shown in SEQ ID NO: 83, CDR-H2 shown in SEQ ID NO: 84, and CDR-H3 shown in SEQ ID NO: 85, and the VL region including CDR-L1 shown in SEQ ID NO: 86, CDR-L2 shown in SEQ ID NO: 87, and CDR-L3 shown in SEQ ID NO: 88; g) The VH region including CDR-H1 shown in SEQ ID NO: 97, CDR-H2 shown in SEQ ID NO: 98, and CDR-H3 shown in SEQ ID NO: 99, and the VL region including CDR-L1 shown in SEQ ID NO: 100, CDR-L2 shown in SEQ ID NO: 101, and CDR-L3 shown in SEQ ID NO: 102; h) A VH region including CDR-H1 shown in SEQ ID NO: 111, CDR-H2 shown in SEQ ID NO: 112, and CDR-H3 shown in SEQ ID NO: 113, and a VL region including CDR-L1 shown in SEQ ID NO: 114, CDR-L2 shown in SEQ ID NO: 115, and CDR-L3 shown in SEQ ID NO: 116; i) The VH region including CDR-H1 shown in SEQ ID NO: 125, CDR-H2 shown in SEQ ID NO: 126, and CDR-H3 shown in SEQ ID NO: 127, and the VL region including CDR-L1 shown in SEQ ID NO: 128, CDR-L2 shown in SEQ ID NO: 129, and CDR-L3 shown in SEQ ID NO: 130; j) The VH region including CDR-H1 shown in SEQ ID NO: 139, CDR-H2 shown in SEQ ID NO: 140, and CDR-H3 shown in SEQ ID NO: 141, and the VL region including CDR-L1 shown in SEQ ID NO: 142, CDR-L2 shown in SEQ ID NO: 143, and CDR-L3 shown in SEQ ID NO: 144; k) The VH region including CDR-H1 shown in SEQ ID NO: 153, CDR-H2 shown in SEQ ID NO: 154, and CDR-H3 shown in SEQ ID NO: 155, and the VL region including CDR-L1 shown in SEQ ID NO: 156, CDR-L2 shown in SEQ ID NO: 157, and CDR-L3 shown in SEQ ID NO: 158; l) The VH region including CDR-H1 shown in SEQ ID NO: 167, CDR-H2 shown in SEQ ID NO: 168, and CDR-H3 shown in SEQ ID NO: 169, and the VL region including CDR-L1 shown in SEQ ID NO: 170, CDR-L2 shown in SEQ ID NO: 171, and CDR-L3 shown in SEQ ID NO: 172; m) The VH region including CDR-H1 shown in SEQ ID NO: 181, CDR-H2 shown in SEQ ID NO: 182, and CDR-H3 shown in SEQ ID NO: 183, and the VL region including CDR-L1 shown in SEQ ID NO: 184, CDR-L2 shown in SEQ ID NO: 185, and CDR-L3 shown in SEQ ID NO: 186; n) The VH region including CDR-H1 shown in SEQ ID NO: 195, CDR-H2 shown in SEQ ID NO: 196, and CDR-H3 shown in SEQ ID NO: 197, and the VL region including CDR-L1 shown in SEQ ID NO: 198, CDR-L2 shown in SEQ ID NO: 199, and CDR-L3 shown in SEQ ID NO: 200; o) The VH region including CDR-H1 shown in SEQ ID NO: 209, CDR-H2 shown in SEQ ID NO: 210, and CDR-H3 shown in SEQ ID NO: 211, and the VL region including CDR-L1 shown in SEQ ID NO: 212, CDR-L2 shown in SEQ ID NO: 213, and CDR-L3 shown in SEQ ID NO: 214; p) The VH region including CDR-H1 shown in SEQ ID NO: 223, CDR-H2 shown in SEQ ID NO: 224, and CDR-H3 shown in SEQ ID NO: 225, and the VL region including CDR-L1 shown in SEQ ID NO: 226, CDR-L2 shown in SEQ ID NO: 227, and CDR-L3 shown in SEQ ID NO: 228; q) The VH region including CDR-H1 shown in SEQ ID NO: 237, CDR-H2 shown in SEQ ID NO: 238, and CDR-H3 shown in SEQ ID NO: 239, and the VL region including CDR-L1 shown in SEQ ID NO: 240, CDR-L2 shown in SEQ ID NO: 241, and CDR-L3 shown in SEQ ID NO: 242; r) A VH region including CDR-H1 shown in SEQ ID NO: 251, CDR-H2 shown in SEQ ID NO: 252, and CDR-H3 shown in SEQ ID NO: 253, and a VL region including CDR-L1 shown in SEQ ID NO: 254, CDR-L2 shown in SEQ ID NO: 255, and CDR-L3 shown in SEQ ID NO: 256; or s) A VH region including CDR-H1 shown in SEQ ID NO: 265, CDR-H2 shown in SEQ ID NO: 266, and CDR-H3 shown in SEQ ID NO: 267, and a VL region including CDR-L1 shown in SEQ ID NO: 268, CDR-L2 shown in SEQ ID NO: 269, and CDR-L3 shown in SEQ ID NO: 270, Or a-1) The VH region shown in Sequence ID No. 11 and the VL region shown in Sequence ID No. 12; b-1) The VH region shown in Sequence ID No. 19 and the VL region shown in Sequence ID No. 20; c-1) The VH region shown in Sequence ID No. 27 and the VL region shown in Sequence ID No. 28; d-1) The VH region shown in Sequence ID No. 35 and the VL region shown in Sequence ID No. 36; e-1) The VH region shown in Sequence ID No. 43 and the VL region shown in Sequence ID No. 44; f-1) The VH region shown in Sequence ID No. 51 and the VL region shown in Sequence ID No. 52; g-1) The VH region shown in Sequence ID No. 59 and the VL region shown in Sequence ID No. 60; h-1) The VH region shown in Sequence ID No. 67 and the VL region shown in Sequence ID No. 68; i-1) The VH region shown in Sequence ID 75 and the VL region shown in Sequence ID 76; j-1) The VH region shown in Sequence ID No. 83 and the VL region shown in Sequence ID No. 84; k-1) The VH region shown in Sequence ID 91 and the VL region shown in Sequence ID 92; l-1) The VH region shown in Sequence ID 99 and the VL region shown in Sequence ID 100; m-1) The VH region shown in Sequence ID No. 107 and the VL region shown in Sequence ID No. 108; n-1) The VH region shown in Sequence ID No. 115 and the VL region shown in Sequence ID No. 116; o-1) The VH region shown in Sequence ID No. 123 and the VL region shown in Sequence ID No. 124; p-1) The VH region shown in Sequence ID No. 131 and the VL region shown in Sequence ID No. 132; q-1) The VH region shown in Sequence ID No. 139 and the VL region shown in Sequence ID No. 140; or r-1) The VH region shown in SEQ ID NO: 147 and the VL region shown in SEQ ID NO: 148, or s-1) The VH region shown in SEQ ID NO: 263 and / or the VL region shown in SEQ ID NO: 264.

[0142] In further embodiments, the polypeptide construct of the present invention includes a domain that binds to CLDN6, which contains any of the CDR regions shown in SEQ ID NOs: 680 to 694, for example, heavy chain CDR1 shown in SEQ ID NO: 680, or heavy chain CDR2 shown in SEQ ID NO: 681, or heavy chain CDR2 shown in SEQ ID NO: 682, or heavy chain CDR2 shown in SEQ ID NO: 683, or heavy chain CDR3 shown in SEQ ID NO: 684, or heavy chain CDR3 shown in SEQ ID NO: 685, or heavy chain CDR3 shown in SEQ ID NO: 686, or shown in SEQ ID NO: 687 The heavy chain CDR3, and / or the light chain CDR1 shown in SEQ ID NO: 688, the light chain CDR1 shown in SEQ ID NO: 689, the light chain CDR2 shown in SEQ ID NO: 690, the light chain CDR3 shown in SEQ ID NO: 691, the light chain CDR3 shown in SEQ ID NO: 692, the light chain CDR3 shown in SEQ ID NO: 693, and the light chain CDR3 shown in SEQ ID NO: 694, or any combination thereof including the heavy chain sequences shown in SEQ ID NOs: 680-687 and / or any combination thereof including the light chain sequences shown in SEQ ID NOs: 688-694. Those skilled in the art will know that the binding domain that binds to CLDN6 may include only one of HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 that may be present in the combination according to the present invention.

[0143] Other anti-CLDN6 conjugates were also analyzed for their CLDN6 binding specificity during epitope mapping (see Example 2). These CLDN6xCD3 antibody constructs were found to have different epitope specificities and were shown to have significantly lower cytotoxicity compared to the construct of the present invention. In Example 4, it was demonstrated that the construct of the present invention exhibited EC50 values ​​in the two-digit picomolar concentration range, while the comparative construct, despite having similar affinity for CLDN6, exhibited EC50 values ​​in the three- to five-digit picomolar concentration range. Constructs exhibiting the latter range of cytotoxic activity may not be sufficiently potent for therapeutic use to direct the cytotoxic activity of the patient's immune system, more specifically T cells, against cancer cells. On the other hand, the construct of the present invention exhibits a highly favorable epitope-activity relationship, thus supporting potent construct-mediated cytotoxic activity.

[0144] Whether an antibody, polypeptide construct, or paratope-containing domain (antigen-binding (epitope-binding) structure) binds to the same CLDN6 epitope on the surface of a target cell as another given antibody, construct, or binding domain can be measured by different analyses described herein, for example, by epitope mapping using the chimeric or mutant CLDN6 molecules described above or in Examples 1 and 2. Other epitope determination methods, such as alanine scanning, are described herein.

[0145] A domain containing an antibody, polypeptide construct, or paratope (antigen-binding (epitope-binding) structure) can be used to determine whether it competes with another given antibody or construct for binding to an antigen (such as CLDN6) on the surface of a target cell using a competitive assay such as a competitive ELISA. Avidin-conjugated microparticles (beads) may also be used. Similar to avidin-coated ELISA plates, each of these beads can be used as a substrate when reacting with biotinylated proteins, and the assay can be performed there. The beads are coated with the antigen and then pre-coated with a first antibody. A second antibody is added, and any additional binding is determined. Readout is performed by flow cytometry. Preferably, a cell-based competitive assay is used, either using cells that naturally express CLDN6 or cells that have been stably or transiently transformed with CLDN6. In this context, the term "competing for binding" means that, as determined by any one of the assays disclosed above, preferably a cell-based assay, competition occurs between two test antibodies at a rate of at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, or at least 90%. Of course, similar analyses can be applied to other targets such as CD3.

[0146] Competitive antibody / peptide construct binding assays include assays that determine the competitive binding of two antibodies / constructs to an antigen bound to a cell surface. A common method aims to detect the binding of two antibody / constructs A and B to the same antigen on the cell surface and may include the following steps: a) Cells are pre-incubated with antibody / polypeptide construct A, followed by the addition of labeled antibody / polypeptide construct B under maximum pressure. The binding of B is detected by comparing it to the binding in the absence of A, thereby blocking the cell surface antigen. b) Titration of antibody / polypeptide construct A in the presence of the lowest maximum amount of labeled antibody / polypeptide construct B (i.e., adding different amounts) and detection of the effect on binding of B, or c) Co-titration of A and B, i.e., a method unaffected by the order or relative amounts of antibody / construct addition, in which both antibody / polypeptide / polypeptide constructs are incubated together at their maximum concentrations and it is detected whether the total binding is equal to or greater than the binding of either A or B alone.

[0147] When two antibodies / polypeptides / polypeptide constructs A and B compete for an antigen bound to a cell surface, the antibodies very often compete in a blocking assay regardless of the order in which they are added. In other words, competition will be detected if the assay is performed in either direction. However, this is not always the case, and under certain circumstances, the order in which antibodies are added or the direction of the assay can affect the signal produced. This may be due to differences in affinity or avidity between potentially competing antibodies / constructs. If the order of addition has a significant effect on the signal produced, and competition is detected in at least one order, then it can be concluded that the two antibodies / constructs compete.

[0148] In relation to the present invention, the term "variable" refers to a portion of an antibody or immunoglobulin domain that exhibits variability in its sequence and is involved in determining the specificity and binding affinity of a particular antibody (i.e., a "variable region"). Typically, the heavy chain variable region (VH) and the light chain variable region (VL) come together as a pair to form a single antigen-binding site.

[0149] The variability is not uniformly distributed throughout the entire variable region of the antibody, but is concentrated in the subdomains of the heavy chain and light chain variable regions. These subdomains are called "hypervariable regions" or "complementarity-determining regions" (CDRs). The more conserved (i.e., non-hypervariable) portions of the variable region are called "framework" (FR) regions, and the six CDRs provide a three-dimensional scaffold for forming the antigen-binding surface. The variable regions of the heavy and light chains of naturally occurring antibodies each contain four FR regions (FR1, FR2, FR3, and FR4), primarily in a β-sheet configuration. Together with the CDRs, the FR regions form the following sequence within the variable heavy or variable light chain: FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4. The hypervariable regions of each chain are held together by the framework region and usually, together with the hypervariable region of the other chain, contribute to the formation of the antigen-binding site (see Kabat et al., cited above). When used herein, the polypeptide / polypeptide constructs of the present invention may have modifications in the framework region. These modifications may be substitutions of one or more amino acid residues of the sequences disclosed herein by other amino acid residues. Possible further modifications are deletions, inversions, and additions of amino acid residues, provided that these modifications do not interfere with the selective binding of the polypeptide / polypeptide construct to CLDN6 and / or do not interfere with the selective binding of the polypeptide / polypeptide construct to CLDN6-expressing target cells, and with the construct's ability to engage with and activate T cells and induce T cell-mediated cytotoxicity.Therefore, modifications to the framework region of the constructs disclosed herein, compared to non-framework-modified antibodies, engage T cells and induce T cell-mediated cytotoxicity in at least 100%, at least 99%, at least 98%, at least 97%, at least 96%, at least 95%, at least 94%, at least 93%, at least 92%, at least 91%, at least 90%, at least 89%, at least 88%, at least 87%, at least 86%, at least 85%, at least 84%, at least 83%. This still allows for capacities of at least 82%, at least 81%, at least 80%, at least 79%, at least 78%, at least 77%, at least 76%, at least 75%, at least 74%, at least 73%, at least 72%, at least 71%, at least 70%, at least 65%, at least 60%, at least 55%, at least 50%, at least 45%, at least 40%, at least 35%, at least 30%, at least 25%, at least 20%, at least 15%, at least 10%, and at least 5%. Modification in the framework region may also be associated with higher activity than the unmodified construct. It is also conceivable to modify the framework region of the construct of the present invention for purposes such as increasing the solubility of the construct in a given culture medium or increasing the stability of the construct.

[0150] The term "CDR" and its multiple counterparts refer to complementarity-determining regions, three of which constitute the binding properties of the light chain variable region (CDR-L1, CDR-L2, and CDR-L3), and three of which constitute the binding properties of the heavy chain variable region (CDR-H1, CDR-H2, and CDR-H3). Since CDRs contain most of the residues responsible for the specific interaction between the antibody (or construct or binding domain) and the antigen, they contribute to the functional activity of the antibody molecule; CDRs are the primary determinants of antigen specificity.

[0151] The precise definitions of CDR boundaries and lengths depend on different classification and numbering schemes. Therefore, CDRs may be referenced by any other boundary definition, including Kabat, Chothia, Contact, or the numbering systems described herein. Despite the different boundaries, each of these systems has some overlap in what constitutes the so-called "hypervariable regions" within the variable sequence. Thus, definitions of CDRs following these systems may differ in length and boundary regions with respect to adjacent framework regions. For example, Kabat (an approach based on interspecies sequence variability), Chothia (an approach based on crystallographic studies of antigen-antibody complexes), and / or MacCallum (see Kabat et al., op. cit.; Chothia et al., J.Mol.Biol, 1987, 196:901-917; and MacCallum et al., J.Mol.Biol, 1996, 262:732). Yet another criterion for characterizing antigen-binding sites is the AbM definition used by Oxford Molecular's AbM antibody modeling software. For example, see Protein Sequence and Structure Analysis of Antibody Variable Domains. In: Antibody Engineering Lab Manual (Ed.: Duebel, S. and Kontermann, R., Springer-Verlag, Heidelberg). As long as two residue identification techniques define overlapping but non-identical regions, they can be combined to define hybrid CDRs. However, numbering following the so-called Kabat system is preferred.

