antigen-binding molecules

Abstract

The present invention relates to a pair of binding molecules comprising complementary portions of effector domains, which can form functional effector domains when bound to their target antigens on the surface of a cell. Specifically, the present invention relates to a pair of binding molecules in which the complementary portions of the effector domains are complemented with inactive complementary domains, but no functional effector domains are formed, providing the binding molecules with advantageous properties such as productivity, stability, and / or biological functionality.

Description

[Technical Field]

[0001] FIELD OF THE INVENTION The present invention relates to a pair of binding molecules comprising complementary portions of effector domains, which can form functional effector domains when bound to their target antigens on the surface of a cell. Specifically, the present invention relates to a pair of binding molecules in which the complementary portions of the effector domains are complemented with inactive complementary domains, but no functional effector domains are formed, providing the binding molecules with advantageous properties such as productivity, stability, and / or biological functionality. [Background technology]

[0002] background T cell engagers, or T cell bispecific antibodies (TCBs), are bispecific antibodies that recognize target cell antigens, such as tumor antigens expressed on tumor cells, in one binding moiety and T cell receptors in the other. TCBs are highly promising cancer immunotherapies. Cross-linking of CD3 with target cell antigens triggers T cell activation, proliferation, and cytokine release, leading to target cell death (Bacac et al., Clin Cancer Res (2016) 22, 3286-97; Bacac et al., Oncoimmunology (2016) 5, e1203498).

[0003] However, despite the efficacy of T cell redirection approaches, TCB treatment can be associated with safety disadvantages due to on-target off-tumor cytotoxicity and cytokine release. Particularly in the treatment of solid tumors, on-target off-tumor activity remains a challenge to realize the full potential of T cell bispecific antibodies.

[0004] Clinical experience with T cell bispecific antibodies has so far shown that high rates of durable responses are achievable in hematological malignancies, but remains very limited in solid tumors. Various T cell engagers have been terminated in phase I trials. While the reasons for terminating these trials may vary, multiple trials have demonstrated adverse events, often accompanied by CRS despite prophylactic corticosteroid treatment, and limited positive pharmacodynamic signals at fairly low doses.

[0005] The limited success of T cell bispecific antibodies, particularly in the treatment of solid tumors, is due to the lack of targets in solid tumors that are tumor-specific or expressed only on physiological tissues considered nonessential (e.g., CD19 or CD20 on B cells). Conventional T cell bispecific antibodies for solid tumors have had limited efficacy due to a narrow therapeutic window resulting from on-target, off-tumor activation of T cells. For example, clinical trials using catumaxomab for the treatment of solid tumors have demonstrated dose-limiting toxicity (Mau-Sorensen et al. (2015) Cancer Chemother Pharmacol 75, 1065-1073; Borlak et al. (2016) Oncotarget 7, 28059-28074). Indeed, on-target, off-tumor activation of T cell engagers has long been a challenge due to the lack of efficacy and truly tumor-specific targets for such therapeutic modalities.

[0006] Therefore, the development of drugs with tumor-restricting activity, such as T cell bispecific antibodies, is needed to increase the therapeutic index and improve patient outcomes.

[0007] Although achieving this requires novel approaches and is technically challenging, generating inactive prodrugs that are primarily or solely active within the tumor microenvironment is an area of ​​intensive research.

[0008] To mitigate the systemic toxicity often seen with T cell bispecific antibodies, for example, Stuhler and colleagues have disclosed a "split" approach for the on-target in situ generation of CD3 binders commonly used in this compound class (Banaszek et al. (2019) Nature Comm 10, 5387; PCT Publication No. 2013 / 104804). According to this concept, the functional antibody-binding fragment (Fv) of a CD3 binder is split into a VL domain and a VH domain, neither of which is CD3-binding competent as individual domains, and both V domains are separately contained in separate prodrug molecules, i.e., a CD3-VH prodrug and a CD3-VL prodrug.

[0009] However, VL and VH domains as separate domains are generally less stable than assembled Fv fragments, and expressibility is often limited because the VH domain tends to stabilize the VL domain, while the VL domain can enhance the folding of the VH domain (Ewert et al. (2003) J Molecular Biol 325, 531-553). Furthermore, isolated V domains exhibit hydrophobic surface patches at the interface with their cognate V domains, making them prone to aggregation as separate domains, especially under long-term storage or stress conditions such as elevated temperatures. Many CD3 binders frequently used in the industry for T cell bispecific antibodies indeed suffer from these limitations.

[0010] Thus, there remains a need for improved "split" approaches that can be applied to, for example, T cell bispecific antibodies. Summary of the Invention

[0011] Summary of the Invention The present invention relates to pairs of binding molecules comprising complementary portions of effector domains, such binding molecules being capable of forming functional effector domains when bound to their target antigens on the surface of a cell.

[0012] The inventors have found that complementing the complementary portion of an effector domain with an inactive complementarity domain, while a functional effector domain is not formed, provides advantageous properties to the binding molecule, including improved productivity (e.g., increased production yield, easier purification), stability (including after exposure to stress conditions), and / or biological functionality (e.g., reduced aggregation in the absence of cells expressing the binding molecule's target antigen).

[0013] The complementarity domain covers the (potentially hydrophobic) interface between portions of the effector domain, aiding in the folding and stability of the binding molecule. Furthermore, the complementarity domain can serve as a modulator of the association equilibrium of the binding molecule. In uncomplemented binding molecules, the assembly equilibrium depends on the local concentration of the binding molecule and the association rate constant of the effector domain portion. In the complementarity approach described herein, assembly further depends on the dissociation rate constants of the effector domain and their respective complementary domain portions. Thus, in complemented binding molecules, their assembly equilibrium shifts to higher concentrations, resulting in, for example, unfavorable target-independent assembly in the circulation and favorable target-dependent assembly on target cells. Adjusting the therapeutic window is possible by fine-tuning the interaction between the effector domain portion and the complementary domain.