[0152] Typically, CDRs form loop structures that can be classified as canonical structures. The term "canonical structure" refers to the main chain conformation adopted by the antigen-binding (CDR) loop. Comparative structural studies have revealed that five of the six antigen-binding loops have only a limited repertoire of available conformations. Each canonical structure can be characterized by the twist angle of the polypeptide backbone. Therefore, corresponding loops between antibodies can have very similar three-dimensional structures despite high amino acid sequence variability in most of the loops (Chothia and Lesk, J.Mol.Biol., 1987, 196:901; Chothia et al., Nature, 1989, 342:877; Martin and Thornton, J.Mol.Biol., 1996, 263:800). Furthermore, there is a relationship between the adopted loop structure and the surrounding amino acid sequence. The conformation of a particular canonical class is determined by the length of the loop and the presence of amino acid residues at key positions within the loop and within the conserved framework (i.e., outside the loop). Therefore, assignment to a particular canonical class can be made based on the presence of these key amino acid residues.

[0153] The term “canonical structure” may also include considerations regarding the linear sequence of the antibody, as cataloged, for example, by Kabat (Kabat et al., cited above). The Kabat numbering scheme is a widely adopted standard for numbering amino acid residues in the antibody variable region in a consistent manner and is the preferred scheme applied in the present invention, as mentioned elsewhere in this specification. Further structural considerations may also be used to determine the canonical structure of the antibody. For example, these differences not fully reflected by Kabat numbering can be explained by the numbering system of Chothia et al., and / or revealed by other techniques, such as crystallography and two- or three-dimensional computational modeling. Thus, a given antibody sequence may be classified into a canonical class, in particular (for example, based on the requirement to include various canonical structures in a library) for which the identification of the appropriate class sequence is possible. Kabat numbering and structural considerations of antibody amino acid sequences, as described by Chothia et al. cited above, and their implications for constructing canonical aspects of antibody structures are described in the literature. The subunit structures and three-dimensional arrangements of various classes of immunoglobulins are well known in the art. For a review of antibody structures, see Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, eds. Harlow et al., 1988.

[0154] Light chain CDR3, and especially heavy chain CDR3, can constitute the most important determinants in antigen binding within the light chain variable region and the heavy chain variable region. In some antibodies or constructs / binding domains, the heavy chain CDR3 appears to constitute the primary contact area between the antigen and the antibody. In vitro selection schemes in which only the CDR3 is modified can be used to alter the binding properties of an antibody or construct / binding domain, or to determine which residues contribute to antigen binding. Therefore, CDR3 is typically the greatest source of molecular diversity within antibody binding sites. For example, CDR-H3 can be as short as two amino acid residues or more than 26 amino acids.

[0155] In classical full-length antibodies or immunoglobulins, each light (L) chain is linked to the heavy (H) chain by a single covalent disulfide bond, while the two H chains are linked to each other by one or more disulfide bonds, depending on the H chain isotype. The heavy chain constant (CH) domain closest to the VH is usually called CH1. The constant ("C") domain does not directly participate in antigen binding but exhibits various effector functions such as antibody-dependent cell-mediated cytotoxicity (ADCC) and complement activation (complement-dependent cytotoxicity, CDC). The Fc region of an antibody is the "tail" region of classical antibodies that interacts with cell surface receptors called Fc receptors and some proteins of the complement system. In IgG, IgA, and IgD antibody isotypes, the Fc region consists of two identical protein fragments derived from the second and third constant domains (CH2 and CH3) of the two heavy chains of the antibody. The Fc regions of IgM and IgE contain three heavy chain constant domains (CH2, CH3, and CH4) within each polypeptide chain. The Fc region also contains one or more disulfide and a portion of a so-called "hinge" region held together by non-covalent interactions. The Fc region of naturally occurring IgG carries a highly conserved N-glycosylation site. Glycosylation of the Fc fragment is essential for Fc receptor-mediated activity.

[0156] ADCC is a cell-mediated immune defense mechanism in which effector cells of the immune system actively lyse target cells, with their membrane surface antigens bound by specific antibodies. ADCC classically requires immune effector cells, typically natural killer (NK) cells that interact with IgG antibodies. However, ADCC can also be mediated by macrophages, neutrophils, and eosinophils. Naturally occurring ADCC involves activation of effector cells expressing Fc receptors by antibodies expressing the Fc region. For example, the most common Fc receptor on the surface of NK cells is called CD16 or FcγRIII. When the Fc receptor binds to the Fc region of IgG, NK cells release cytotoxic factors, leading to the death of target cells. Similarly, the Fc receptor on eosinophils (FceRI) recognizes IgE. In contrast, in CDC, the complement system molecule "C1q" binds to the antibody Fc region, and this binding triggers a complement cascade, which leads to the formation of membrane invasion complexes (MACs) on the surface of target cells as a result of classical pathway complement activation. In therapeutic antibodies, both ADCC and CDC can be modulated by Fc isotype engineering, Fc gene mutation, or modification of the Fc glycosylation profile. As used herein, the polypeptide / polypeptide constructs of the present invention do not induce ADCC as is generally understood. Instead, the polypeptides can engage T cells and induce T cell-mediated cytotoxicity, for example, by perforin secretion and / or induction of apoptosis.

[0157] The sequences of antibody genes after assembly and somatic mutation are highly diverse, and it is estimated that these diverse genes encode 10¹⁰ different antibody molecules (Immunoglobulin Genes, 2nd ed., eds. Jonio et al., Academic Press, San Diego, CA, 1995). Thus, the immune system provides a repertoire of immunoglobulins. The term “repertoire” refers to at least one nucleotide sequence that is derived, whole or partially, from at least one sequence encoding at least one immunoglobulin. Sequences may be generated by in vivo rearrangement of the V, D, and J segments of the heavy chain, and the V and J segments of the light chain. In addition, such sequences may be generated from cells in response to rearrangement-inducing stimuli, for example, in vitro stimuli. Alternatively, some or all of the sequences may be obtained by DNA splicing, nucleotide synthesis, mutagenesis, and other methods (see, for example, U.S. Patent No. 5,565,332). The repertoire may consist of only one sequence, or it may consist of multiple sequences that are part of a genetically diverse set.

[0158] The polypeptide construct of the present invention is envisioned to have a cysteine ​​clamp within the first domain. This cysteine ​​clamp may be introduced to improve the stability of the construct. See, for example, U.S. Patent Application Publication No. 2016 / 0193295.

[0159] In one embodiment of the present invention, the CLDN6-binding paratope (antigen-binding (epitope-binding) structure) of one domain of the construct of the present invention includes a VH region having the amino acid sequence shown in SEQ ID NO: 11, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, or SEQ ID NO: 193.

[0160] In further embodiments, the CLDN6-specific paratope, i.e., the antigen-binding (epitope-binding) domain of the construct of the present invention, includes a VL region having the amino acid sequence shown in SEQ ID NO: 12, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, or SEQ ID NO: 194.

[0161] In another embodiment, the CLDN6-specific paratope, i.e., the antigen-binding (epitope-binding) domain of the construct of the present invention, includes a VH region and a VL region having the amino acid sequence shown in SEQ ID NOs: 11+12(VH+VL), SEQ ID NOs: 25+26, SEQ ID NOs: 39+40, SEQ ID NOs: 67+68, or SEQ ID NOs: 193+194(VH+VL).

[0162] In further embodiments, the CLDN6-specific paratope, i.e., the antigen-binding (epitope-binding) domain of the construct of the present invention, includes a polypeptide having the amino acid sequence shown in SEQ ID NOs: 19, 22, 33, 36, 47, 50, 76, 78, 201, or 204, particularly SEQ ID NOs: 19 and 22.

[0163] As described above, the present invention provides embodiments in which the polypeptide construct is in a format selected from the group consisting of (scFv)2, scFv single-domain mAb, diabody, and oligomers of any of the above formats. The term “is in a format” does not preclude the construct from being further modified by binding or fusion to other parts, for example, as described herein. According to one embodiment of the polypeptide construct of the present invention, the paratope-containing domain described herein is in the format of scFv. In scFv, the VH region and the VL region are arranged in the order VH-VL or VL-VH (from N-terminus to C-terminus). It is assumed that the VH region and the VL region of the paratope-containing domain described herein are linked via a linker, preferably a peptide linker. According to one embodiment of the paratope-containing domain described herein, the VH region is located at the N-terminus of the linker and the VL region is located at the C-terminus of the linker. In other words, in one embodiment of the paratope-containing domain described herein, scFv includes: VH-linker-VL from N-terminus to C-terminus. The domains containing the paratopes described herein in the construct are further assumed to be linked via linkers, preferably peptide linkers. The construct may contain domains in the order of one domain-linker-second further domain (from N-terminus to C-terminus). The reverse order (further domain-linker-first domain) is also possible.

[0164] The linker is preferably a peptide linker, more preferably a short-chain peptide linker. According to the present invention, a “peptide linker” includes an amino acid sequence that links the amino acid sequence of one domain of the construct to the other (variable and / or binding) domain (e.g., the variable domain or the binding domain). An essential technical feature of such peptide linkers is that they are free from polymerization activity. Suitable peptide linkers are described in U.S. Patent Nos. 4,751,180 and 4,935,233 or International Publication No. 88 / 09344. Peptide linkers can also be used to link other domains, modules, or regions (such as half-life extension domains) to the construct of the present invention. Examples of useful peptide linkers are shown in Sequence IDs 563-575 and 679. In this context, a “short” linker has 2 to 50 amino acids, preferably 3 to 35, 4 to 30, 5 to 25, 6 to 20, or 6 to 17 amino acids. The linker between two variable regions of a single binding domain may have a different length (e.g., longer) than the linker between two binding domains. For example, the linker between two variable regions of a single binding domain may have a length of 7 to 15 amino acids, preferably 9 to 13, while the linker between two binding domains may have a length of 3 to 10 amino acids, preferably 4 to 8. The peptide linker is further assumed to be a glycine / serine linker, such as those shown in SEQ ID NOs. 563 to 575 and SEQ ID NO. 679. The majority of the amino acids in the glycine / serine linker are selected from glycine and serine.

[0165] When a linker is used, it is preferably of a length and sequence that ensures that each of the first and second domains can independently maintain their different binding specificities. For peptide linkers that connect at least two binding domains (or two variable regions forming one binding domain) in a construct, peptide linkers containing only a small number of amino acid residues, for example, 12 amino acid residues or less, are envisioned. Therefore, peptide linkers of 12, 11, 10, 9, 8, 7, 6, or 5 amino acid residues are preferred. Envisioned peptide linkers having fewer than 5 amino acids contain 4, 3, 2, or 1 amino acid, and glycy-rich linkers are preferred. In the context of "peptide linker," a "single amino acid" linker is glycy. Another embodiment of the peptide linker is characterized by the amino acid sequence Gly-Gly-Gly-Gly-Ser, i.e., Gly4Ser (SEQ ID NO: 563) or a polymer thereof, i.e., (Gly4Ser)x (wherein x is an integer of 1 or more (e.g., 2 or 3)). Available linkers are shown in SEQ ID NOs. 563-575 and SEQ ID NO: 679. The characteristics of peptide linkers are known in the art and are described, for example, in Dall'Acqua et al. (Biochem. (1998) 37, 9266-9273), Cheadle et al. (Mol Immunol (1992) 29, 21-30), and Raag and Whitlow (FASEB (1995) 9(1), 73-80). Peptide linkers that do not promote secondary structure are preferred. Linking of the domains to each other can be provided, for example, by genetic engineering. Methods for preparing fused and operably linked bispecific single-chain constructs and expressing them in mammalian cells or bacteria are known in the art (e.g., International Publication No. 99 / 54440 or Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 2001).

[0166] According to one embodiment of the present invention, the polypeptide construct of the present invention is a “single-chain construct.” It is also conceivable that either or both of the first or second binding domains may be in the form of a “single-chain Fv” (scFv). The two domains of the Fv fragment, VL and VH, are encoded by separate genes, but they can be linked by an artificial linker (as described above herein) which allows them to be constructed as a single protein chain paired so that the VL and VH regions form a monovalent molecule using recombination methods (see, for example, Huston et al. (1988) Proc. Natl. Acad. Sci USA 85:5879-5883). These antibody fragments are obtained using conventional techniques known to those skilled in the art, and the fragments are evaluated for function in the same manner as full-length antibodies or IgG. Thus, a single-chain variable fragment (scFv) is a fusion protein of the variable region (VH) of the heavy chain and the variable region (VL) of the light chain of an immunoglobulin, usually linked by a short linker peptide. The linker is typically rich in glycine for flexibility, and also rich in serine or even threonine for solubility, and can connect the N-terminus of VH to the C-terminus of VL, or vice versa. This protein retains the specificity of the original immunoglobulin despite the removal of the constant region and the introduction of the linker.

[0167] Bispecific single-chain molecules are known in the art and are described in International Publication No. 99 / 54440, Mack, J. Immunol. (1997), 158, 3965-3970, Mack, PNAS, (1995), 92, 7021-7025, Kufer, Cancer Immunol. Immunother., (1997), 45, 193-197, Loeffler, Blood, (2000), 95, 6, 2098-2103, Bruehl, Immunol., (2001), 166, 2420-2426, and Kipriyanov, J. Mol. Biol., (1999), 293, 41-56. Techniques described for producing single-chain constructs (see, in particular, U.S. Patent No. 4,946,778, Kontermann and Duebel (2010) and Little (2009) cited above) can be adapted to produce single-chain constructs that selectively, preferably, specifically recognize a selected target(s).

[0168] A bivalent (also called divalent) or bispecific single-chain variable fragment (bi-scFv or di-scFv) having a (scFv)2 configuration can be modified by linking two scFv molecules (e.g., by a linker as described above). This linking can be carried out by creating a single-chain polypeptide having two VH regions and two VL regions to generate a tandem scFv (see, for example, Kufer P. et al., (2004) Trends in Biotechnology 22(5):238-244). Another possibility is to create an scFv molecule with a linker peptide (e.g., about 5 amino acids) that is too short for the two variable regions to fold together, thereby forcing the scFv to dimerize. In this case, the VH and VL of the binding domain (which binds to either the target antigen CLDN6 or CD3) are not directly linked by a peptide linker. Therefore, the VH of the CD3-binding domain can, for example, fuse to the VL of the CLDN6-binding domain via a peptide linker, and the VH of the CLDN6-binding domain fuses to the VL of the CD3-binding domain via the corresponding peptide linker. This type is known as a diabody (see, for example, Hollinger, Philipp et al., (July 1993) Proceedings of the National Academy of Sciences of the United States of America 90(14):6444-8).

[0169] A construct called a “single-domain construct” (or sometimes “antibody construct”) contains a single (monomer) antibody variable region that can selectively bind to a specific antigen independently of other variable regions. The first single-domain antibodies were produced from heavy-chain antibodies found in camels, which are called VHH fragments. Cartilaginous fish also have heavy-chain antibodies (IgNARs) from which single-domain antibodies called VNAR fragments can be obtained. Another approach is to split the dimeric variable region from a common immunoglobulin into monomers, thus obtaining VH or VL as a single-domain Ab. Most research on single-domain antibodies is currently based on heavy-chain variable regions, but nanobodies derived from light chains have also been shown to bind specifically to target epitopes. Examples of single-domain antibodies are called sdAbs, nanobodies, or single variable-domain antibodies. Thus, (single-domain mAb)2 is a monoclonal construct consisting of (at least) two single-domain monoclonal constructs individually selected from the group including VH, VL, VHH, and VNAR. The linker is preferably in the form of a peptide linker. Similarly, "scFv-single-domain mAb" is a monoclonal antibody comprising at least one of the previously described single-domain antibodies and one of the previously described scFv molecules. Again, the linker is preferably in the form of a peptide linker.

[0170] Furthermore, the polypeptide constructs of the present invention are also expected to have additional functions in addition to their function of binding to the target molecules CLDN6 and CD3. In this format, the constructs may be triplicate or multifunctional constructs by providing further functions such as means or domains that target target cells through CLDN6 binding, mediate cytotoxic T cell activity through CD3 binding and enhance or prolong serum half-life, fully functional or modified Fc constant domains that mediate cytotoxicity through the recruitment of effector cells, labels (fluorescence, etc.), toxins, or therapeutic agents such as radionuclides.

[0171] Examples of means or domains for extending the serum half-life of polypeptide / polypeptide constructs of the present invention include peptide, protein, or protein domains that are fused to or otherwise attached to the polypeptide / polypeptide construct. The group of peptide, protein, or protein domains includes peptides that bind to other proteins having a favorable pharmacokinetic profile in the human body, such as serum albumin (see International Publication No. 2009 / 127691). An alternative concept for such half-life-extending peptides includes peptides that bind to the neonatal Fc receptor (FcRn, see International Publication No. 2007 / 098420), which can also be used in constructs of the present invention. The concept of attaching a larger domain or complete protein to a protein includes the fusion of human serum albumin, human serum albumin (see International Publication Nos. 2011 / 051489, 2012 / 059486, 2012 / 150319, 2013 / 135896, 2014 / 072481, and 2013 / 075066) or variants or mutants of that domain, as well as the fusion of the immunoglobulin constant region (Fc domain) and its variants. Such variants of the Fc domain are called Fc-based domains and may be optimized / modified, for example, to enable the desired pairing of dimers or multimers, to eliminate Fc receptor binding (e.g., to evade ADCC or CDC), or for other reasons. A further concept known in the art for extending the half-life of substances or molecules in the human body is the pegylation of those molecules (such as the constructs of the present invention).

[0172] In one embodiment, the polypeptide / polypeptide construct according to the present invention is linked (e.g., via a peptide bond) to a fusion partner (e.g., a protein, polypeptide, or peptide) to extend the serum half-life of the construct. These fusion partners can be selected from human serum albumin ("HSA" or "HALB") and its sequence variants, peptides that bind to HSA, peptides that bind to FcRn ("FcRn BP"), or constructs containing an (antibody-derived) Fc region. Exemplary sequences of these fusion partners are shown in SEQ ID NOs: 576-637. Generally, the fusion partner can be linked either directly (e.g., via a peptide bond) to the N-terminus or C-terminus of the construct according to the present invention, or via a peptide linker such as (GGGGS)n (wherein "n" is an integer of 2 or more, e.g., 2, 3, or 4). Suitable peptide linkers are discussed above and shown in SEQ ID NOs: 563-575.

[0173] Therefore, the polypeptide construct according to the present invention is assumed to include the following polypeptides, which are included in the following order from the N-terminus to the C-terminus. a) VL (containing part of the CLDN6-binding paratope)-(G4S)3-VH (containing part of the CLDN6-binding paratope)-peptide linker(SG4S)-VH (containing part of the CD3-binding paratope)-(G4S)3-VL (containing part of the CD3-binding paratope)-peptide linker(G4)-Fc monomer (part of the HLE domain)-(G4S)6-Fc monomer (part of the HLE domain); or b) VH (containing part of the CLDN6-binding paratope)-(G4S)3-VL (containing part of the CLDN6-binding paratope)-peptide linker(SG4S)-VH (containing part of the CD3-binding paratope)-(G4S)3-VL (containing part of the CD3-binding paratope)-peptide linker(G4)-Fc monomer (part of the HLE domain)-(G4S)6-Fc monomer (part of the HLE domain).

[0174] Therefore, the polypeptide construct according to the present invention is expected to include the following: (a) A polypeptide containing the following in the following order from the N-terminus to the C-terminus: Polypeptides having an amino acid sequence selected from the group consisting of SEQ ID NO: 12, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, and SEQ ID NO: 194; • A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 563, which can be replaced by any one of SEQ ID NOs: 564-575 or 679; and A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 11, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, and SEQ ID NO: 193. (b) A polypeptide containing the following in the following order from the N-terminus to the C-terminus: Polypeptides having an amino acid sequence selected from the group consisting of SEQ ID NOs: 11, 25, 39, 67, and 193; • A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 563, which can be replaced by any one of SEQ ID NOs: 564-575 or 679; and • A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 12, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, and SEQ ID NO: 194. (c) A polypeptide containing the following in the following order from the N-terminus to the C-terminus: Polypeptides having amino acid sequences selected from the group consisting of SEQ ID NO: 12 and SEQ ID NO: 194, particularly SEQ ID NO: 12; • A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 563, which can be replaced by any one of SEQ ID NOs: 564-575 or 679; and • A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 11 and SEQ ID NO: 193, particularly SEQ ID NO: 11. (d) A polypeptide containing the following in the following order from the N-terminus to the C-terminus: • Polypeptides having an amino acid sequence selected from the group consisting of SEQ ID NOs. 25, 39, and 67; · A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 563, which can be replaced by any one of SEQ ID NOs: 564 to 575 or 679; and · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 26, SEQ ID NO: 40, and SEQ ID NO: 68. (e) A polypeptide comprising the following in the following order from the N-terminus to the C-terminus. · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 12, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, and SEQ ID NO: 194; · A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 563, which can be replaced by any one of SEQ ID NOs: 564 to 575 or 679; and · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 11, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, and SEQ ID NO: 193. (f) A polypeptide comprising the following in the following order from the N-terminus to the C-terminus. · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 12, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, and SEQ ID NO: 194; · A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 563, which can be replaced by any one of SEQ ID NOs: 564 to 575 or 679; and · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 11, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, and SEQ ID NO: 193. · A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 565, which can be replaced by any one of SEQ ID NOs: 563, 564, 566 to 575 or 679; and · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NOs: 19, 22, 33, 36, 47, 50, 75, 78, 201, and 204, particularly SEQ ID NOs: 19 and 22. (g) A polypeptide comprising the following in the following order from the N-terminus to the C-terminus. [[ID=##]]· A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 11, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, and SEQ ID NO: 193; · A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 563, which can be replaced by any one of SEQ ID NO: 564 - 575; or 679; and · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 12, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, and SEQ ID NO: 194; · A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NO: 565, which can be replaced by any one of SEQ ID NO: 563, 564, 566 - 575; or 679; and · A polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 19, 22, 33, 36, 47, 50, 75, 78, 201, and 204, particularly 19 and 22.

[0175] According to another embodiment, the construct of the present invention includes an additional domain comprising two polypeptide monomers each containing a hinge, CH2, and CH3 domains (in addition to the domain containing the paratope described herein that binds to CLDN6 and CD3), and the two polypeptide monomers are fused to each other via a peptide linker. The third domain is envisioned to include, in order from the N - terminus to the C - terminus, hinge - CH2 - CH3 - linker - hinge - CH2 - CH3. The amino acid sequences that can be used for the third domain are shown in SEQ ID NO: 581 - 637. Each of the polypeptide monomers can have an amino acid sequence selected from the group consisting of SEQ ID NO: 630 - 637 or be at least 90% identical to those sequences.

[0176] One of the preferred polypeptide monomers is shown in SEQ ID NO: 622, and the preferred third domain is shown in SEQ ID NO: 630.

[0177] In another embodiment, the first and second domains of the construct of the present invention are fused to a third domain via a peptide linker selected from the group consisting of, for example, SEQ ID NOs: 563, 564, 565, 566, 567, 568, 569, 570, 571, 572, 573, 574, and 575 and SEQ ID NO: 679.

[0178] According to the present invention, the "hinge" is the IgG hinge region. This region can be identified by analogy using Kabat numbering (see, for example, Kabat positions 223-243). Consistent with the above, the minimum requirement for the "hinge" is the amino acid residues corresponding to the IgG1 sequence extension from D231-P243 according to Kabat numbering. The terms "CH2" and "CH3" refer to the constant regions 2 and 3 of the immunoglobulin heavy chain. These regions can also be identified by analogy using Kabat numbering; for example, see Kabat positions 244-360 for CH2 and Kabat positions 361-478 for CH3. It is understood that there is some variation among immunoglobulins with respect to the IgG1 Fc region, IgG2 Fc region, IgG3 Fc region, IgG4 Fc region, IgM Fc region, IgA Fc region, IgD Fc region, and IgE Fc region (see, for example, Padlan, Molecular Immunology, 31(3), 169-217 (1993)). In terminology, the Fc region refers to the last two heavy chain constant regions of IgA, IgD, and IgG, and the last three heavy chain constant regions of IgE and IgM. The Fc region may also contain the flexible hinge N-terminus to these domains. For IgA and IgM, the Fc region may include the J chain. In the case of IgG, the Fc region includes the immunoglobulin domains CH2 and CH3, and the hinge between the first two domains and CH2. The boundaries of the Fc region of immunoglobulins can vary, but one example of a human IgG heavy chain Fc portion containing the functional hinge, CH2 and CH3 domains can be defined as containing residues D231 (of the hinge domain) to P476 (of the C-terminus of the CH3 domain) or D231 to L476, respectively, in IgG4, with numbering following Kabat.

[0179] Therefore, the polypeptide construct of the present invention may include the following in the order from the N-terminus to the C-terminus: (a) A single domain containing a paratope (antigen-binding (epitope-binding) structure) that binds to the epitope of CLDN6; (b) A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs. 563-575, particularly 563, 568, 570-575, and more specifically SEQ ID NO. 570; (c) Another domain containing a paratope (antigen-binding (epitope-binding) structure) that binds to the CD3 epitope; (d) A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs. 563-575 and SEQ ID NO. 679, particularly SEQ ID NO. 679; (e) A polypeptide monomer having an amino acid sequence selected from the group consisting of SEQ ID NOs. 630-637, particularly SEQ ID NO. 630, and comprising a half-life extension domain (including hinge, CH2 and CH3 domains); (f) A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs. 563 to 575, particularly SEQ ID NO. 573; and (g) Another polypeptide monomer having an amino acid sequence selected from the group consisting of SEQ ID NOs. 630-637, particularly SEQ ID NO. 630, and having a half-life extension domain (including hinge, CH2 and CH3 domains).

[0180] The polypeptide construct of the present invention is assumed to include the following in the order from the N-terminus to the C-terminus: • One domain containing a paratope (antigen-binding (epitope-binding) structure) that binds to an epitope of CLDN6 having an amino acid sequence selected from the group consisting of SEQ ID NOs: 19, 22, 33, 36, 47, and more particularly SEQ ID NOs: 19 and 22 (the peptide linker contained within these sequences and having SEQ ID NO: 570 can be replaced with any one of SEQ ID NOs: 563-575); A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs: 563, 565, 566, 569, 570, and especially SEQ ID NO: 565; • Another domain containing a paratope (antigen-binding (epitope-binding) structure) that binds to the epitope of CD3 having an amino acid sequence selected from the group consisting of SEQ ID NOs. 542-562 and 678 (the peptide linkers contained within these sequences are selected from the amino acids having SEQ ID NOs. 563-575 and 679); • A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs. 563 to 575; and An additional domain comprising one or more amino acid sequences selected from the group consisting of SEQ ID NOs. 630-637, particularly SEQ ID NO. 630, and a peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs. 563-575, particularly SEQ ID NO. 573.

[0181] Therefore, in one embodiment, the polypeptide constructs of the present invention are SEQ ID NOs: 21, 24, 35, 38, 49, 52, 63, 66, 77, 80, 91, 94, 105, 108, 119, 122, 133, 136, 147, 150, 161, 164, 175, 178, 189, 192, 203, 206, 217, 220, 231, 234, 245, 148, 259, 262, 273, 276, 287, 290, 301, 304, 315, 3 A polypeptide comprising or consisting of amino acid sequences selected from the group 18, 329, 332, 343, 346, 357, 360, 371, 374, 385, 388, 399, 402, 413, 416, 427, and 430, in particular 21, 24, 35, 38, 49, 52, 63, 66, 77, 80, 91, 94, more particularly 21, 24, 35, 38, 49, 52, 77, and 80, in particular 21, 35, 49, and 77.

[0182] Covalent modifications of polypeptides / polypeptide constructs are also within the scope of the present invention, which are generally performed post-translation, though not necessarily. For example, some types of covalent modifications of constructs are introduced into the molecule by reacting specific amino acid residues of the construct with an organic derivatizing agent that can react with selected side chains or with N-terminal or C-terminal residues. Derivatization with bifunctional substances is useful for crosslinking the constructs of the present invention to water-insoluble support matrices or support surfaces for use in various ways. Glutaminyl and asparaginyl residues are often deamidated to their corresponding glutamyl and aspartyl residues, respectively. Alternatively, these residues are deamidated under weakly acidic conditions. Any form of these residues is within the scope of the present invention. Other modifications include hydroxylation of proline and lysine, phosphorylation of hydroxyl groups of ceryl or threonyl residues, methylation of α-amino groups of lysine, arginine, and histidine side chains (TECreighton, Proteins: Structure and Molecular Properties, WH Freeman & Co., San Francisco, 1983, pp. 79-86), acetylation of N-terminal amines, and amidation of any C-terminal carboxyl group.

[0183] Another type of covalent modification of constructs included in the scope of the present invention involves altering the glycosylation pattern of a protein. As is known in the art, the glycosylation pattern may depend on both the sequence of the protein (e.g., the presence or absence of certain glycosylated amino acid residues considered below) or on the host cell or organism in which the protein is produced. Specific expression systems are considered below. Polypeptide glycosylation is typically either N-linked or O-linked. N-linking refers to the attachment of the carbohydrate moiety to the side chain of an asparagine residue. The tripeptide sequences asparagine-X-serine and asparagine-X-threonine (wherein X is any amino acid except proline) are recognition sequences for the enzymatic attachment of the carbohydrate moiety to the asparagine side chain. Therefore, the presence of either of these tripeptide sequences in a polypeptide creates a potential glycosylation site. O-linked glycosylation refers to the linkage of one sugar, such as N-acetylgalactosamine, galactose, or xylose, to a hydroxyamino acid (most commonly serine or threonine), although 5-hydroxyproline or 5-hydroxylysine may also be used.

[0184] The addition of glycosylation sites to a construct is conveniently achieved by modifying the amino acid sequence to include one or more of the aforementioned tripeptide sequences (in the case of N-linked glycosylation sites). The modification can also be carried out by the addition or substitution of one or more serine or threonine residues to the starting sequence (for O-linked glycosylation sites). For convenience, the amino acid sequence of a construct can be modified through changes at the DNA level, particularly by mutating the polypeptide-encoding DNA with pre-selected bases to produce codons that will be translated into the desired amino acids.

[0185] Another means of increasing the number of sugar chains on a construct is by chemical or enzymatic binding of glycosides to the protein. These procedures are advantageous in that they do not require the production of proteins in host cells that have glycosylation capacity for N and O-linked glycosylation. Depending on the binding mode used, sugars can be bound to (a) arginine and histidine, (b) free carboxyl groups, (c) free sulfhydryl groups such as those of cysteine, (d) free hydroxyl groups such as those of serine, threonine, or hydroxyproline, (e) aromatic residues such as those of phenylalanine, tyrosine, or tryptophan, or (f) amide groups of glutamine. These methods are described in International Publication No. 87 / 05330 and Aplin and Wriston, 1981, CRC Crit. Rev. Biochem., pp. 259-306.

[0186] The removal of glycans present on the starting construct can be carried out chemically or enzymatically. Chemical deglycosylation requires exposure of the protein to the compound trifluoromethanesulfonic acid or an equivalent compound. This process results in the cleavage of almost all sugars except the linking sugars (N-acetylglucosamine or N-acetylgalactosamine) while leaving the polypeptide intact. Chemical deglycosylation is described by Hakimuddin et al., 1987, Arch. Biochem. Biophys. 259:52 and Edge et al., 1981, Anal. Biochem. 118:131. Enzymatic cleavage of the carbohydrate moiety on the polypeptide can be achieved by the use of various endoglycosidases and exoglycosidases, as described by Thotakura et al., 1987, Meth. Enzymol. 138:350. Glycosylation at potential glycosylation sites can be inhibited by the use of the compound tunicamycin, described by Duskin et al., 1982, J. Biol. Chem. 257:3105. Tunicamycin blocks the formation of protein-N-glycosidic bonds.

[0187] Other modifications of the construct are also contemplated herein. For example, another type of covalent modification of the construct involves linking the construct to various non-proteinaceous polymers including polyols in the manner shown in U.S. Patent Nos. 4,640,835; 4,496,689; 4,301,144; 4,670,417; 4,791,192 or 4,179,337. In addition, amino acid substitutions can be made at various positions within the construct, as is known in the art, to facilitate the addition of polymers such as polyethylene glycol (PEG).

[0188] In some embodiments, the covalent modification of the construct of the invention includes the addition of one or more labels. To reduce potential steric hindrance, the label group can be attached to the construct via spacer arms of various lengths. Various methods for labeling proteins are known in the art and can be used in practicing the present invention. The term "label" or "label group" refers to any detectable label. Generally, labels are classified into various classes depending on the assay in which they are detected, and examples include, but are not limited to, the following. a) Radioisotopes or radionuclides (e.g., 3 H, 14 C, 15 N, 35 S, 89 Zr, 90 Y, 99 Tc, 111 In, 125 I, 131 I) and other radioactive or heavy isotopes that can be isotope labels b) Magnetic labels (e.g., magnetic particles) c) Redox-active moieties d) Optical dyes (including, but not limited to, chromophores, phosphors and fluorophores), such as fluorescent groups (e.g., FITC, rhodamine, lanthanide phosphors), chemiluminescent groups and fluorophores that can be either "small molecule" fluorophores or proteinaceous fluorophores e) Enzyme groups (e.g., horseradish peroxidase, β-galactosidase, luciferase, alkaline phosphatase) f) Biotinylated groups g) Predetermined polypeptide epitopes recognized by secondary reporters (e.g., leucine zipper pairing sequences, binding sites of secondary antibodies, metal binding domains, epitope tags, etc.)