[0014] Thus, in a first aspect, the present invention provides a method for producing a medicament for the treatment of a pulmonary arthritis, comprising: (a) a first binding molecule comprising (i) a first antigen-binding domain capable of binding to a target antigen, (ii) a first portion of an effector domain, and (iii) a first complementarity domain capable of binding to the first portion of the effector domain; and (b) a binding molecule pair comprising (i) a second antigen-binding domain capable of binding to a target antigen, (ii) a second portion of an effector domain, and (iii) a second binding molecule comprising a second complementarity domain capable of binding to said second portion of said effector domain, the first and second portions of the effector domain can bind to each other to form a functional effector domain when the first antigen-binding domain and the second antigen-binding domain bind to a target antigen on a cell surface; The first complementarity domain and the second complementarity domain are bound to the first and second portions of the effector domain, respectively, and the first and second portions of the effector domain are not bound to each other, providing a binding molecule pair.

[0015] In another aspect, the present invention provides a binding molecule that forms part of a binding molecule pair of the present invention.

[0016] According to a further aspect of the present invention, there are provided isolated polynucleotides encoding the binding molecule pairs or binding molecules of the invention, and host cells comprising the isolated polynucleotides of the invention. In another aspect, there is provided a method of producing a binding molecule pair, comprising the steps of (a) culturing a host cell of the invention under conditions suitable for expression of the binding molecule pair, and optionally (b) recovering the binding molecule pair.

[0017] The present invention further provides pharmaceutical compositions comprising a binding molecule or binding molecule pair of the invention and a pharmaceutically acceptable carrier.

[0018] The present invention also encompasses methods of using the binding molecules, binding molecule pairs, and pharmaceutical compositions of the invention. In one aspect, the present invention provides a binding molecule pair, binding molecule, or pharmaceutical composition according to the invention for use as a medicament. In one aspect, the present invention provides a binding molecule pair, binding molecule, or pharmaceutical composition according to the invention for use in treating a disease. Also provided is the use of a binding molecule pair, binding molecule, or pharmaceutical composition according to the invention in the manufacture of a medicament, and the use of a binding molecule pair, binding molecule, or pharmaceutical composition according to the invention in the manufacture of a medicament for treating a disease. The present invention also provides a method of treating a disease in an individual, comprising administering to the individual an effective amount of a binding molecule pair according to the invention. DETAILED DESCRIPTION OF THE INVENTION

[0019] Description of the Invention definition Terms are used herein as commonly used in the art unless otherwise defined herein.

[0020] As used herein, the terms "first," "second," or "third," with respect to antigen-binding domains and the like, are used for convenience in distinguishing between cases where more than one of each type of moiety is present. The use of these terms is not intended to confer a particular order or orientation of the moieties unless explicitly stated.

[0021] As used herein, the term "binding molecule" refers to a polypeptide molecule (composed of one or more polypeptide chains) that can bind to an antigen. Binding molecules can be derived from antibodies and typically contain an antigen-binding domain.

[0022] The term "antibody" is used herein in the broadest sense and encompasses a variety of antibody structures, including, but not limited to, monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies), and antibody fragments, so long as they exhibit the desired antigen-binding activity.

[0023] "Antibody fragment" refers to a molecule other than an intact antibody that contains a portion of an intact antibody that binds to the antigen to which the intact antibody binds. Examples of antibody fragments include, but are not limited to, Fv, Fab, Fab', Fab'-SH, F(ab')2; diabodies; linear antibodies; single-chain antibody molecules (e.g., scFv and scFab); single-domain antibodies; and multispecific antibodies formed from antibody fragments. For a review of specific antibody fragments, see Hollinger and Hudson, Nature Biotechnology 23:1126-1136 (2005).

[0024] The terms "full-length antibody," "intact antibody," and "whole antibody" are used interchangeably herein to refer to an antibody having a structure substantially similar to a native antibody structure.

[0025] An "antigen-binding domain" is a molecular domain capable of binding to an antigen. This term particularly refers to the antigen-binding domain of an antibody, i.e., a portion of an antibody comprising the region that binds to and is complementary to part or all of the antigen. Thus, in certain embodiments, the antigen-binding domain herein is the antigen-binding domain of an antibody. Such an antigen-binding domain may be provided, for example, by one or more antibody variable domains (also referred to as antibody variable regions). Thus, in certain embodiments, the antigen-binding domain herein comprises an antibody light chain variable domain (VL) and an antibody heavy chain variable domain (VH). The antigen-binding domain may also be provided by a non-antibody-derived molecule, such as ankyrin repeat proteins or lipocalin-derived binding molecules (DARPins®, Anticalins®).

[0026] The term "variable region" or "variable domain" refers to the domain of an antibody heavy chain or light chain that is involved in binding the antibody to an antigen. The variable domains of the heavy and light chains of natural antibodies (VH and VL, respectively) generally have similar structures, and each domain contains four conserved framework regions (FR) and complementarity-determining regions (CDR). See, for example, Kindt et al., Kuby Immunology, Vol. 6, No. 1, pp. 111-114, 2003. 版, W.H. Freeman & Co., page 91 (2007). A single VH or VL domain may be sufficient to confer antigen-binding specificity. Furthermore, antibodies that bind to a specific antigen can be isolated using the VH or VL domain of an antibody that binds to that antigen and screening libraries of complementary VL or VH domains, respectively. See, e.g., Portolano et al. J. Immunol. 150:880-887, 1993; Clarkson et al. Nature 352:624-628, 1991. When used herein in reference to variable region sequences, "Kabat numbering" refers to the numbering system set forth by Kabat et al., Sequences of Proteins of Immunological Interest, 5th ed. Public Health Service, National Institutes of Health, Bethesda, MD (1991).

[0027] As used herein, the amino acid positions of all heavy and light chain constant regions and domains are numbered according to the Kabat numbering system as described in Kabat, et al., Sequences of Proteins of Immunological Interest, 5th ed., Public Health Service, National Institutes of Health, Bethesda, MD (1991), and is referred to herein as "Kabat numbering" or "Kabat numbering." Specifically, the Kabat numbering system (see Kabat et al., Sequences of Proteins of Immunological Interest, 5th ed., Public Health Service, National Institutes of Health, Bethesda, MD (1991) pp. 647-660) is used for the light chain constant domains CL of the kappa and lambda isotypes, and the Kabat EU index numbering system (see pp. 661-723) is used for the heavy chain constant domains (CH1, hinge, CH2 and CH3), which is further clarified herein by reference in this case to "numbering according to the Kabat EU index" or "Kabat EU index numbering."

[0028] As used herein, the term "hypervariable region" or "HVR" refers to each region of an antibody variable domain whose sequence is hypervariable and which determines antigen-binding specificity, e.g., a "complementarity-determining region" ("CDR"). Typically, antibodies contain six CDRs; three in the VH (HCDR1, HCDR2, HCDR3) and three in the VL (LCDR1, LCDR2, LCDR3). Exemplary CDRs herein include the following: (a) hypervariable loops occurring at amino acid residues 26-32 (L1), 50-52 (L2), 91-96 (L3), 26-32 (H1), 53-55 (H2), and 96-101 (H3) (Chothia and Lesk, J. Mol. Biol. 196:901-917 (1987)); (b) CDRs occurring at amino acid residues 24-34 (L1), 50-56 (L2), 89-97 (L3), 31-35b (H1), 50-65 (H2), and 95-102 (H3) (Kabat et al., Sequences of Proteins of Immunological Interest, 5th ed. Public Health Service, National Institutes of Health, Bethesda, MD (1991)); and (c) Antigen contact sites located at amino acid residues 27c-36 (L1), 46-55 (L2), 89-96 (L3), 30-35b (H1), 47-58 (H2), and 93-101 (H3) (MacCallum et al. J. Mol. Biol. 262:732-745 (1996)).

[0029] Unless otherwise indicated, CDRs are determined according to Kabat et al., supra. Those skilled in the art will understand that CDR designations may be determined according to Chothia, supra, McCallum, supra, or any other scientifically accepted nomenclature system.

[0030] "Framework" or "FR" refers to variable domain residues other than the complementarity-determining regions (CDRs). The FR of a variable domain generally consists of four FR domains: FR1, FR2, FR3, and FR4. Thus, the HVR and FR sequences generally appear in the following order in VH (or VL): FR1-HCDR1 (LCDR1)-FR2-HCDR2 (LCDR2)-FR3-HCDR3 (LCDR3)-FR4.

[0031] Unless otherwise indicated, CDR residues and other residues in the variable domain (eg, FR residues) are numbered herein according to Kabat et al., supra.

[0032] The term "immunoglobulin molecule" as used herein refers to a protein having the structure of a naturally occurring antibody. For example, IgG class immunoglobulins are heterotetrameric glycoproteins of about 150,000 daltons, consisting of two disulfide-bonded light chains and two heavy chains. From the N-terminus to the C-terminus, each heavy chain has a variable domain (VH) (also called variable heavy chain domain or heavy chain variable region), followed by three constant domains (CH1, CH2 and CH3) (also called heavy chain constant region). Similarly, from N- to C-terminus, each light chain has a variable domain (VL (also called variable light domain or light chain variable region)) followed by a constant light (CL) domain (also called light chain constant region). Immunoglobulin heavy chains may be assigned to one of five types, called α (IgA), δ (IgD), ε (IgE), γ (IgG), or μ (IgM), some of which may be further divided into subtypes, e.g., γ1 (IgG1), γ2 (IgG2), γ3 (IgG3), γ4 (IgG4), α1 (IgA1), and α2 (IgA2). Immunoglobulin light chains may be assigned to one of two types, called kappa (κ) and lambda (λ), based on the amino acid sequence of their constant domain. Immunoglobulins essentially consist of two Fab molecules and an Fc domain, connected via an immunoglobulin hinge region.

[0033] The "class" of an antibody or immunoglobulin refers to the type of constant domain or constant region possessed by the antibody or immunoglobulin heavy chain. There are five major classes of antibodies: IgA, IgD, IgE, IgG, and IgM, some of which can be further divided into subclasses (isotypes), e.g., IgG1, IgG2, IgG3, IgG4, IgA1, and IgA2. The heavy chain constant domains corresponding to the different classes of immunoglobulins are called α, δ, ε, γ, and μ, respectively.

[0034] A "Fab molecule" refers to a protein consisting of the VH and CH1 domains of an immunoglobulin heavy chain (a "Fab heavy chain") and the VL and CL domains of a light chain (a "Fab light chain").

[0035] The term "multispecific" means that a binding molecule (e.g., an antibody) can specifically bind to at least two different antigenic determinants. A multispecific binding molecule (e.g., an antibody) can be, for example, a bispecific binding molecule. Typically, a bispecific binding molecule contains two antigen-binding sites, each specific for a different antigenic determinant. In certain embodiments, a multispecific (e.g., bispecific) binding molecule can simultaneously bind to two antigenic determinants, particularly two antigenic determinants expressed on the same cell, adjacent cells, or cells within the same tissue.

[0036] As used herein, the term "valency" refers to the presence of a specific number of antigen-binding sites in a binding molecule. Thus, the term "monovalent binding to an antigen" indicates the presence of one (and no more than one) antigen-binding site specific for an antigen in the binding molecule.