[0189] "Fluorescent label" means any molecule that can be detected through its inherent fluorescent properties. Suitable fluorescent labels include, but are not limited to: fluorescein, rhodamine, tetramethylrhodamine, eosin, erythrosine, coumarin, methylcoumarin, pyrene, malachite green, stilbene, lucifer yellow, Cascade BlueJ, Texas Red, IAEDANS, EDANS, BODIPY FL, LC Red 640, Cy 5, Cy 5.5, LC Red 705, Oregon Green, Alexa-Fluor dyes (Alexa Fluor 350, Alexa Fluor 430, Alexa Fluor 488, Alexa Fluor 546, Alexa Fluor 568, Alexa Fluor 594, Alexa Fluor 633, Alexa Fluor 660, Alexa Fluor 680), Cascade Blue, Cascade Yellow, and R-phycoerythrin (PE) (Molecular Probes, Eugene, OR), FITC, rhodamine, and Texas Red (Pierce, Rockford, IL), Cy5, Cy5.5, Cy7 (Amersham Life Science, Pittsburgh, PA). Suitable optical dyes containing fluorophores are described in the Molecular Probes Handbook by Richard P. Haugland.

[0190] Suitable protein-based fluorescent labels include green fluorescent protein, such as GFP (Chalfie et al., 1994, Science 263:802-805) and EGFP (Clontech Laboratories, Inc., Genbank® Accession No. U55762) from species of Renilla, Ptilosarcus, or Aequorea; blue fluorescent protein (BFP, Quantum Biotechnologies, Inc. 1801 de Maisonneuve Blvd. West, 8th Floor, Montreal, Quebec, Canada H3H 1J9; Stauber, 1998, Biotechniques 24:462-471; Heim et al., 1996, Curr. Biol. 6:178-182); and enhanced yellow fluorescent protein (EYFP, Clontech Laboratories, Inc.), luciferase (Ichiki et al., 1993, J.Immunol. 150:5408-5417), β-galactosidase (Nolan et al.) Examples include, but are not limited to, al., 1988, Proc. Natl. Acad. Sci. USA 85:2603-2607, and Renilla (International Publication No. 92 / 15673, International Publication No. 95 / 07463, International Publication No. 98 / 14605, International Publication No. 98 / 26277, International Publication No. 99 / 49019, U.S. Patent Nos. 5,292,658; 5,418,155; 5,683,888; 5,741,668; 5,777,079; 5,804,387; 5,874,304; 5,876,995; and 5,925,558).

[0191] Leucine zipper domains are peptides that promote the oligomerization of the proteins in which they are found. Leucine zippers were first identified in several DNA-binding proteins (Landschulz et al., 1988, Science 240:1759) and have since been found in a variety of different proteins. Known leucine zippers include naturally occurring peptides and their derivatives that dimerize or trimerize. Examples of leucine zipper domains suitable for producing soluble oligomeric proteins are described in PCT application international publication 94 / 10308 brochure, and a leucine zipper derived from lung surfactant protein D (SPD) is described in Hoppe et al., 1994, FEBS Letters 344:191. The use of modified leucine zippers that enable stable trimerization of heterologous proteins fused to them is described in Fanslow et al., 1994, Semin.Immunol.6:267-78.

[0192] The polypeptide constructs of the present invention may also include additional domains that, for example, aid in the isolation of the molecule or relate to the adaptation of the molecule's pharmacokinetic profile. Domains that aid in the isolation of the construct may be selected from peptide motifs that can be captured by isolation methods, such as isolation columns, or from secondarily introduced portions. Non-limiting embodiments of such further domains include peptide motifs known as Myc-tags, HAT-tags, HA-tags, TAP-tags, GST-tags, chitin-binding domains (CBD-tags), maltose-binding proteins (MBP-tags), Flag-tags, Strep-tags and their variants (e.g., StrepII-tags) and His-tags. All constructs disclosed herein, characterized by identified CDRs, may generally include His-tag domains known as consecutive His residues in the amino acid sequence of the molecule, for example, five His residues (SEQ ID NO: 638) or six His residues (hexahistidine, SEQ ID NO: 639). The His-tag may be located, for example, at the N-terminus or C-terminus of the construct. In one embodiment, a hexahistidine tag (HHHHHH) is linked to the C-terminus of the construct according to the present invention by a peptide bond.

[0193] Furthermore, the polypeptide construct of the present invention may include or consist of a polypeptide having an amino acid sequence selected from the group consisting of those shown in SEQ ID NOs. 22 and 24, and preferably linked to a protein purification tag at its N-terminus or C-terminus by a peptide bond (amide bond). Linking of the protein purification tag at the C-terminus of the polypeptide is preferred. The protein purification tag is expected to be a short-chain peptide. For example, the length of the short-chain peptide may be 2-30 amino acids, 4-25 amino acids, 5-20 amino acids, or 6-19 amino acids. Examples of protein purification tags include, but are not limited to, AU1 epitopes (e.g., as shown in SEQ ID NO: 644), AU5 epitopes (e.g., as shown in SEQ ID NO: 645), T7 tags (e.g., as shown in SEQ ID NO: 646), V5 tags (e.g., as shown in SEQ ID NO: 647), B tags (e.g., as shown in SEQ ID NO: 648), E2 epitopes (e.g., as shown in SEQ ID NO: 649), FLAG epitopes / FLAG tags (e.g., as shown in SEQ ID NO: 650), Glu-Glu tags (e.g., as shown in SEQ ID NO: 651 or 652), HA tags, histidine affinity tags (e.g., as shown in SEQ ID NO: 653), HSV epitopes (e.g., as shown in SEQ ID NO: 654), and KT3 epitopes (e.g., SEQ ID NO: 654). Examples include protein A (as shown in 55), Myc epitopes (e.g., as shown in SEQ ID NO: 656), polyarginine tags (5-6 Arg residues), polyaspartate tags (5-16 Asp residues), polyhistidine tags (2-10 His residues, usually 6 His residues, see SEQ ID NO: 639), polyphenylalanine tags (usually 11 Phe residues), S1 tags (e.g., as shown in SEQ ID NO: 659), S tags (e.g., as shown in SEQ ID NO: 660), Strep tags (e.g., as shown in SEQ ID NO: 661 or 662), universal tags (e.g., as shown in SEQ ID NO: 663), VSV-G (e.g., as shown in SEQ ID NO: 664), protein C (e.g., as shown in SEQ ID NO: 665), and protein A. Histidine tags, particularly 6xHis tags (SEQ ID NO: 639), are preferred.Therefore, it is further assumed that the construct of the present invention comprises a polypeptide having an amino acid sequence selected from the group consisting of those shown in SEQ ID NOs. 22 and 24, and linked to a 6xHis tag by a peptide bond at its C-terminus.

[0194] T cells, or T lymphocytes, are a type of lymphocyte (a type of white blood cell) that plays a central role in cellular immunity. Several subsets of T cells exist, each with distinct functions. T cells can be distinguished from other lymphocytes, such as B cells and NK cells, by the presence of a T cell receptor (TCR) on their cell surface. The TCR is involved in the recognition of antigens bound to major histocompatibility complex (MHC) molecules and is composed of two distinct protein chains. In 95% of T cells, the TCR consists of an alpha (α) chain and a beta (β) chain. When the TCR binds to the antigen peptide and MHC (peptide / MHC complex), the T lymphocyte is activated through a series of biochemical events mediated by related enzymes, co-receptors, specialized adapter molecules, and activated or released transcription factors.

[0195] The polypeptide construct of the present invention contains a domain that binds to CD3 on the surface of T cells. "CD3" (differentiation cluster 3) is a T cell coreceptor composed of four chains. In mammals, the CD3 protein complex contains a CD3γ (gamma) chain, a CD3δ (delta) chain, and two CD3ε (epsilon) chains. These four chains bind to the T cell receptor (TCR) and the so-called ζ (zeta) chain to form the "T cell receptor complex," which generates an activation signal in T lymphocytes. The CD3γ (gamma), CD3δ (delta), and CD3ε (epsilon) chains are highly related cell surface proteins of the immunoglobulin superfamily, each containing a single extracellular immunoglobulin domain. The intracellular tail of the CD3 molecule contains a single conserved motif known as the immunoreceptor tyrosine activation motif (ITAM), which is essential for TCR signaling ability. The CD3 epsilon molecule is a polypeptide encoded by the CD3 epsilon gene located on human chromosome 11. In the context of this invention, CD3 is understood as a protein complex and T cell coreceptor involved in the activation of both cytotoxic T cells (CD8+ naive T cells) and T helper cells (CD4+ naive T cells). It is typically composed of four distinct chains. In mammals in particular, the complex includes a CD3γ chain, a CD3δ chain, and two CD3ε chains. These chains associate with the T cell receptor (TCR) and the ζ chain (zeta chain) to generate an activation signal in T lymphocytes. The TCR, ζ chain, and CD3 molecule together constitute the TCR complex.

[0196] Target cell lysis redirected via T cell recruitment by constructs that bind CD3 on T cells and target proteins on target cells generally involves cytolytic synapse formation and delivery of perforins and granzymes. The associated T cells possess a range of target cell lysis capabilities and are unaffected by immune escape mechanisms that prevent peptide antigen processing and presentation or clonal T cell differentiation. See, for example, International Publication No. 2007 / 042261.

[0197] The cytotoxicity mediated by the CLDN6xCD3 construct can be measured by various methods. The "maximum half-volume effective concentration" (EC50) is commonly used as a measure of the potency of biologically active molecules, such as the construct of the present invention. This can be expressed in molar units. In this measurement of cytotoxicity, the EC50 value refers to the concentration of the construct that produces an intermediate cytotoxic response (lyse of target cells) between baseline and maximum. Effector cells in a cytotoxicity assay may be, for example, stimulated enriched (human) CD8-positive T cells or unstimulated (human) peripheral blood mononuclear cells (PBMCs). Typically, when stimulated / enriched CD8+ T cells are used as effector cells, the EC50 value can be expected to be lower compared to unstimulated PBMCs. If the target cells are macaque-derived, or express or transfected with macaque CLDN6, the effector cells must also be macaque-derived, such as a macaque T cell line, e.g., 4119LnPx. The target cells should express CLDN6, such as human or macaque CLDN6, on their cell surface. Preferably, the target cells should express at least one or more extracellular loops of CLDN6, such as CLDN6 loop 1 and / or loop 2, on their cell surface. The target cells may be cell lines (e.g., CHO) that have been stably or transiently transfected with CLDN6, such as human or macaque CLDN6. Alternatively, the target cells may be CLDN6-positive naturally expressing cell lines, such as human cancer cells. Typically, the EC50 value is expected to be lower when using target cells that express higher levels of CLDN6 on their cell surface compared to target cells with lower target expression rates.

[0198] The effector-to-target cell (E:T) ratio in cytotoxicity assays is typically around 10:1, but this can also vary. The cytotoxic activity of the CLDN6xCD3 construct can be measured in a 51-chromium release assay (e.g., with an incubation time of approximately 18 hours) or a FACS-based cytotoxicity assay (e.g., with an incubation time of approximately 48 hours). Modifications to the incubation time (cytotoxic response) are also possible. Other methods for measuring cytotoxicity are well known and include MTT or MTS assays, ATP-based assays including bioluminescence assays, sulforhodamine B (SRB) assays, WST assays, cloning assays, and ECIS technology.

[0199] According to one embodiment, the cytotoxic activity mediated by the CLDN6xCD3 construct of the present invention is measured in a cell-based cytotoxicity assay. This can also be measured in a 51-chromium release assay. The EC50 values ​​of the construct of the present invention are assumed to be ≤300pM, ≤280pM, ≤260pM, ≤250pM, ≤240pM, ≤220pM, ≤200pM, ≤180pM, ≤160pM, ≤150pM, ≤140pM, ≤120pM, ≤100pM, ≤90pM, ≤80pM, ≤70pM, ≤60pM, ≤50pM, ≤40pM, ≤30pM, ≤20pM, ≤15pM, ≤10pM, or ≤5pM.

[0200] The given EC50 values ​​above can be measured under different assays and conditions. For example, when human PBMCs are used as effector cells and CLDN6-transfected cells such as CHO cells are used as target cells, the EC50 values ​​of the CLDN6xCD3 construct are expected to be ≤500pM, ≤400pM, ≤300pM, ≤280pM, ≤260pM, ≤250pM, ≤240pM, ≤220pM, ≤200pM, ≤180pM, ≤160pM, ≤150pM, ≤140pM, ≤120pM, ≤100pM, ≤90pM, ≤80pM, ≤70pM, ≤60pM, ≤50pM, ≤40pM, ≤30pM, ≤20pM, ≤15pM, ≤10pM, or ≤5pM. When human PBMCs are used as effector cells and the target cells are CLDN6-positive cell lines, the EC50 values ​​of the CLDN6xCD3 construct are expected to be ≤300pM, ≤280pM, ≤260pM, ≤250pM, ≤240pM, ≤220pM, ≤200pM, ≤180pM, ≤160pM, ≤150pM, ≤140pM, ≤120pM, ≤100pM, ≤90pM, ≤80pM, ≤70pM, ≤60pM, ≤50pM, ≤40pM, ≤30pM, ≤20pM, ≤15pM, ≤10pM, or ≤5pM.

[0201] According to one embodiment, the CLDN6xCD3 polypeptide / polypeptide construct of the present invention does not induce or mediate the lysis of cells that do not express CLDN6 on their surface (CLDN6-negative cells), such as CHO cells, or does not inherently induce or mediate such lysis. The terms “does not induce lysis,” “does not inherently induce lysis,” “does not mediate lysis,” or “does not inherently mediate lysis” mean that the construct of the present invention does not induce or mediate the lysis of more than 30% of CLDN6-negative cells, preferably not more than 20%, more preferably not more than 10%, and particularly preferably not more than 9%, 8%, 7%, 6%, or 5% (where lysis of target cells expressing CLDN6 (such as cells transformed or transfected with CLDN6 or cell lines that are naturally expressing such cells, such as human cancer lines) is defined as 100%). This typically applies to construct concentrations up to 500 nM. Cell lysis measurement is a routine technique. Furthermore, this specification provides specific instructions for methods of measuring cell lysis.

[0202] The difference in cytotoxic activity between the monomeric and dimeric isoforms of individual CLDN6xCD3 polypeptide / polypeptide constructs is called the "potency gap." This potency gap can be calculated, for example, as the ratio of the EC50 value of the monomeric form of the molecule to the EC50 value of the dimeric form. One method for determining this gap involves performing an 18-hour 51-chromium release assay or a 48-hour FACS-based cytotoxicity assay on the purified construct monomer and dimer, as described later. Effector cells are stimulated enriched human CD8+ T cells or unstimulated human PBMCs. Target cells are hu CLDN6-transfected CHO cells. The effector-to-target cell (E:T) ratio is 10:1. The potency gap of the CLDN6xCD3 construct of the present invention is preferably ≤5, more preferably ≤4, even more preferably ≤3, even more preferably ≤2, and most preferably ≤1.

[0203] The domain of the polypeptide construct of the present invention is preferably interspecies-specific to members of the order Mammalia, such as macaques. An interspecies-specific CD3-binding domain is described, for example, in International Publication No. 2008 / 119567. According to one embodiment, in addition to binding to human CD3, the domain will also bind to CD3 of primates, including (but not limited to) New World primates (common marmoset (Callithrix jacchus), cotton-top tamarin (Saguinus Oedipus), or squirrel monkey (Saimiri sciureus), etc.), Old World primates (baboons and macaques, etc.), gibbons, orangutans, and non-human Homininae. The domain that binds to human CD3 on the surface of T cells is expected to bind to at least macaque CD3. A preferred macaque is the crab-eating macaque (Macaca fascicularis). The rhesus macaque (Macaca mulatta) is also considered. One construct of the present invention comprises a domain that binds to human CLDN6 on the surface of a target cell and another domain that binds to human CD3 and at least macaque CD3 on the surface of a T cell.