[0037] "Antigen-binding site" refers to the site of a binding molecule, i.e., one or more amino acid residues, that provides interaction with an antigen. For example, the antigen-binding site of an antibody comprises amino acid residues from the complementarity-determining regions (CDRs). A naturally occurring immunoglobulin molecule typically contains two antigen-binding sites, and a Fab molecule typically has one antigen-binding site.

[0038] As used herein, the term "antigenic determinant" or "antigen" refers to a site (e.g., a contiguous stretch of amino acids or a three-dimensional structure composed of different regions of non-contiguous amino acids) on a polypeptide macromolecule to which an antigen-binding domain binds to form an antigen-binding domain-antigen complex. Useful antigenic determinants may be found, for example, on the surface of tumor cells, on the surface of virally infected cells, on the surface of other diseased cells, on the surface of immune cells, free in serum, and / or in the extracellular matrix (ECM). In certain embodiments, the antigen is a human protein.

[0039] By "T cell antigen" is meant an antigenic determinant expressed on the surface of a T lymphocyte.

[0040] As used herein, "activating T cell antigen" refers to an antigenic determinant expressed on the surface of T lymphocytes, particularly cytotoxic T lymphocytes, which can induce T cell activation upon interaction with an antigen-binding molecule. Specifically, the interaction of an antigen-binding molecule with an activating T cell antigen can induce T cell activation by triggering a signal transduction cascade of the T cell receptor complex. In a specific embodiment, the activating T cell antigen is CD3, particularly the epsilon subunit of CD3.

[0041] As used herein, "T cell activation" refers to one or more cellular responses of T lymphocytes, particularly cytotoxic T lymphocytes, selected from proliferation, differentiation, cytokine secretion, release of cytotoxic effector molecules, cytotoxic activity, and expression of activation markers. Suitable assays for measuring T cell activation are known in the art and are described herein.

[0042] Unless otherwise specified, "CD3" refers to any native CD3 from any vertebrate source, including mammals such as primates (e.g., humans), non-human primates (e.g., cynomolgus monkeys), and rodents (e.g., mice and rats). The term encompasses "full-length," unprocessed CD3, as well as any form of CD3 resulting from intracellular processing. The term also encompasses naturally occurring variants of CD3, such as splice variants or allelic variants. In one embodiment, the CD3 is human CD3, particularly the epsilon subunit of human CD3 (CD3ε). The amino acid sequence of human CD3ε is set forth in SEQ ID NO: 57 (without the signal peptide). See also UniProt (www.uniprot.org) entry number P07766 (version 209), or NCBI (www.ncbi.nlm.nih.gov / ) RefSeq NP_000724.1. In another embodiment, the CD3 is cynomolgus monkey (Macaca fascicularis) CD3, particularly cynomolgus monkey CD3ε. The amino acid sequence of cynomolgus monkey CD3ε is shown in SEQ ID NO: 58 (without signal peptide). See also NCBI GenBank No. BAB71849.1. In a specific embodiment, the binding molecule of the present invention binds to an epitope of CD3 that is conserved between CD3 antigens from different species, particularly human and cynomolgus monkey CD3. In a specific embodiment, the binding molecule binds to human CD3.

[0043] As used herein, "target antigen" refers to an antigenic determinant presented on the surface of a target cell, e.g., a cell in a tumor, such as a cancer cell, or a cell in the tumor stroma (in this case, a "tumor antigen"). Preferably, the target antigen is not CD3 and / or is expressed on a different cell than CD3.

[0044] "HER2" (also known as erbB-2 or CD340), unless otherwise specified, refers to any naturally occurring HER2 of any vertebrate origin, including mammals such as primates (e.g., humans), non-human primates (e.g., cynomolgus monkeys), and rodents (e.g., mice and rats). The term encompasses unprocessed "full-length" HER2, as well as any form of HER2 resulting from intracellular processing. The term also encompasses naturally occurring variants of HER2, such as splice variants or allelic variants. In one embodiment, the HER2 is human HER2. The amino acid sequence of human HER2 is set forth in UniProt (www.uniprot.org) entry number Q9UK79 (version 95).

[0045] The terms "anti-[protein x] (e.g., CD3) antibody" and "antibody that binds [protein x] (e.g., CD3)" refer to an antibody that can bind [protein x] (e.g., CD3) with sufficiently high affinity to be useful as a diagnostic and / or therapeutic agent targeting [protein x] (e.g., CD3). In one embodiment, the extent of binding of an anti-[protein x] (e.g., CD3) antibody to an unrelated, non-[protein x] (e.g., CD3) protein is less than about 10% of the binding of the antibody to [protein x] (e.g., CD3), as measured, for example, by surface plasmon resonance (SPR). In certain embodiments, an antibody that binds to [protein x] (e.g., CD3) has a dissociation constant (K D ) is 1 μM or less, 500 nM or less, 200 nM or less, or 100 nM or less. The antibody has a K of 1 μM or less, as measured, for example, by SPR. D An anti-[protein x] (e.g., CD3) antibody is said to "specifically bind" to [protein x] (e.g., CD3) if it has the following epitope: In certain embodiments, an anti-[protein x] (e.g., CD3) antibody binds to an epitope of [protein x] (e.g., CD3) that is conserved among [protein x] (e.g., CD3) from different species.