[0204] In one embodiment, the affinity gap of the construct according to the present invention with respect to binding to human CD3 compared to macaque CD3 [KD ma CD3:KD hu CD3] is 0.01 to 100, preferably 0.1 to 10, more preferably 0.2 to 5, more preferably 0.3 to 4, even more preferably 0.5 to 3 or 0.5 to 2.5, and most preferably 0.5 to 1 (as determined, for example, by BiaCore or scatchard analysis).

[0205] One domain of the construct of the present invention binds to CD3. More preferably, it binds to CD3 on the surface of T cells. It is further envisioned that the domain binds to human CD3 on the surface of T cells, preferably human CD3. It is also envisioned that the domain binds to CD3 epsilon. More preferably, it binds to human CD3 epsilon, for example, human CD3 epsilon on the surface of T cells. A preferred amino acid sequence for the extracellular domain of human CD3ε is shown in SEQ ID NO: 442.

[0206] In one embodiment of the present invention, the domain of the construct binds to human CD3 epsilon (or human CD3 epsilon on the surface of T cells) and common marmoset (Callithrix jacchus) or common squirrel monkey (Saimiri sciureus) CD3 epsilon. The domain is also envisioned to bind to the extracellular epitope of CD3 epsilon, preferably the extracellular epitope of human CD3 epsilon. The domain is also envisioned to bind to the extracellular epitopes of human and macaque CD3 epsilon chains. One preferred epitope of CD3ε is located within the range of amino acid residues 1-27 of the human CD3ε extracellular domain (see SEQ ID NO: 443). More specifically, the epitope includes at least the amino acid sequence Gln-Asp-Gly-Asn-Glu. The common marmoset (Callithrix jacchus) is a new species of primate belonging to the family Callitrichidae, while the common squirrel monkey (Saimiri sciureus) is a new species of primate belonging to the family Cebidae. Binding agents with these properties are described in detail in International Publication No. 2008 / 119567.

[0207] Antibodies or bispecific constructs against (human) CD3, or selectively, preferably specifically, against CD3 epsilon, are known in the art, and their CDR, VH, and VL sequences can serve as the basis for the binding domain of the polypeptide construct of the present invention. For example, in 1979, Kung et al. reported the development of OKT3 (Ortho Kung T3), the first mAb to recognize CD3 (specifically, the epsilon chain of CD3) on human T cells. OKT3 (muromonab) was the first mouse-derived monoclonal antibody to become available for therapeutic use in humans. Recent anti-CD3 monoclonal antibodies include otelixizumab (TRX4), teplizumab (MGA031), foralumab, and vizilizumab, all of which target the ε chain of CD3. Bispecific constructs targeting (cancer) targets and CD3 have also been developed and clinically tested, and their CD3-binding domains (CDR, VH, VL) may serve as the basis for the second binding domain of the constructs of the present invention. Examples, but not limited to, include blinatumomab, solitomab (MT110, AMG110), catumakisomab, duvortuxizumab, erzumakisomab, mosnetuzumab, FBTA05 (Bi20, TPBs05), CEA-TCB (RG7802, RO6958688), AFM11, and MGD006 (S80880). Other examples of CD3-binding domains are disclosed, for example, in U.S. Patent No. 7,994,289 B2, No. 7,728,114 B2, No. 7,381,803 B1, and No. 6,706,265 B1.

[0208] In the polypeptide construct used according to the present invention, the domain that binds to CD3 on the surface of a T cell includes a VL region containing CDR-L1, CDR-L2, and CDR-L3, the sequence of CDR-L1 is shown in SEQ ID NO: 673, the sequence of CDR-L2 is shown in SEQ ID NO: 674, and the sequence of CDR-L3 is shown in SEQ ID NO: 675, or the VL region includes CDR-L1, CDR-L2, and CDR-L3, and includes the CDR-L1 sequence shown in SEQ ID NO: 673, the CDR-L2 sequence shown in SEQ ID NO: 674, and the CDR-L3 sequence shown in SEQ ID NO: 675, where one or more of the CDRs have at least one amino acid residue modification.

[0209] The polypeptide construct used in accordance with the present invention comprises a domain that binds to CD3 on the surface of a T cell, comprising a VH region including CDR-H1, CDR-H2, and CDR-H3, and comprising the sequence of CDR-H1 shown in SEQ ID NO: 670, the sequence of CDR-H2 shown in SEQ ID NO: 671, and the sequence of CDR-H3 shown in SEQ ID NO: 672, or comprising a VH region including CDR-H1, CDR-H2, and CDR-H3, and comprising the sequence of CDR-H1 shown in SEQ ID NO: 670, the sequence of CDR-H2 shown in SEQ ID NO: 671, and the sequence of CDR-H3 shown in SEQ ID NO: 672, wherein one or more of the CDRs have at least one amino acid residue modification.

[0210] The polypeptide construct used in accordance with the present invention comprises a VL region including CDR-L1, CDR-L2, and CDR-L3, and a VH region including CDR-H1, CDR-H2, and CDR-H3, wherein the sequence of CDR-L1 is shown in SEQ ID NO: 673, the sequence of CDR-L2 is shown in SEQ ID NO: 674, the sequence of CDR-L3 is shown in SEQ ID NO: 675, and further, the sequences of CDR-H1 shown in SEQ ID NO: 670, CDR-H2 shown in SEQ ID NO: 671, and CDR-H3 shown in SEQ ID NO: 672 are assumed to bind to CD3. The conjugated domain includes a VL region containing CDR-L1, CDR-L2, and CDR-L3, and a VH region containing CDR-H1, CDR-H2, and CDR-H3, the sequence of CDR-L1 is shown in SEQ ID NO: 673, the sequence of CDR-L2 is shown in SEQ ID NO: 674, the sequence of CDR-L3 is shown in SEQ ID NO: 675, the sequence of CDR-H1 is shown in SEQ ID NO: 670, the sequence of CDR-H2 is shown in SEQ ID NO: 671, and the sequence of CDR-H3 is shown in SEQ ID NO: 672, and it is further assumed that one or more CDRs have at least one amino acid residue modification.

[0211] In the polypeptide construct used according to the present invention, it is assumed that the domain that binds to CD3 on the surface of T cells includes the VL region shown in Sequence ID No. 677, or that the VL region includes at least one amino acid residue modification.

[0212] In the polypeptide construct used according to the present invention, it is assumed that the domain that binds to CD3 on the surface of T cells includes the VH region shown in Sequence ID No. 676, or that the VH region includes at least one amino acid residue modification.

[0213] More preferably, the polypeptide construct used in accordance with the present invention is characterized by (a) a domain that binds to CD3 on the surface of a T cell, comprising a VL region and a VH region selected from the group consisting of the VL region shown in SEQ ID NO: 677 and the VH region shown in SEQ ID NO: 676, or the VL region or VH region comprises at least one amino acid residue modification.

[0214] A preferred embodiment of the polypeptide construct used in accordance with the present invention is characterized by a domain that binds to CD3 on the surface of a T cell, comprising the amino acid sequence shown in SEQ ID NO: 678, or the domain that binds to CD3 on the surface of a T cell, comprising the amino acid sequence shown in SEQ ID NO: 678, comprises at least one amino acid residue modification.

[0215] The polypeptide construct used in accordance with the present invention is expected to include a VL region (e.g., the VL region shown in SEQ ID NO: 540) or a VH region (e.g., the VL region shown in SEQ ID NO: 522 or 533), or a CDR shown in SEQ ID NOs: 444 to 506, particularly the CDRs shown in SEQ ID NOs: 480 to 482 and 504 to 506, or an scFv shown in, for example, SEQ ID NOs: 551 or 562, or any one of SEQ ID NOs: 542 to 561.

[0216] Amino acid sequence modifications of polypeptides / polypeptide constructs described herein are also intended. For example, it may be desirable to improve the binding affinity and / or other biological properties of the polypeptide construct. Amino acid sequence variants of polypeptides / polypeptide constructs are prepared by peptide synthesis or by introducing appropriate nucleotide changes into the nucleic acid molecule encoding the polypeptide / polypeptide construct. All of the amino acid sequence modifications described below should result in polypeptide constructs that retain the desired biological activity of the unmodified parent molecule (e.g., binding to CLDN6 and CD3, induction of cytotoxicity against CLDN6-positive target cells).

[0217] The terms “amino acid” or “amino acid residue” typically refer to amino acids having a recognized definition in the art, such as those selected from the group consisting of: alanine (Ala or A); arginine (Arg or R); asparagine (Asn or N); aspartic acid (Asp or D); cysteine ​​(Cys or C); glutamine (GIn or Q); glutamic acid (GIu or E); glycine (GIy or G); histidine (His or H); isoleucine (Ile or I); leucine (Leu or L); lysine (Lys or K); methionine (Met or M); phenylalanine (Phe or F); proline (Pro or P); serine (Ser or S); threonine (Thr or T); tryptophan (Trp or W); tyrosine (Tyr or Y); and valine (VaI or V) (modified amino acids, synthetic amino acids, or dilute amino acids may be used as needed). There are essentially four different classes of amino acids, determined by their different side chains. (1) Nonpolar and neutral (uncharged): Ala, Gly, Ile, Leu, Met, Phe, Pro, Val; (2) Polar and neutral (uncharged): Asn, Cys (slightly polar), Gln, Ser, Thr, Trp (slightly polar), Tyr; (3) Acidic and polar (negatively charged): Asp and Glu; (4) Basic and polar (positively charged): Arg, His, Lys.

[0218] Hydrophobic amino acids can be divided into those with aliphatic and those with aromatic side chains. Phe and Trp (highly hydrophobic), and Tyr and His (lowly hydrophobic) are classified as aromatic amino acids. Strictly speaking, aliphatic means that the side chain contains only hydrogen and carbon atoms. By this strict definition, amino acids with aliphatic side chains are alanine, isoleucine, leucine (also norleucine), proline, and valine. The fact that alanine's side chain is very short means that it is not particularly hydrophobic, and that proline has an unusual geometric shape that gives it a special role in proteins. Methionine, which also contains a sulfur atom, is often convenient to consider as being in the same category as isoleucine, leucine, and valine. The unifying theme is that these amino acids mainly contain non-reactive and flexible side chains. The amino acids alanine, cysteine, glycine, proline, serine, and threonine are often grouped together because they are all small. Gly and Pro can affect chain orientation.

[0219] Amino acid modifications include, for example, the deletion of residues from the amino acid sequence of an antibody construct, the insertion of residues into an antibody construct, and / or the substitution of residues within the amino acid sequence of a polypeptide / polypeptide construct. Any combination of deletions, insertions, and / or substitutions is provided to arrive at the final construct, provided that the final construct possesses the desired properties of the unmodified parent molecule, such as biological activity (binding to CLDN6 and CD3, induction of cytotoxicity against CLDN6-positive target cells, etc.). Amino acid changes can also alter the post-translational processes of the construct, such as changes in the number or location of glycosylation sites.

[0220] For example, in each CDR (depending on their respective lengths, of course), one, two, three, four, five, or six amino acids may be inserted, deleted, and / or substituted, while in each framework region (FR), one, two, three, four, five, six, seven, eight, nine, ten, eleven, twelve, thirteen, four, fifteen, six, seven, eight, nine, twenty, or twenty-five amino acids may be inserted, deleted, and / or substituted. Amino acid sequence insertions include, for example, N-terminal and / or C-terminal additions of amino acids in polypeptides ranging in length from one, two, three, four, five, six, seven, eight, nine, or ten residues to more than ten, for example, more than 100 residues, as well as intra-sequence insertions of single or multiple amino acid residues. Insertion variants of the constructs of the present invention include the fusion of polypeptides to the N-terminus or C-terminus of the construct to increase or extend the serum half-life of the construct. Such insertions may occur within the construct, for example, between a first domain and a second domain.

[0221] The most interesting sites for amino acid modification, and especially for amino acid substitution, are the hypervariable regions of the heavy and / or light chains, particularly individual CDRs, although modifications of the FR in the heavy and / or light chains are also intended. Substitutions may be conservative substitutions as described herein. Preferably, depending on the length of the CDR or FR, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids may be substituted in the CDR, and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or 25 amino acids may be substituted in the framework region (FR). For example, if the CDR sequence contains 6 amino acids, it is conceivable that 1, 2, or 3 of these amino acids may be substituted. Similarly, if the CDR sequence contains 15 amino acids, it is conceivable that 1, 2, 3, 4, 5, or 6 of these amino acids may be substituted.

[0222] A useful method for identifying specific residues or regions within a construct that are favorably located for mutagenesis is called "alanine scanning mutagenesis," and is described, for example, by Cunningham BC and Wells JA (Science. 1989 Jun 2; 244(4908): 1081-5). Here, a residue or group of residues within a construct is identified (e.g., charged residues such as Arg, His, Lys, Asp, and Glu), and the interaction of each amino acid with the epitope of the target protein is affected by its replacement with a neutral or nonpolar amino acid (most preferably alanine or polyalanine). Alanine scanning is a technique used to determine the contribution of a particular residue to the stability or function of a given protein. Alanine is used because of its low bulk and chemically inactive methyl functional group, which still mimics the secondary structure preference of many other amino acids. Occasionally, bulkier amino acids such as valine or leucine may be used when size preservation of the mutant residue is required. This technique may also be useful in determining whether the side chains of specific residues play a crucial role in biological activity. Alanine scanning is typically achieved by site-directed mutagenesis or randomly by PCR library creation. Furthermore, computational methods have been developed to estimate thermodynamic parameters based on theoretical alanine substitutions. The data can be tested by IR, NMR spectroscopy, mathematical methods, bioassays, etc.

[0223] Next, the amino acid site exhibiting functional sensitivity to the substitution (for example, determined by alanine scanning) can be purified by introducing further or other variants to or from the substitution site. Therefore, while the site or region to which the amino acid sequence mutation is introduced is predetermined, the nature of the mutation itself does not need to be predetermined. For example, to analyze or optimize the performance of a mutation at a given site, alanine scanning or random mutagenesis can be performed on the target codon or region, and the expressed construct variants can be screened for the optimal combination of desired activity. Well-known methods for introducing substitutional mutations at predetermined sites in DNA with known sequences include, for example, the M13 primer mutagenesis method and the PCR mutagenesis method. Screening of mutants can be performed, for example, using assays for antigen (e.g., CLDN6 or CD3) binding activity and / or cytotoxic activity.

[0224] Generally, when an amino acid is substituted in one, more, or all of the heavy chain and / or light chain CDRs, the resulting “substituted” sequence is assumed to be at least 60% or 65%, more preferably 70% or 75%, even more preferably 80% or 85%, and particularly preferably 90% or 95% identical / homological to the “original” or “parent” CDR sequence. This means that the degree of identity / homology between the original sequence and the substituted sequence depends on the length of the CDR. For example, a CDR having a total of 5 amino acids and containing one amino acid substitution is 80% identical to the “original” or “parent” CDR sequence, while a CDR having a total of 10 amino acids and containing one amino acid substitution is 90% identical to the “original” or “parent” CDR sequence. Therefore, the substituted CDRs of the constructs of the present invention may have different degrees of identity with respect to their original sequences; for example, CDRL1 may have 80% homology, while CDRL3 may have 90% homology. The same considerations apply to the framework domain, as well as the VH and VL domains as a whole.

[0225] A "variant CDR" is a CDR having specific sequence homology, similarity, or identity with the parent CDR of the present invention, and sharing biological function with the parent CDR by at least 60%, 65%, 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of the parent CDR, without limiting its specificity and / or activity. Generally, the amino acid homology, similarity, or identity between individual variant CDRs is at least 60% with respect to the parent sequence shown herein, more typically at least 65% or 70%, preferably at least 75% or 80%, more preferably at least 85%, 90%, 91%, 92%, 93%, 94%, and most preferably 95%, 96%, 97%, 98%, 99%, and nearly 100% increased homology, similarity, or identity. The same applies to "variant VH" and "variant VL". According to one embodiment, sequence mutations within "variant VH" and / or "variant VL" do not extend to the CDR. Therefore, the present invention relates to a construct as defined herein, comprising VH and VL sequences having specific sequence homology (see above) with respect to a specific sequence ("parent" VH and VL) as defined herein, wherein the CDR sequence is 100% identical to the specific CDR sequence ("parent" CDR) as defined herein.

[0226] The preferred substitution (or replacement) is a conservative substitution. However, any substitution (including non-conservative substitutions or one or more of the “exemplary substitutions” listed in Table 1 below) is conceivable, provided that the construct retains its ability to bind to CLDN6 by the first domain and to CD3 or CD3ε by the second domain, and / or that its CDR, FR, VH and / or VL sequences have at least 60% or 65%, more preferably at least 70% or 75%, even more preferably at least 80% or 85%, and particularly preferably at least 90% or 95% identity with the original sequence or parent sequence.

[0227] Conservative substitutions (also called conservative mutations or conservative substitutions) are amino acid substitutions that replace a given amino acid with a different amino acid that has similar biochemical properties (e.g., charge, hydrophobicity, size). Conservative substitutions of proteins often have less impact on protein function than non-conservative substitutions. Conservative substitutions are shown in Table 1. Exemplary conservative substitutions are indicated as “exemplary substitutions.” When such substitutions result in changes in biological activity, more substantial changes can be introduced with respect to amino acid classes, as further described herein, and the product can be screened for desired characteristics.

[0228] [Table 1]

[0229] Substantial modification of the biological properties of the constructs of the present invention is achieved by selecting substitutions that have a significantly different effect on (a) the structure of the polypeptide backbone around the substitution, e.g., sheet or helical structure, (b) the molecular charge or hydrophobicity at the target site, or (c) the maintenance of the bulk of the side chain. Non-conservative substitutions typically involve exchanging one member of one of the above-defined amino acid classes (e.g., polar, neutral, acidic, basic, aliphatic, aromatic, minor, etc.) with another class. The oxidative stability of the construct can be improved by generally substituting any cysteine ​​residue that does not contribute to maintaining the correct three-dimensional structure of the construct with serine.

[0230] The sequence identity, homology, and / or similarity of amino acid sequences are determined using standard techniques known in the art (e.g., local sequence identity algorithm of Smith and Waterman, 1981, Adv. Appl. Math. 2:482, sequence identity alignment algorithm of Needleman and Wunsch (J Mol Biol. 1970 Mar; 48(3): 443-53), similarity search method of Pearson and Lipman (Proc Natl Acad Sci USA. 1988 Apr; 85(8): 2444-8), computer execution of these algorithms (GAP, BESTFIT, FASTA, and TFASTA of Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis), and Develeux et al. (NucleicAcidsRes. 1984 Jan 11; 12(1 Pt). The identity percentage is determined using (1):387-95)) or by visual inspection. The identity percentage is expected to be calculated by FastDB based on the following parameters: mismatch penalty 1; gap penalty 1; gap size penalty 0.33; and join penalty 30. See also “Current Methods in Sequence Comparison and Analysis,” Macromolecule Sequencing and Synthesis, Selected Methods and Applications, pp 127-149 (1988), Alan R. Liss, Inc.

[0231] One example of a useful algorithm is PILEUP. PILEUP uses progressive pairwise alignment to create multiple sequence alignments from a group of related sequences. It can also plot a tree showing the clustering relationships used to create the alignments. PILEUP employs a simplified version of the progressive alignment method described by Feng and Doolittle (J Mol Evol. 1987;25(4):351-60). This method is similar to that described by Higgins and Sharp (Comput Appl Biosci. 1989 Apr;5(2):151-3). Useful PILEUP parameters include a default gap weight of 3.00, a default gap length weight of 0.10, and weighted end gaps.

[0232] Another example of a useful algorithm is the BLAST algorithm described in Altschul et al. (J Mol Biol. 1990 Oct 5;215(3):403-10.); Altschul et al., (Nucleic Acids Res. 1997 Sep 1;25(17):3389-402); and Karlin and Altschul (Proc Natl Acad Sci USA. 1993 Jun 15;90(12):5873-7). A particularly useful BLAST program is the WU-Blast-2 program, which was derived from Altschul et al. (Methods Enzymol. 1996;266:460-80). WU-Blast-2 uses several search parameters, most of which are set to default values. The adjustable parameters are set to the following values: overlap range = 1, overlap rate = 0.125, word threshold (T) = 11. The HSP S and HSP S2 parameters are dynamic values, established by the program itself depending on the composition of a particular sequence and the composition of each database in which the target sequence is being searched; however, the values ​​may be adjusted to increase sensitivity.

[0233] An additional useful algorithm is gapped BLAST, as reported by Altschul et al. (Nucleic Acids Res. 1997 Sep 1;25(17):3389-402). Gapped BLAST uses BLOSUM-62 substitution scores, with the threshold T parameter set to 9, a two-hit method to induce non-gap expansion, a charge gap length k costing 10+k; Xu is set to 16, and Xg is set to 40 for the database search phase of the algorithm and 67 for the output phase. Gapped alignment is caused by scores corresponding to approximately 22 bits.

[0234] In accordance with this specification, the term “percent (%) nucleic acid sequence identity / homologousity / similarity” with respect to nucleic acid sequences encoding constructs identified herein is defined as the percentage of nucleotide residues in a candidate sequence that are identical to nucleotide residues in the construct coding sequence. One method for aligning two sequences and thereby determining their homology is to use the BLASTN module of WU-Blast2 with default parameter settings, where the overlap span and overlap fraction are set to 1 and 0.125, respectively. Generally, the homology, similarity, or identity of nucleic acid sequences between the nucleotide sequences encoding individual variant CDRs and the nucleotide sequences shown herein is at least 60%, and more typically, at least 65%, 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99%, and increased homology, similarity, or identity of nearly 100%. Hereinafter, the same applies to the nucleic acid sequences encoding "variant VH" and / or "variant VL".

[0235] In one embodiment, the percentage of identity to the human germline of the polypeptide / polypeptide construct according to the present invention, or the domain containing the paratope (antigen-binding (epitope-binding) structure; (binding domain)) of these constructs, is 70% or more, 75% or more, more preferably 80% or more, 85% or more, even more preferably 90% or more, most preferably 91% or more, 92% or more, 93% or more, 94% or more, 95% or more, or 96% or more. Identity to human antibody germline gene products is considered an important feature for reducing the risk that therapeutic proteins will induce an immune response to the drug in patients during treatment. Hwang WY and Foote J. (Methods. 2005 May; 36(1): 3-10) have demonstrated that reducing the non-human portion of a drug construct results in a reduced risk of inducing anti-drug antibodies in patients during treatment. By comparing a comprehensive number of clinically evaluated antibody drugs with their respective immunogenicity data, humanization of the variable region of an antibody / construct tends to result in lower protein immunogenicity (average 5.1% of patients) compared to antibodies / constructs with an unaltered non-human variable region (average 23.59% of patients). Therefore, a higher degree of identity to the human sequence is desirable for protein therapeutics in the form of polypeptides / polypeptide constructs based on the variable region. To determine germline identity, the V region of the VL can be aligned with the amino acid sequences of human germline V and J segments (http: / / www2.mrc-lmb.cam.ac.uk / vbase / ) using Vector NTI software, as well as the amino acid sequence calculated by dividing identical amino acid residues by the total number of amino acid residues in the VL as a percentage. The same can be done for the VH segment (http: / / www2.mrc-lmb.cam.ac.uk / vbase / ), except that VH CDR3 may be excluded due to its high diversity and the lack of existing human germline VH CDR3 alignment partners. Next, recombinant technology can be used to enhance sequence identity for human antibody germline genes.

[0236] In further embodiments, the polypeptide / polypeptide constructs of the present invention exhibit high monomer yields under standard research-scale conditions, for example, in a standard two-step purification process. The monomer yield of the constructs according to the present invention is assumed to be ≥0.25 mg / L supernatant (SN), preferably ≥0.5 mg / L SN, more preferably ≥1 mg / L SN, even more preferably ≥2 mg / L SN, and most preferably ≥3 mg / L SN. The yield of the construct referred to as "CL-1xI2C-6His" has been shown to be 4.1 mg / L supernatant, and the yield of the construct referred to as "CL-1xI2C-scFc" has been shown to be 36.5 mg / L supernatant.

[0237] Similarly, the yield of dimer antibody construct isoforms of polypeptide constructs and therefore the monomer ratio (i.e., monomer:(monomer + dimer) of the construct) can be determined. The productivity of monomer and dimer constructs and the calculated monomer percentage can be obtained, for example, in an SEC purification step of the culture supernatant from standardized study-scale production in roller bottles. According to one embodiment, the monomer percentage of the construct of the present invention is ≥80%, more preferably ≥85%, even more preferably ≥90%, and most preferably ≥95%.

[0238] According to one embodiment, the polypeptide / polypeptide construct of the present invention has plasma stability (ratio of EC50 with plasma to EC50 without plasma) of ≤5 or ≤4, more preferably ≤3.5 or ≤3, even more preferably ≤2.5 or ≤2, and most preferably ≤1.5 or ≤1. The plasma stability of the construct can be tested by incubating the purified construct in human plasma at a concentration of, for example, 2 to 20 μg / ml at 37°C for 24 to 96 hours, followed by 18 hours of 51-chromium release or 48 hours of FACS cytotoxicity assay (e.g., the example portion). Effector cells in the cytotoxicity assay may be stimulated enriched human CD8-positive T cells (preferably) or unstimulated human PBMCs. Target cells may be, for example, CHO cells transfected with human CLDN6. The effector-to-target cell (E:T) ratio may be 10:1. The starting concentration of the construct in the cytotoxicity assay may be 0.01 to 0.1 μg / ml. The human plasma pool used for this purpose is derived from the blood of healthy donors collected using EDTA-coated syringes. Cellular components are removed by centrifugation, and the upper plasma phase is collected and subsequently pooled. As a control, the unincubated construct is diluted and immediately subjected to a cytotoxic assay in a suitable medium such as RPMI-1640. Plasma stability is calculated as the ratio of EC50 (after plasma incubation) to EC50 (control / unincubated).

[0239] Furthermore, the monomer-to-dimer conversion rate of the constructs of the present invention is expected to be low. The conversion can be measured under different conditions and analyzed by high-speed size exclusion chromatography. See Example 8. For example, incubation of the monomer isoform of the construct can be carried out in an incubator in a general formulation buffer at a concentration of, for example, 100 μg / ml or 250 μg / ml at 37°C for 7 days, followed by the determination of the percentage of constructs that were initially monomers converted to dimer constructs by high-performance SEC. Under these conditions, the polypeptide / polypeptide constructs of the present invention are expected to exhibit a dimer percentage of ≤8%, preferably ≤6%, more preferably ≤5%, more preferably ≤4%, even more preferably ≤3%, even more preferably ≤2.5%, even more preferably ≤2%, even more preferably ≤1.5%, and most preferably ≤1%, ≤0.5%, or even 0%.

[0240] Similarly, the polypeptide / polypeptide constructs of the present invention are expected to exhibit extremely low dimerization rates even after several freeze / thaw cycles. For example, a construct monomer is adjusted to a concentration of, for example, 250 μg / ml in a general formulation buffer, subjected to three freeze / thaw cycles (freezing at -80°C for 30 minutes, followed by thawing at room temperature for 30 minutes), and then high-performance SEC is performed to determine the percentage of the initial monomer construct converted to a dimer construct. The dimerization percentage of the construct is expected to be, for example, ≤8%, preferably ≤6%, more preferably ≤5%, more preferably ≤4%, even more preferably ≤3%, even more preferably ≤2.5%, even more preferably ≤2%, even more preferably ≤1.5%, and most preferably ≤1%, ≤0.5%, or even 0% after three freeze / thaw cycles.

[0241] According to one embodiment, the polypeptide / polypeptide construct of the present invention exhibits preferred thermal stability at aggregation temperatures of 45°C or higher, 46°C or higher, more preferably 47°C or higher, 48°C or higher, even more preferably 49°C or higher, 50°C or higher, and most preferably 51°C or higher. The thermal stability parameter can be determined with respect to the antibody aggregation temperature as follows: An antibody solution at a concentration of 250 μg / ml is transferred to a single-use cuvette and placed in a dynamic light scattering (DLS) instrument. The sample is heated from 40°C to 70°C at a heating rate of 0.5°C / min while maintaining a constant measured range. The increase in the range showing protein melting and aggregation is used to calculate the antibody aggregation temperature.

[0242] Alternatively, the melting temperature curve can be measured by differential scanning calorimetry (DSC) to determine the intrinsic biophysical protein stability of the construct. Such experiments can be performed using a MicroCal LLC VP-DSC instrument. The energy uptake of a sample containing the construct is recorded from 20°C to 90°C and compared with a sample containing only the formulation buffer. The construct is adjusted to a final concentration of, for example, 250 μg / ml in SEC running buffer. The temperature of the entire sample is increased stepwise to record each melting curve. The energy absorption of the sample and the formulation buffer reference at each temperature is recorded. The difference in energy uptake Cp (kcal / mol / °C), obtained by subtracting the reference from the sample, is plotted against each temperature. The melting temperature is defined as the temperature at the first maximum value of energy uptake.

[0243] The polypeptide / polypeptide constructs of the present invention are also expected to have a turbidity of ≤0.2 or ≤0.15, preferably ≤0.10 or ≤0.08, more preferably ≤0.06 or ≤0.05, and most preferably ≤0.04 or ≤0.03. Turbidity can be measured by OD340 at a construct concentration of 2.5 mg / ml and incubation at 5°C for 16 hours.

[0244] The change in the potency of a targeted xCD3 construct as a function of pre-incubation of the construct on target cells in the absence of T cells can be measured. If the construct is internalized, it is expected to undergo lysosomal degradation. Therefore, the effective concentration is expected to decrease over time, and thus the apparent potency should also decrease. This effect has been observed with several targets and is a known phenomenon. The construct of the present invention is assumed to be either not internalized or not undergo significant internalization by target cells. The rate of internalization can be assayed, for example, as described below. Count T cells and dilute them to a concentration of 1 x 10⁵ / ml in assay medium. Count target-positive target cells and seed them, for example, at 2500 cells per well (cpw). Serially dilute the construct 1:2 at a starting concentration, for example, 100 nM. Add the construct to a culture assay plate to allow incubation for 0, 1, or 2 hours before adding T cells. Next, T cells are plated with 25,000 cpw (E:T = 10:1), and the assay is incubated at 37°C for 48 hours. Target cell viability is analyzed, for example, using a Steady-Glo® system (25 μl / well). Preferably, the internalization rate (e.g., measured as a decrease in cytotoxicity) is ≤ 20%, more preferably ≤ 15%, even more preferably ≤ 10%, and most preferably ≤ 5% after 2 hours of (pre)incubation of the construct with target cells.

[0245] Further considerations include polypeptide constructs of the present invention in which the loss or soluble target does not significantly impair their efficacy or biological activity. This can be measured, for example, by a cytotoxic assay in which the soluble target is added to the assay at progressively increasing concentrations, e.g., 0 nM to 0.3 nM to 0.7 nM to 1 nM to 3 nM to 7 nM to 12 nM. An exemplary E:T value is 10:1. The EC50 value of the tested construct should not be significantly increased in the presence of the soluble target.

[0246] The EC50 values ​​of the polypeptide / polypeptide constructs of the present invention can be compared in an in vitro cytotoxicity assay using CLDN6-expressing cells (e.g., CHO cells expressing CLDN6 used as the target) and CLDN9-expressing cells (e.g., CHO cells expressing CLDN9 used as the target), with the latter serving as a negative control. The selectivity and specificity of the polypeptide / polypeptide constructs of the present invention can be determined using T cells (e.g., PBMCs) as effector cells and the above-mentioned CHO cells as targets. The cytotoxic effect of the polypeptide / polypeptide constructs of the present invention can be determined. According to the present invention, the polypeptide / polypeptide constructs described herein are at least 500-fold, at least 1000-fold, at least 2000-fold, preferably at least 3000-fold more effective against CLDN6-positive target cells than against CLDN9-positive target cells, and the targets are preferably of the same cell origin, e.g., CHO cells, that are transfected or transformed with genes encoding CLDN6 and CLDN9, respectively, and express them. Of course, other cell types expressing CLDN6, and control cells that do not express CLDN6 but express CLDN9 or CLDN4, or control cells that do not express any CLDN family members at all, can be used. These cells may be cell lines that naturally express the molecule of interest, or they may be genetically modified to express CLDN6 and / or other CLDN molecules, the latter being controls. These cells can be used in a method for determining T cell-dependent cytotoxicity associated with the polypeptide / polypeptide construct of the present invention.

[0247] In further embodiments, the polypeptide constructs according to the present invention are stable at acidic pH. The more tolerant the construct is of non-physiological pH, such as pH 5.5 (e.g., the pH required for cation exchange chromatography), the higher the recovery rate of the construct eluted from the ion exchange column relative to the total amount of loaded protein. The recovery rate of the construct from the ion (e.g., cation) exchange column at pH 5.5 is preferably 30% or more, more preferably 40% or more, more preferably 50% or more, even more preferably 60% or more, even more preferably 70% or more, even more preferably 80% or more, and most preferably 95% or more. The percentages represent the area under the curve (=AUC) of the major peak.