[0046] The term "Fc domain" or "Fc region" herein is used to define the C-terminal region of an immunoglobulin heavy chain containing at least a portion of the constant region. This term includes native-sequence Fc regions and variant Fc regions. In one embodiment, a human IgG heavy chain Fc region extends from Cys226 or from Pro230 to the carboxyl terminus of the heavy chain. However, antibodies produced by host cells may undergo post-translational truncation of one or more, particularly one or two, amino acids from the C-terminus of the heavy chain. Thus, antibodies produced by host cells by expression of a particular nucleic acid molecule encoding a full-length heavy chain may contain a full-length heavy chain or a truncated variant of the full-length heavy chain. This is the case when the last two C-terminal amino acids of the heavy chain are glycine (G446) and lysine (K447, according to the Kabat EU index). Thus, the C-terminal lysine (Lys447) or C-terminal glycine (Gly446) and lysine (Lys447) of the Fc region may or may not be present. The amino acid sequence of a heavy chain comprising an Fc region (or a subunit of an Fc domain as defined herein) is shown herein without the C-terminal glycine-lysine dipeptide, unless otherwise indicated. In one aspect, a heavy chain comprising an Fc region (subunit) as specified herein, contained in a binding molecule according to the invention, comprises an additional C-terminal glycine-lysine dipeptide (G446 and K447, numbering according to the Kabat EU index). In one aspect, a heavy chain comprising an Fc region (subunit) as specified herein, contained in a binding molecule according to the invention, comprises an additional C-terminal glycine residue (G446, numbering according to the Kabat EU index). Unless otherwise specified herein, the numbering of amino acid residues in the Fc region or constant region is according to the EU numbering system, also known as the EU index, as described in Kabat et al., Sequences of Proteins of Immunological Interest, 5th Edition, Public Health Service, National Institutes of Health, Bethesda, MD, 1991 (see also supra).As used herein, a "subunit" of an Fc domain refers to one of the two polypeptides that form a dimeric Fc domain, i.e., a polypeptide comprising the C-terminal constant region of an immunoglobulin heavy chain capable of stable self-association. For example, a subunit of an IgG Fc domain comprises the IgG CH2 and IgG CH3 constant domains.

[0047] A "modification that promotes the association of a first subunit and a second subunit of an Fc domain" refers to manipulation of the peptide backbone or post-translational modification of an Fc domain subunit that reduces or prevents the association of a polypeptide containing the Fc domain subunit with an identical polypeptide to form a homodimer. As used herein, a modification that promotes association preferably includes separate modifications made to each of the two Fc domain subunits (i.e., the first and second subunits of the Fc domain) that are desired to associate, where the modifications are complementary to each other to promote the association of the two Fc domain subunits. For example, a modification that promotes association may alter the structure or charge of one or both of the Fc domain subunits to sterically or electrostatically favor their association, respectively. Thus, (hetero)dimerization occurs between a polypeptide containing a first Fc domain subunit and a polypeptide containing a second Fc domain subunit, which may not be identical in the sense that the additional components (e.g., antigen-binding domains) fused to each subunit are not the same. In some embodiments, the modification that promotes binding of the first and second subunits of the Fc domain comprises an amino acid mutation, specifically an amino acid substitution, in the Fc domain. In certain embodiments, the modification that promotes binding of the first and second subunits of the Fc domain comprises a separate amino acid mutation, specifically an amino acid substitution, in each of the two subunits of the Fc domain.

[0048] The term "effector function" refers to the biological activity attributable to the Fc region of an antibody, which varies depending on the antibody isotype. Examples of antibody effector functions include C1q binding and complement-dependent cytotoxicity (CDC); Fc receptor binding; antibody-dependent cell-mediated cytotoxicity (ADCC); antibody-dependent cellular phagocytosis (ADCP); cytokine secretion; immune complex-mediated antigen uptake by antigen-presenting cells; downregulation of cell surface receptors (e.g., B cell receptors); and B cell activation.

[0049] An "activating Fc receptor" is an Fc receptor that, following binding of the Fc domain of an antibody, triggers signaling events that stimulate the receptor-bearing cell to carry out an effector function. Human activating Fc receptors include FcγRIIIa (CD16a), FcγRI (CD64), FcγRIIa (CD32), and FcαRI (CD89).

[0050] Antibody-dependent cellular cytotoxicity (ADCC) is an immune mechanism that causes immune effector cells to lyse antibody-coated target cells. Target cells are cells to which an antibody or its derivative, including an Fc region, specifically binds via a protein portion generally N-terminal to the Fc region. As used herein, the term "reduced ADCC" is defined as either a reduction in the number of target cells lysed in a given time period with a given concentration of antibody in the medium surrounding the target cells, via the ADCC mechanism defined above, and / or an increase in the concentration of antibody in the medium surrounding the target cells required to achieve lysis of a given number of target cells in a given time period via the ADCC mechanism. Reduced ADCC is compared to unengineered ADCC mediated by the same antibody produced by the same type of host cell using the same standard production, purification, formulation, and storage methods (known to those skilled in the art). For example, an amino acid substitution that reduces ADCC mediated by an antibody containing its Fc domain is relative to ADCC mediated by the same antibody without this amino acid substitution in the Fc domain. Suitable assays for measuring ADCC are well known in the art (see, for example, PCT Publication Nos. WO 2006 / 082515 or WO 2012 / 130831).

[0051] "Decreased binding," e.g., decreased binding to an Fc receptor, refers to a decrease in affinity for the respective interaction, as measured, for example, by SPR. For clarity, the term also includes a decrease in affinity to zero (or below the detection limit of the analytical method), i.e., a complete loss of the interaction. Conversely, "increased binding" refers to an increase in binding affinity for the respective interaction.

[0052] With respect to a VH and / or VL, "non-antigen binding" means that the VH and VL, alone or in combination, are incapable of specific binding to an antigen, and in particular are incapable of specific binding to a human antigen. The absence of specific binding of such a VH and / or VL to an antigen (i.e., the absence of binding that can be distinguished from non-specific interactions) can be determined, for example, by ELISA or surface plasmon resonance.

[0053] "Affinity" refers to the strength of the sum total of non-covalent interactions between a single binding site of a molecule (e.g., an antibody) and its binding partner (e.g., an antigen). Unless otherwise specified, as used herein, "binding affinity" refers to the intrinsic binding affinity that reflects a 1:1 interaction between members of a binding pair (e.g., an antibody and an antigen). The affinity of a molecule X for its partner Y is generally determined by the dissociation constant (K D ) Affinity can be measured by well-established methods known in the art, including those described herein. A preferred method for measuring affinity is surface plasmon resonance (SPR).

[0054] As used herein, the terms "engineer, engineered, engineering" are intended to include any manipulation of the peptide backbone or post-translational modification of a naturally occurring or recombinant polypeptide or fragment thereof. Engineering includes modification of the amino acid sequence, modification of the glycosylation pattern or modification of the side groups of individual amino acids, as well as combinations of these techniques.

[0055] As used herein, the term "amino acid mutation" is intended to encompass amino acid substitution, deletion, insertion, and modification. Any combination of substitution, deletion, insertion, and modification can be performed to arrive at the final construct, provided that the final construct possesses the desired characteristics (e.g., decreased binding to Fc receptors or increased association with another peptide). Deletions and insertions in the amino acid sequence include deletions and insertions of amino and / or carboxy terminal amino acids. Preferred amino acid mutations are amino acid substitutions. For example, to alter the binding characteristics of the Fc region, non-conservative amino acid substitutions, i.e., replacing one amino acid with another amino acid having different structural and / or chemical properties, are particularly preferred. Amino acid substitutions include substitutions with unnatural amino acids or substitutions with natural amino acid derivatives of the 20 standard amino acids (e.g., 4-hydroxyproline, 3-methylhistidine, ornithine, homoserine, 5-hydroxylysine). Amino acid mutations can be generated using genetic or chemical methods well known in the art. Genetic methods can include site-directed mutagenesis, PCR, gene synthesis, etc. It is contemplated that methods other than genetic engineering, such as chemical modification, for modifying the side chain group of an amino acid may also be useful. Various names may be used herein to refer to the same amino acid mutation. For example, a proline to glycine substitution at position 329 of the Fc domain is referred to as 329G, G329, G 329 , P329G or Pro329Gly.

[0056] "Percent (%) amino acid sequence identity" with respect to a reference polypeptide sequence is defined as the percentage of amino acid residues in a candidate sequence that are identical to the amino acid residues in the reference polypeptide, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, without considering any conservative substitutions as part of the sequence identity. Alignment for determining percent amino acid sequence identity can be achieved in a variety of ways within the skill of the art, for example, using publicly available computer software such as BLAST, BLAST-2, Clustal W, Megalign (DNASTAR) software, or the FASTA program package. Those skilled in the art can determine appropriate parameters for aligning sequences, including any algorithms required to achieve maximum alignment over the full length of the sequences being compared. Alternatively, percent identity values ​​can be generated using the sequence comparison computer program ALIGN-2. The ALIGN-2 sequence comparison computer program was written by Genentech, Inc. and the source code is registered along with user documentation with the U.S. Copyright Office, Washington, DC 20559, U.S. Copyright Registration No. TXU510087, and is described in WO 2001 / 007611.

[0057] Unless otherwise specified, for purposes of this specification, percent amino acid sequence identity values ​​are generated using the ggsearch program in the FASTA package version 36.3.8c or later with the BLOSUM50 comparison matrix. The FASTA program package was created by W.R. Pearson and D.J. Lipman ("Improved Tools for Biological Sequence Analysis," PNAS 85 (1988) 2444-2448), W.R. Pearson ("Effective protein sequence comparison," Meth. Enzymol. 266 (1996) 227-258), and Pearson et al. (Genomics 46 (1997) 24-36), and is publicly available at www.fasta.bioch.virginia.edu / fasta_www2 / fasta_down.shtml or www.ebi.ac.uk / Tools / sss / fasta. Alternatively, sequences can be compared using the public server accessible at fasta.bioch.virginia.edu / fasta_www2 / index.cgi using the ggsearch(globalprotein:protein) program and default options (BLOSUM50; open:-10; ext:-2; Ktup=2), ensuring a global rather than local alignment. The percent amino acid identity is given in the output alignment header.

[0058] By "fused" is meant that the components (eg, a Fab molecule and an Fc domain subunit) are linked by a peptide bond, either directly or via one or more peptide linkers.

[0059] The terms "polynucleotide" or "nucleic acid molecule" include any compound and / or substance comprising a polymer of nucleotides. Each nucleotide is composed of a base, specifically a purine or pyrimidine base (i.e., cytosine (C), guanine (G), adenine (A), thymine (T), or uracil (U)), a sugar (i.e., deoxyribose or ribose), and a phosphate group. Nucleic acid molecules are often described by their base sequence, whereby the bases represent the primary (linear) structure of the nucleic acid molecule. The sequence of bases is typically represented 5' to 3'. As used herein, the term nucleic acid molecule encompasses deoxyribonucleic acid (DNA), e.g., complementary DNA (cDNA) and genomic DNA, ribonucleic acid (RNA), particularly messenger RNA (mRNA), synthetic forms of DNA or RNA, and mixed polymers containing two or more of these molecules. Nucleic acid molecules may be linear or circular. In addition, the term nucleic acid molecule includes both sense and antisense strands, and both single-stranded and double-stranded forms. Furthermore, the nucleic acid molecules described herein may contain naturally occurring or non-naturally occurring nucleotides. Examples of non-naturally occurring nucleotides include modified nucleotide bases with derivatized sugar or phosphate backbone linkages or chemically modified residues. Nucleic acid molecules also encompass DNA and RNA molecules suitable as vectors for directly expressing the binding molecule pairs or binding molecules of the present invention in vitro and / or in vivo, for example, in a host or patient. Such DNA (e.g., cDNA) or RNA (e.g., mRNA) vectors may be unmodified or modified. For example, mRNA may be chemically modified to improve the stability of the RNA vector and / or the expression of the encoded molecule, thereby enabling the mRNA to be injected into a subject to generate antibodies in vivo (see, e.g., Stadler et al. (2017) Nature Medicine 23:815-817, or EP 2101823).