[0248] The polypeptide / polypeptide constructs of the present invention are further expected to exhibit therapeutic efficacy manifested as antitumor activity or tumor growth inhibition. This can be evaluated, for example, in tests as disclosed in Example 13 or 14. In one embodiment, the tumor growth inhibition T / C [%] of the constructs of the present invention is 70 or less, 60 or less, 50 or less, 40 or less, 30 or less, 20 or less, 10 or less, 5 or less, 4 or less, 3 or less, or 2 or less. Modifications or adjustments to specific parameters of these studies (e.g., number of tumor cells injected, injection site, number of transplanted human T cells, number of constructs administered, and timeline) are also expected, but significant and reproducible results can still be obtained.

[0249] The present invention further provides polynucleotide / nucleic acid molecules encoding polypeptide constructs of the present invention. Nucleic acid molecules are biopolymers composed of nucleotides. Polynucleotides are biopolymers composed of 13 or more nucleotide monomers covalently linked in a chain. DNA (cDNA, etc.) and RNA (mRNA, etc.) are examples of polynucleotide / nucleic acid molecules having different biological functions. Nucleotides are organic molecules that function as monomers or subunits of nucleic acid molecules such as DNA or RNA. The nucleic acid molecules or polynucleotides of the present invention may be double-stranded or single-stranded, linear or cyclic. It is envisioned that the nucleic acid molecules or polynucleotides will be contained in a vector. It is further envisioned that such vectors will be contained in host cells. Host cells can express constructs after transformation or translocation with, for example, the vector or polynucleotide / nucleic acid molecule of the present invention. For this purpose, the polynucleotide or nucleic acid molecule is operably linked to a control sequence.

[0250] The genetic code is a set of rules for translating information encoded within genetic material (nucleic acids) into proteins. In living cells, biological decoding is performed by ribosomes, which use tRNA molecules to carry amino acids and read three nucleotides of mRNA at once, linking them in the order specified by the mRNA. This code defines how a sequence of three nucleotides, called a codon, specifies which amino acid will be added next during protein synthesis. With some exceptions, a three-nucleotide codon in a nucleic acid sequence specifies one amino acid. Because most genes are encoded by the exact same code, this particular code is often referred to as the reference genetic code or standard genetic code.

[0251] Codon degeneracy is the redundancy of the genetic code, expressed as a large number of 3-base pair codon combinations that specify amino acids. Degeneracy arises because there are more codons than amino acids that can be coded. Codons that code for a single amino acid can differ in any of their three positions; however, often this difference is in the second or third position. For example, codons GAA and GAG both code for glutamic acid and exhibit redundancy, but neither specifies any other amino acid and therefore does not exhibit ambiguity. The genetic codes of different organisms may be biased towards using one of several codons that code for the same amino acid more than others, i.e., the frequency of one codon is higher than would be expected by chance. For example, leucine is specified by six different codons, some of which are rarely used. Codon frequency tables detailing genomic codon usage frequencies for most organisms are available. In recombinant gene technology, this effect is often utilized by performing a technique called codon optimization, where polynucleotides are designed using codons preferred by each host cell (e.g., human, hamster-derived cells, Escherichia coli cells, or Saccharomyces cerevisiae cells) to increase protein expression, for example. Therefore, it is assumed that the polynucleotide / nucleic acid molecules of this disclosure are codon-optimized. Nevertheless, polynucleotide / nucleic acid molecules encoding the constructs of the present invention may be designed using any codon encoding a desired amino acid.

[0252] According to one embodiment, the polynucleotide / nucleic acid molecule of the present invention encoding the polypeptide construct of the present invention is in the form of a single molecule or two or more distinct molecules. If the construct of the present invention is a single-chain construct, the polynucleotide / nucleic acid molecule encoding such a construct is most likely to also be in the form of a single molecule. However, it is also conceivable that different components of the polypeptide construct (e.g., different domains, e.g., a paratope (antigen-binding (epitope-binding) structure) containing a domain that binds to CLDN6, a paratope (antigen-binding (epitope-binding) structure) containing a domain that binds to CD3, and / or further domains such as an antibody constant domain) are located on separate polypeptide chains, in which case the polynucleotide / nucleic acid molecule is most likely to be in the form of two or more distinct molecules.

[0253] The same applies to vectors containing the polynucleotide / nucleic acid molecule of the present invention. If the construct of the present invention is a single-chain construct, one vector may contain the polynucleotide encoding the construct in one location (as an open reading frame, ORF). One vector may also contain two or more polynucleotide / nucleic acid molecules at separate locations (each having its own ORF), each of which encodes a different component of the construct of the present invention. A vector containing the polynucleotide / nucleic acid molecule of the present invention is envisioned to be in the form of a single vector or two or more separate vectors. In one embodiment, for the purpose of expressing the construct in a host cell, the host cell of the present invention should contain a polynucleotide / nucleic acid molecule encoding the construct, or a vector containing such polynucleotide / nucleic acid molecule as a whole, meaning that all components of the construct (whether encoded as a single molecule or at separate molecules / locations) assemble post-translation to form a biologically active construct of the present invention.

[0254] The present invention also provides vectors comprising the polynucleotide / nucleic acid molecule of the present invention. A vector is a nucleic acid molecule typically used as a vehicle for transferring (foreign) genetic material into a cell to ensure replication and / or expression of the genetic material. The term “vector” includes, but is not limited to, plasmids, viruses, cosmids, and artificial chromosomes. Some vectors are specifically designed for cloning (cloning vectors), while others are designed for protein expression (expression vectors). So-called transcription vectors are primarily used to amplify their inserts. DNA manipulation is typically performed on E. coli vectors that contain the elements necessary for their maintenance in E. coli. However, vectors may also have elements that allow them to be maintained in other organisms such as yeast, plant, or mammalian cells; these vectors are called shuttle vectors. Insertion of a vector into a target or host cell is typically called transformation for bacterial cells and transduction for eukaryotic cells, while insertion of a viral vector is often called transduction.

[0255] Generally, a manipulated vector contains an origin of replication, multiple cloning sites, and a selection marker. The vector itself is generally a nucleotide sequence, typically a DNA sequence, containing an insert (transgene) and a larger sequence that acts as the vector's "skeleton." The genetic code determines the polypeptide sequence of a given coding region, but other genomic regions can influence when and where these polypeptides are produced. Therefore, modern vectors may include additional features in addition to the transgene insert and skeleton, such as: promoters, genetic markers, antibiotic resistance, reporter genes, targeting sequences, and protein purification tags. Vectors called expression vectors (expression constructs) are specifically for the expression of a transgene in a target cell and generally contain regulatory sequences.

[0256] The term "regulatory sequence" refers to a DNA sequence necessary for the expression of a operably linked coding sequence in a particular host organism. For example, suitable regulatory sequences for prokaryotes include promoters, optional operator sequences, and ribosome binding sites. Eukaryotic cells are known to utilize promoters, polyadenylation signals, Kozak sequences, and enhancers.

[0257] Nucleic acids are "operably linked" when they are placed in a functional relationship with another nucleic acid sequence. For example, the DNA of a pre-sequence or secretion leader is operably linked to the DNA of a polypeptide if this DNA is expressed as a preprotein involved in the secretion of the polypeptide; a promoter or enhancer is operably linked to a coding sequence if this affects the transcription of the sequence; or a ribosome binding site is operably linked to a coding sequence if this ribosome binding site is positioned to facilitate translation. Generally, "operably linked" means that the linked nucleotide sequences are contiguous, and in the case of a secretion leader, contiguous and in the read phase. However, enhancers do not need to be contiguous. Linking is achieved by ligation at a convenient restriction site. If such a site does not exist, synthetic oligonucleotide adapters or linkers are used, according to conventional practice.

[0258] Transfection is the process of intentionally introducing nucleic acid molecules or polynucleotides (vectors are among the examples) into target cells. The term is primarily used for non-viral methods in eukaryotic cells. Transfection is often used to describe the viral transfer of nucleic acid molecules or polynucleotides. Transfection of animal cells typically involves creating transient pores or "holes" in the cell membrane to allow material uptake. Transfection can be carried out using biological particles (e.g., viral transfection, also called viral transfection), chemical-based methods (e.g., using calcium phosphate, lipofection, Fugene, cationic polymers, nanoparticles), or physical treatments (e.g., electroporation, microinjection, gene guns, cell squeezing, magnetofection, hydrostatic pressure, impulfection, sonication, phototransfection, heat shock).

[0259] The term "transformation" is used to describe the nonviral transfer of nucleic acid molecules or polynucleotides (including vectors) into bacteria and into non-animal eukaryotic cells, such as plant cells. Therefore, transformation is a genetic modification of a bacterial or non-animal eukaryotic cell resulting from the direct uptake from its periphery across the cell membrane and the subsequent integration of exogenous genetic material (nucleic acid molecules). Transformation can be achieved by artificial means. For transformation to occur, the cell or bacterium must be in a state of competence, which can occur as a time-limited response to environmental conditions such as starvation and cell density, and can also be artificially induced.

[0260] Furthermore, the present invention provides host cells transformed or transfused with the polynucleotide / nucleic acid molecule of the present invention or the vector of the present invention.

[0261] As used herein, the terms “host cell” or “recipient cell” are intended to include any individual cell or cell culture that can or has been a recipient of a vector, exogenous nucleic acid molecule and / or polynucleotide encoding a construct of the present invention; and / or a construct itself. The introduction of each substance into a cell is carried out by transformation, transfection and the like (see above). The term “host cell” is also intended to include a single-cell offspring or potential offspring. In subsequent generations, certain modifications may occur due to spontaneous, accidental, or intentional mutations, or due to environmental influences, so such offspring may not actually be completely identical to the parent cell (morphologically or in terms of genomic or total DNA complement), but are still included within the scope of the term as used herein. Suitable host cells include prokaryotic or eukaryotic cells, and include, but are not limited to, bacteria (e.g., Escherichia coli), yeast cells, fungal cells, plant cells, and animal cells (e.g., insect cells, and mammalian cells, e.g., hamster cells, mouse cells, rat cells, macaque cells, or human cells).

[0262] In addition to prokaryotes, eukaryotic microorganisms such as filamentous fungi or yeasts are suitable cloning or expression hosts for the constructs of the present invention. Saccharomyces cerevisiae, or common baker's yeast, are the most commonly used lower eukaryotic host microorganisms. However, many other genera, species, and strains are generally available and useful in the present invention, for example, Schizosaccharomyces pombe, K. lactis, K. fragilis (ATCC 12424), K. bulgaricus (ATCC 16045), K. wickeramii (ATCC 24178), K. waltii (ATCC 56500), K. drosophilarum (ATCC 16045) Hosts of the genus Kluyveromyces, such as K. thermotolerans and K. marxianus; yarrowia (European Patent No. 402226); Pichia pastoris (European Patent No. 183070); Candida; Trichoderma reesia (European Patent No. 244234); Neurospora crassa; Schwanniomyces occidentalis Hosts include the genus Schwanniomyces (such as Schwanniomyces occidentalis), as well as filamentous fungi such as Neurospora, Penicillium, Tolypocladium, and Aspergillus, such as A. nidulans and A. niger.

[0263] Host cells suitable for the expression of glycosylated constructs are derived from multicellular organisms. Examples of invertebrate cells include plant cells and insect cells. Numerous baculovirus strains and variants, as well as corresponding acceptable insect host cells derived from host organisms, have been identified (e.g., Spodoptera frugiperda (caterpillar), Aedes aegypti (mosquito), Aedes albopictus (mosquito), Drosophila melanogaster (fruit fly), and Bombyx mori (silkworm moth)). Various virus strains for translocation (e.g., the L-1 variant of Autographa californica NPV and the Bm-5 strain of Bombyx mori NPV) are publicly available, and such viruses may be used herein as viruses according to the present invention, and in particular may be used for translocation of armyworm (Spodoptera frugiperda) cells.

[0264] Plant cell cultures of cotton, maize, potato, soybean, petunia, tomato, Arabidopsis, and tobacco can also be used as hosts. Cloning and expression vectors useful for protein production in plant cell cultures are known to those skilled in the art. See, for example, Hiatt et al., Nature (1989) 342:76-78, Owen et al. (1992) Bio / Technology 10:790-794, Artsaenko et al. (1995) The Plant J 8:745-750, and Fecker et al. (1996) Plant Mol Biol 32:979-986.

[0265] However, the greatest interest has been in vertebrate cells, and the proliferation of vertebrate cells under culture conditions has become a routine procedure. Examples of useful mammalian host cell lines are listed below: SV40-transformed monkey kidney CV1 line (e.g., COS-7, ATCC CRL 1651); human embryonic kidney line (e.g., 293 cells or 293 cells subcloned for growth in suspension culture, Graham et al., J. GenVirol. 36:59 (1977)); baby hamster kidney cells (e.g., BHK, ATCC CCL 10); Chinese hamster ovary cells / -DHFR (e.g., CHO, Urlaub et al., Proc. Natl. Acad. Sci. USA 77:4216 (1980)); mouse Sertoli cells (e.g., TM4, Mather, Biol. Reprod. 23:243-251 (1980)); monkey kidney cells (e.g., CVI ATCC CCL 70); African green monkey kidney cells (e.g., VERO-76, ATCC CRL 1587); human cervical cancer cells (e.g., HELA, ATCC CCL 2); canine kidney cells (e.g., MDCK, ATCC CCL 34); buffalo rat liver cells (e.g., BRL 3A, ATCC CRL 1442); human lung cells (e.g., W138, ATCC CCL 75); human liver cells (e.g., Hep G2, 1413 8065); mouse mammary tumor cells (e.g., MMT 060562, ATCC CCL-51); TRI cells (Mather et al., Annals NY Acad.Sci. (1982) 383:44-68); MRC 5 cells; FS4 cells; and human hepatocellular carcinoma lineage (e.g., Hep G2).

[0266] In a further embodiment, the present invention provides a method for producing a construct of the present invention, the method comprising culturing host cells of the present invention under conditions that allow expression of the construct of the present invention, and recovering the produced construct from the culture.

[0267] As used herein, the term “culture” refers to the in vitro maintenance, differentiation, growth, proliferation, and / or propagation of cells under appropriate conditions in a culture medium. Cells are grown and maintained in cell growth medium at appropriate temperatures and gas mixtures. Culture conditions vary considerably depending on the cell type. Typical growth conditions are a temperature of approximately 37°C, a CO2 concentration of approximately 5%, and a humidity of approximately 95%. Growth medium recipes may differ, for example, in pH, the concentration of carbon sources (e.g., glucose), the nature and concentration of growth factors, and the presence of other nutrients (e.g., amino acids or vitamins). Growth factors used in supplemental media are often derived from animal blood serum (e.g., fetal bovine serum (FBS), calf serum (FCS), horse serum, and porcine serum). Cells can be grown in suspension or as adherent cultures. There are also cell lines that can grow to higher densities than adherent conditions because they have been modified to be viable in suspension culture.

[0268] The term “expression” includes, but is not limited to, any steps involved in the production of the construct of the present invention, including, transcription, post-transcriptional modification, translation, folding, post-translational modification, targeting to specific intracellular or extracellular locations, and secretion. The term “recover” refers to a series of processes intended to isolate a construct from a cell culture. The “recovery” or “purification” process can separate the protein and non-protein portions of a cell culture, ultimately separating the desired construct from all other polypeptides and proteins. The separation process typically utilizes differences in protein size, physicochemical properties, binding affinity, and biological activity. Preparative purification aims to produce relatively large quantities of purified protein for subsequent use, while analytical purification produces relatively small quantities of protein for various research or analytical purposes.

[0269] When recombinant technology is used, the construct can be produced intracellularly in the pericellular space or secreted directly into the culture medium. If the construct is produced intracellularly, the first step is to remove host cells or particulate fragments of the lysed fragment, for example, by centrifugation or ultrafiltration. The construct of the present invention can be produced in bacteria such as Escherichia coli (E. coli). After expression, the construct can be isolated from the bacterial cell paste in a soluble fraction and purified, for example, by affinity chromatography and / or size exclusion. Final purification can be carried out in a manner similar to that for purifying constructs expressed in mammalian cells and secreted into the culture medium. Carter et al. (Biotechnology (NY) 1992 Feb;10(2):163-7) describe a procedure for isolating antibodies secreted into the pericellular space of Escherichia coli (E. coli).

[0270] If the construct is secreted into the culture medium, the supernatant from such an expression system is generally first concentrated using a commercially available protein concentration filter, such as an ultrafiltration unit.