[0060] An "isolated" nucleic acid molecule refers to a nucleic acid molecule that has been separated from a component of its natural environment. Isolated nucleic acid molecules include nucleic acid molecules contained in cells that ordinarily contain the nucleic acid molecule, but where the nucleic acid molecule is present extrachromosomally or at a chromosomal location that is different from its natural chromosomal location.

[0061] An "isolated polynucleotide (or nucleic acid) encoding a [binding molecule / binding molecule pair]" refers to one or more polynucleotide molecules encoding the polypeptide chains of a binding molecule, e.g., an antibody heavy and light chain (or fragments thereof), including such polynucleotide molecules in a single vector or in separate vectors, and including such polynucleotide molecules present in one or more locations in a host cell.

[0062] As used herein, the term "vector" refers to a nucleic acid molecule capable of propagating another nucleic acid to which it is linked. The term includes vectors that integrate into the genome of a host cell into which they are introduced, as well as vectors that act as self-replicating nucleic acid structures. Certain vectors are capable of directing the expression of nucleic acids to which they are operatively linked. Such vectors are referred to herein as "expression vectors."

[0063] The terms "host cell," "host cell line," and "host cell culture" are used interchangeably and refer to cells into which exogenous nucleic acid has been introduced, including the progeny of such cells. Host cells include "transformants" and "transformed cells," and include the primary transformed cell and progeny derived from the host cell, regardless of the number of passages. The progeny may not be completely identical in nucleic acid content to the parent cell, but may contain mutations. Mutant progeny that have the same function or biological activity as screened or selected for in the originally transformed cell are included herein. Host cells are any type of cell line that can be used to produce the binding molecules of the invention. Host cells include cultured cells, e.g., cultured mammalian cells, such as HEK cells, CHO cells, BHK cells, NS0 cells, SP2 / 0 cells, YO myeloma cells, P3X63 mouse myeloma cells, PER cells, PER.C6 cells, or hybridoma cells, to name just a few, yeast cells, insect cells, and plant cells, but also include cells contained in transgenic animals, transgenic plants, or cultured plants, or animal tissues. In one embodiment, the host cell of the invention is a eukaryotic cell, particularly a mammalian cell. In one embodiment, the host cell is not a cell within the human body.

[0064] The term "pharmaceutical composition" or "pharmaceutical formulation" refers to a preparation that is in a form that allows the biological activity of the active ingredients contained therein to be effective, and that does not contain additional ingredients that are unacceptably toxic to the subject to which the composition is administered.

[0065] A "pharmaceutically acceptable carrier" refers to an ingredient in a pharmaceutical composition or formulation, other than an active ingredient, that is non-toxic to a subject. Pharmaceutically acceptable carriers include, but are not limited to, buffers, excipients, stabilizers, or preservatives.

[0066] The term "cancer" refers to a physiological condition in mammals that is typically characterized by uncontrolled cell proliferation. Examples of cancer include, but are not limited to, carcinoma, lymphoma, blastoma, sarcoma, and leukemia. Non-limiting examples of cancer include blood cancers such as leukemia, bladder cancer, brain cancer, head and neck cancer, pancreatic cancer, bile duct cancer, thyroid cancer, lung cancer, breast cancer, ovarian cancer, uterine cancer, cervical cancer, endometrial cancer, esophageal cancer, colon cancer, colorectal cancer, rectal cancer, stomach cancer, prostate cancer, skin cancer, squamous cell carcinoma, sarcoma, bone cancer, and kidney cancer. Other cell proliferative disorders include, but are not limited to, tumors located in the abdomen, bone, breast, digestive system, liver, pancreas, peritoneum, endocrine glands (adrenal glands, parathyroid glands, pituitary gland, testes, ovaries, thymus, thyroid), eye, head and neck, nervous system (central and peripheral), lymphatic system, pelvis, skin, soft tissue, spleen, chest, and genitourinary system. Precancerous conditions or lesions and cancer metastases are also included.

[0067] "Solid tumor cancer" refers to a malignant tumor that forms a discrete tumor mass (including tumor metastases) located at a specific site within a patient's body, such as a sarcoma or carcinoma (as opposed to, for example, blood cancers such as leukemia, which do not generally form solid tumors). Non-limiting examples of solid tumor cancers include bladder cancer, brain cancer, head and neck cancer, pancreatic cancer, lung cancer, breast cancer, ovarian cancer, uterine cancer, cervical cancer, endometrial cancer, esophageal cancer, colon cancer, colorectal cancer, rectal cancer, stomach cancer, prostate cancer, skin cancer, squamous cell carcinoma, bone cancer, liver cancer, and kidney cancer. Other solid tumor cancers contemplated in the context of the present invention include, but are not limited to, neoplasms located in the abdomen, bone, breast, digestive system, liver, pancreas, peritoneum, endocrine glands (adrenal glands, parathyroid glands, pituitary gland, testes, ovaries, thymus, thyroid), eye, head and neck, nervous system (central and peripheral), lymphatic system, pelvis, skin, soft tissue, muscle, spleen, chest, and genitourinary system. Precancerous conditions or lesions and cancer metastases are also included.

[0068] [Protein x] (e.g., HER2)-positive cancer" or "cancer expressing [protein x] (e.g., HER2)" refers to a cancer characterized by expression or overexpression of [protein x] (e.g., HER2) in cancer cells. Expression of [protein x] (e.g., HER2) can be determined, for example, by quantitative real-time PCR (measuring [protein x] (e.g., HER2) mRNA levels), immunohistochemistry (IHC), or Western blot assay. In one embodiment, the cancer expresses [protein x] (e.g., HER2). In one embodiment, the cancer expresses [protein x] (e.g., HER2) in at least 20%, preferably at least 50% or at least 80% of tumor cells, as determined by immunohistochemistry (IHC) using an antibody specific for [protein x] (e.g., HER2).