[0271] Constructions of the present invention prepared from host cells can be recovered or purified using, for example, hydroxyl apatite chromatography, gel electrophoresis, dialysis, and affinity chromatography. Other techniques for protein purification, such as fractionation in ion exchange columns, mixed-mode ion exchange, HIC, ethanol precipitation, size exclusion chromatography, reverse-phase HPLC, chromatography in silica, chromatography in heparin Sepharose, chromatography in anion or cation exchange resins (e.g., polyaspartate columns), immunoaffinity (protein A / G / L, etc.) chromatography, chromatofocusing, SDS-PAGE, ultracentrifugation, and ammonium sulfate precipitation, are also available depending on the construct to be recovered.

[0272] A protease inhibitor may be included in any of the aforementioned steps to inhibit protein degradation, and an antibiotic may be included to prevent the growth of contaminants.

[0273] Furthermore, the present invention provides a pharmaceutical composition or formulation comprising a construct of the present invention or a construct produced according to the process of the present invention.

[0274] As used herein, the term “pharmaceutical composition” refers to a composition suitable for administration to a patient, preferably a human patient. Particularly preferred pharmaceutical compositions of the present invention contain one or more constructs of the present invention, preferably in therapeutically effective amounts. Preferably, the pharmaceutical composition further comprises one or more suitable formulations of (pharmaceutically effective) carriers, stabilizers, excipients, diluents, solubilizers, surfactants, emulsifiers, preservatives, and / or adjuvants. The acceptable components of the composition are preferably nontoxic to the recipient at the doses and concentrations employed. Examples of pharmaceutical compositions of the present invention include, but are not limited to, liquid compositions, cryopreserved compositions, and lyophilized compositions.

[0275] The composition may contain a pharmaceutically acceptable carrier. Generally, as used herein, “pharmaceutically acceptable carrier” means all aqueous and non-aqueous solutions, sterile solutions, solvents, buffers, e.g., phosphate-buffered saline (PBS) solutions, water, suspensions, emulsions such as oil / water emulsions, various types of wetting agents, liposomes, dispersion media, and coatings that are suitable for pharmaceutical administration, and especially for parenteral administration. The use of such media and agents in pharmaceutical compositions is well known in the art, and compositions containing such carriers can be formulated by well known conventional methods.

[0276] Certain embodiments provide pharmaceutical compositions comprising the constructs of the present invention and one or more excipients, such as those described exemplary in this section and elsewhere in this specification. Excipients may be used for a variety of purposes (e.g., to adjust the physical, chemical, or biological properties of a formulation, e.g., viscosity), and / or in the processes of the present invention to improve efficacy and / or to stabilize such formulations and processes against degradation and deterioration caused by stress during, for example, manufacturing, shipping, storage, pre-preparation, administration, and thereafter. Excipients should generally be used at the lowest effective concentration.

[0277] In certain embodiments, the pharmaceutical composition may include formulation materials for modifying, maintaining, or preserving specific properties of the composition, such as pH, molar osmotic pressure, viscosity, clarity, color, isotonicity, odor, sterility, stability, dissolution rate or release rate, adsorption or osmosis (see Remington's Pharmaceutical Sciences, 18th Edition, 1990, Mack Publishing Company). Suitable formulation materials in such embodiments may, but are not limited to, the following: ·amino acid • Antimicrobial agents such as antibacterial agents and antifungal agents • Antioxidants Buffers, buffer systems, and buffering agents used to maintain a composition at or slightly below physiological pH, typically within the range of about 5 to about 8 or 9. • Non-aqueous solvents, vegetable oils, and organic esters for injection Aqueous carriers include water, alcohol / aqueous solutions, emulsions, or suspensions (physiological saline and buffer media are examples). • Biodegradable polymers such as polyester • Volume expander Chelatives • Isotonic agents and absorption retarders • Complexing agent • Filler ·carbohydrates Preferably, a human-derived (low molecular weight) protein, polypeptide, or protein carrier. • Colorants and flavorings • Sulfur-containing reducing agent • Diluent ·emulsifier • Hydrophilic polymer • Salt-forming counterions • Preservatives • Metal complex • Solvents and co-solvents • Sugars and sugar alcohols • Suspension • Surfactants or bluing agents • Stabilizer • Isotonic accelerator • Parenteral delivery media • Intravenous delivery medium.

[0278] It is common knowledge that various components of a pharmaceutical composition can have different effects. For example, amino acids can act as buffers, stabilizers, and / or antioxidants; mannitol can act as a volume extender and / or isotonic enhancer; and sodium chloride can act as a delivery medium and / or isotonic enhancer.

[0279] In relation to the present invention, the pharmaceutical composition is (a) Structures described herein, (b) at least one type of buffer, (c) at least one type of sugar, and (d) at least one surfactant Includes, The pH of the pharmaceutical composition is in the range of 3.5 to 6.

[0280] In the above-described composition, the first domain preferably has an isoelectric point (pI) in the range of 4 to 9.5, the second domain has a pI in the range of 8 to 10, preferably 8.5 to 9.0, and the construct optionally includes a third domain containing two polypeptide monomers, each containing a hinge, a CH2 domain and a CH3 domain, the two polypeptide monomers fused to each other via a peptide linker.

[0281] In the above composition, it is further assumed that at least one buffer is present in a concentration range of 5 to 200 mM, more preferably in a concentration range of 10 to 50 mM. It is also assumed that at least one sugar is selected from the group consisting of monosaccharides, disaccharides, cyclic polysaccharides, sugar alcohols, linear branched dextran, or linear unbranched dextran. The disaccharide is also assumed to be selected from the group consisting of sucrose, trehalose, mannitol, sorbitol, and combinations thereof. It is further assumed that the sugar alcohol is sorbitol. It is also assumed that at least one sugar is present in a concentration range of 1 to 15% (m / V), preferably in a concentration range of 9 to 12% (m / V). It is further assumed that the construct is present in a concentration range of 0.1 to 8 mg / ml, preferably 0.2 to 2.5 mg / ml, more preferably 0.25 to 1.0 mg / ml.

[0282] According to one embodiment of the above composition, at least one surfactant is selected from the group consisting of polysorbate 20, polysorbate 40, polysorbate 60, polysorbate 80, poloxamer 188, Pluronic F68, Triton X-100, polyoxyethylene, PEG3350, PEG4000, and combinations thereof. It is further assumed that at least one surfactant is present at a concentration in the range of 0.004 to 0.5% (m / V), preferably in the range of 0.001 to 0.01% (m / V). The pH of the composition is assumed to be in the range of 4.0 to 5.0, preferably in the range of 4.2. The pharmaceutical composition is also assumed to have a molar osmotic pressure concentration in the range of 150 to 500 mOsm. The pharmaceutical composition is further assumed to contain excipients selected from the group consisting of one or more polyols and one or more amino acids. In relation to the present invention, it is assumed that one or more excipients are present at a concentration in the range of 0.1 to 15% (w / V).

[0283] The present invention also provides a pharmaceutical composition comprising (a) a construct described herein in a concentration range of preferably 0.1 to 8 mg / ml, preferably 0.2 to 2.5 mg / ml, more preferably 0.25 to 1.0 mg / ml; (b) 10 mM glutamate or acetate; (c) 9% (m / V) sucrose or 6% (m / V) sucrose and 6% (m / V) hydroxypropyl-β-cyclodextrin; and (d) 0.01% (m / V) polysorbate 80, wherein the pH of the liquid pharmaceutical composition is 4.2.

[0284] The compositions of the present invention are expected to include, in addition to the constructs of the present invention as defined herein, further biologically active agents depending on the intended use of the composition. Such agents may be drugs acting on the gastrointestinal system, drugs acting as cell proliferation inhibitors, drugs preventing hyperuricemia, drugs suppressing immune responses, drugs modulating inflammatory responses, drugs acting on the circulatory system, and / or cytokines known in the art. Furthermore, the polypeptide constructs of the present invention are also expected to be used in combination therapy, i.e., in combination with other anticancer drugs.

[0285] In this regard, the pharmaceutical composition of the present invention (which includes a construct comprising a domain that binds to CLDN6 on the surface of a target cell and another domain that binds to CD3 on the surface of a T cell, as described more specifically above herein) is envisioned to further include an agent, preferably an antibody or construct, that binds to a protein of the immune checkpoint pathway (such as PD-1 or CTLA-4) or a co-stimulatory immune checkpoint receptor (such as 4-1BB). The present invention also refers to a combination of a polypeptide construct according to the present invention (which includes a polypeptide construct comprising a domain comprising a paratope (antigen-binding (epitope-binding) structure) that binds to CLDN6 on the surface of a target cell and another domain comprising a paratope (antigen-binding (epitope-binding) structure) that binds to CD3 on the surface of a T cell) and an active agent, preferably an antibody or polypeptide construct, that binds to a protein of the immune checkpoint pathway (such as PD-1 or CTLA-4) or a co-stimulatory immune checkpoint receptor (such as 4-1BB). Due to the properties of at least two components of the combination, i.e., their pharmaceutically active properties, the combination may also be called a therapeutic combination. In some embodiments, the combination may be in the form of a pharmaceutical composition or a kit. According to one embodiment, the pharmaceutical composition or combination comprises the construct of the present invention and an antibody or construct that binds to PD-1. Anti-PD-1 binding proteins useful for this purpose are described in detail, for example, in International Publication PCT / US2019 / 013205, which is incorporated herein by reference.

[0286] In certain embodiments, the optimal pharmaceutical composition is determined, for example, by the intended route of administration, the delivery format, and the desired dosage. See, for example, Remington's Pharmaceutical Sciences. In certain embodiments, such a composition may affect the ...

Claims

1. A polypeptide or polypeptide construct comprising a domain that binds to CLDN6, wherein the domain comprises a VH region comprising CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and a VL region comprising CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO:

18.

2. A polypeptide or polypeptide construct comprising a domain that binds to CLDN6, wherein the domain comprises a VH region having the amino acid sequence shown in SEQ ID NO: 11 and a VL region having the amino acid sequence shown in SEQ ID NO:

12.

3. A polypeptide or polypeptide construct that binds to CLDN6, comprising the amino acid sequence shown in SEQ ID NO:

19.

4. A polypeptide or polypeptide construct that binds to CLDN6, comprising the amino acid sequence shown in SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, or SEQ ID NO:

24.

5. A polypeptide or polypeptide construct comprising a domain that binds to human CLDN6 (SEQ ID NO: 1), a domain that binds to human CD3, and a domain that extends the half-life of the polypeptide, wherein the domain that binds to CLDN6 comprises a VH region including CDR-H1 shown in SEQ ID NO: 13, CDR-H2 shown in SEQ ID NO: 14, and CDR-H3 shown in SEQ ID NO: 15, and a VL region including CDR-L1 shown in SEQ ID NO: 16, CDR-L2 shown in SEQ ID NO: 17, and CDR-L3 shown in SEQ ID NO:

18.

6. The polypeptide or polypeptide construct according to claim 5, wherein the domain that binds to CLDN6 includes a VH region having the amino acid sequence shown in SEQ ID NO: 11 and a VL region having the amino acid sequence shown in SEQ ID NO:

12.

7. A polypeptide or polypeptide construct according to claim 5 or 6, comprising the amino acid sequence shown in SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, or SEQ ID NO:

24.

8. A polypeptide or polypeptide construct according to any one of claims 5 to 7, which, when the domain that binds to CLDN6 is determined by an in vitro assay using cells expressing a variant of wild-type CLDN6 shown in SEQ ID NO: 1, comprising at least one or more of the following mutations M29X, R145X, and / or Q156X, induces cytotoxicity that is at least 100-fold, at least 250-fold, and at least 500-fold lower than the cytotoxicity measured by an in vitro assay using cells expressing CLDN6 shown in SEQ ID NO:

1.

9. The polypeptide or polypeptide construct according to any one of claims 1 to 8, wherein the construct is a single-chain construct.

10. The half-life extension domain, which contains two polypeptide monomers, comprises a hinge, a CH2 domain, and a CH3 domain, in the order of amino to carboxyl. Hinge - CH2 - CH3 - Linker - Hinge - CH2 - CH3 A polypeptide or polypeptide construct according to any one of claims 5 to 9, comprising:

11. The polypeptide or polypeptide construct according to claim 10, wherein the CH2 domain includes an intradomain cysteine ​​disulfide crosslink.

12. (i) The antigen-binding (epitope-binding) domain that binds to CLDN6 contains two antibody-variable domains, and the antigen-binding (epitope-binding) domain that binds to CD3 contains two antibody-variable domains; (ii) The antigen-binding (epitope-binding) domain that binds to CLDN6 contains one antibody-variable domain, and the antigen-binding (epitope-binding) domain that binds to CD3 contains two antibody-variable domains; (iii) The antigen-binding (epitope-binding) domain that binds to CLDN6 contains two antibody-variable domains, and the antigen-binding (epitope-binding) domain that binds to CD3 contains one antibody-variable domain; or (iv) The antigen-binding (epitope-binding) domain that binds to CLDN6 contains one antibody-variable domain, and the antigen-binding (epitope-binding) domain that binds to CD3 contains one antibody-variable domain, A polypeptide or polypeptide construct according to any one of claims 1 to 11.

13. The polypeptide or polypeptide construct according to claim 12, wherein the antigen-binding (epitope-binding) domain that binds to CLDN6 and the antigen-binding (epitope-binding) domain that binds to CD3 are fused to another domain via a peptide linker.

14. The polypeptide or polypeptide construct is arranged in the order of amino to carboxyl, or carboxyl to amino: (a) Antigen-binding (epitope-binding) domain that binds to CLDN6; (b) Peptide linker; (c) Antigen-binding (epitope-binding) domain that binds to CD3 A polypeptide or polypeptide construct according to any one of claims 1 to 13, comprising:

15. The polypeptide or polypeptide construct is arranged in the order of amino to carboxyl, or in the order of carboxyl to amino. (a) A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs: 563 to 575; (b) The first polypeptide monomer of the third domain; (c) A peptide linker having an amino acid sequence selected from the group consisting of SEQ ID NOs: 563 to 575; and (d) The second polypeptide monomer of the third domain The polypeptide or polypeptide construct according to claim 14, further comprising, wherein the third domain has the amino acid sequence shown in SEQ ID NOs. 581 to 637.

16. A polypeptide or polypeptide construct according to any one of claims 1 to 15, comprising a domain that binds to CD3, comprising a VH domain containing the CDR H1 to H3 sequences shown in SEQ ID NOs. 670, 671, and 672, and a VL domain containing the CDR L1 to L3 sequences shown in SEQ ID NOs. 673, 674, and 675.

17. A polypeptide or polypeptide construct according to any one of claims 1 to 16, comprising a domain that binds to CD3, including the VH domain shown in Sequence ID No. 676 and the VL domain shown in Sequence ID No.

677.

18. A polypeptide or polypeptide construct according to any one of claims 1 to 17, comprising a domain that binds to CD3, including the scFv domain shown in Sequence ID No.

678.

19. A polynucleotide encoding a polypeptide or polypeptide construct according to any one of claims 1 to 18.

20. A vector comprising the polynucleotide described in claim 19.

21. A host cell transformed or transfected with the polynucleotide described in claim 19 or the vector described in claim 20.

22. A method for producing a polypeptide or polypeptide construct according to any one of claims 1 to 18, comprising culturing the host cells according to claim 21 under conditions that enable the expression of the polypeptide or polypeptide construct, and recovering the polypeptide or polypeptide construct from the culture.

23. A pharmaceutical composition comprising a polypeptide or polypeptide construct according to any one of claims 1 to 18.

24. A pharmaceutical composition comprising a polypeptide or polypeptide construct according to any one of claims 1 to 18, for use in the prevention, treatment, or remission of neoplasms.

25. A pharmaceutical composition comprising a polypeptide or polypeptide construct according to any one of claims 1 to 18 for the prevention, treatment or remission of a disease, wherein the disease is selected from the group consisting of lung cancer including germ cell carcinoma, ovarian cancer, uterine cancer, small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), and pediatric neoplasms selected from Wilms' tumor, extracranial rhabdoid or fibrinogenic small round cell tumor.

26. The pharmaceutical composition according to claim 25, wherein the lung cancer is non-small cell lung cancer (NSCLC).

27. A kit comprising a polypeptide or polypeptide construct according to any one of claims 1 to 18, a polynucleotide according to claim 19, a vector according to claim 20, and / or a host cell according to claim 21.

28. A pharmaceutical composition comprising a polypeptide or polypeptide construct according to any one of claims 1 to 18 for treating or improving a proliferative disorder, neoplastic disorder, cancer or immunological disorder, wherein the disorder is selected from the group consisting of germ cell carcinoma, ovarian cancer, uterine cancer, lung cancer including small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), and pediatric neoplasms selected from Wilms' tumor, extracranial rhabdoid or fibrous round cell tumor.

Images