[0069] As used herein, "treatment" (and grammatical variants thereof, e.g., "treat" or "treating") refers to clinical intervention in an attempt to alter the natural course of disease in the individual being treated, and may be performed prophylactically or during the course of clinical pathology. Desired effects of treatment include preventing the onset or recurrence of disease, alleviating symptoms, attenuating any direct or indirect pathological consequences of the disease, preventing metastasis, reducing the rate of disease progression, remission or palliation of the condition, and improving or improving the prognosis. In some embodiments, the binding molecule pairs of the invention are used to delay the onset of disease or to slow the progression of disease.

[0070] An "individual" or "subject" is a mammal. Mammals include, but are not limited to, domestic animals (e.g., cows, sheep, cats, dogs, and horses), primates (e.g., humans and non-human primates such as monkeys), rabbits, and rodents (e.g., mice and rats). In certain embodiments, the individual or subject is human.

[0071] An "effective amount" of an agent, eg, a pharmaceutical composition, refers to an amount effective, at dosages and for periods of time necessary, to achieve a desired therapeutic or prophylactic result.

[0072] The term "package insert" is used to refer to the instructions customarily included in commercial packaging of therapeutic products, which contain information about the indications, usage, dosage, administration, concomitant therapy, contraindications and / or warnings for the use of such therapeutic product.

[0073] binding molecule pair In a first aspect, the present invention provides a method for producing a medicament for the treatment of a pulmonary arthritis, comprising: (a) a first binding molecule comprising (i) a first antigen-binding domain capable of binding to a target antigen, (ii) a first portion of an effector domain, and (iii) a first complementarity domain capable of binding to the first portion of the effector domain; and (b) a binding molecule pair comprising (i) a second antigen-binding domain capable of binding to a target antigen, (ii) a second portion of the effector domain, and (iii) a second binding molecule comprising a second complementarity domain capable of binding to the second portion of the effector domain; the first and second portions of the effector domain can bind to each other to form a functional effector domain when the first antigen-binding domain and the second antigen-binding domain bind to a target antigen on a cell surface; The first complementarity domain and the second complementarity domain are bound to the first and second portions of the effector domain, respectively, and the first and second portions of the effector domain are not bound to each other, providing a binding molecule pair.

[0074] The binding molecule pairs described above and herein may (unless the context dictates otherwise) incorporate any of the features described below, either alone or in combination.

[0075] Effector domain According to the present invention, each binding molecule of a binding molecule pair comprises a portion of an effector domain that can form a functional effector domain when the antigen-binding domains of the binding molecules bind to their target antigen on the surface of a cell, and the individual portions of the effector domain are not functional effector domains (i.e., the individual portions of the effector domain do not have the function of a complete effector domain).

[0076] In some embodiments, the effector domain is a dimer.

[0077] A functional effector domain may exert a biological function such as binding to an antigen, activating a cell signaling pathway, or blocking a receptor.

[0078] In some embodiments, the effector domain is an antigen-binding domain. In particular embodiments, the effector domain is an anti-CD3 antigen-binding domain (i.e., an antigen-binding domain capable of binding to CD3).

[0079] In some embodiments, the functional effector domain can bind to an antigen. In some embodiments, individual portions of the effector domain cannot bind to an antigen. In particular embodiments, the antigen is a T cell antigen, particularly an activated T cell antigen. In even more particular embodiments, the antigen is CD3, particularly CD3ε. In some embodiments, the antigen is human CD3.

[0080] In some embodiments, the first portion of the effector domain comprises a heavy chain variable region (VH) and the second portion of the effector domain comprises a light chain variable region (VL). In some embodiments, the first portion of the effector domain is a heavy chain variable region (VH) and the second portion of the effector domain is a light chain variable region (VL). In some embodiments, the first portion of the effector domain consists of a heavy chain variable region (VH) and the second portion of the effector domain consists of a light chain variable region (VL). In some embodiments, the effector domain is an Fv molecule.

[0081] In some embodiments, the effector domain is a humanized antigen-binding domain (i.e., the antigen-binding domain of a humanized antibody). In some embodiments, the VH and / or VL of the effector domain are humanized variable regions. In some embodiments, the VH and / or VL of the effector domain comprise an acceptor human framework, such as a human immunoglobulin framework or a human consensus framework.

[0082] In certain embodiments, the VH of the effector domain comprises a heavy chain complementarity determining region (HCDR)1 of SEQ ID NO: 15, an HCDR2 of SEQ ID NO: 16, and an HCDR3 of SEQ ID NO: 17, and the VL of the effector domain comprises a light chain complementarity determining region (LCDR)1 of SEQ ID NO: 19, an LCDR2 of SEQ ID NO: 20, and an LCDR3 of SEQ ID NO: 21. In further embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 18, and / or the VL of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 22.

[0083] In some embodiments, the VH of the effector domain comprises one or more heavy chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the heavy chain variable region sequence of SEQ ID NO: 18. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 18. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 18. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 18. In particular embodiments, a VH sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions compared to the reference sequence, yet an antigen-binding domain comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 18. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 18. In some cases, the VH of the effector domain may comprise the amino acid sequence of SEQ ID NO: 18, including post-translational modifications of the sequence.

[0084] In some embodiments, the VL of the effector domain comprises one or more light chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the light chain variable region sequence of SEQ ID NO: 22. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 22. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95% identical to the amino acid sequence of SEQ ID NO: 22. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 98% identical to the amino acid sequence of SEQ ID NO: 22. In particular embodiments, a VL sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions compared to the reference sequence, yet an antigen-binding domain comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 22. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 22. Optionally, the VL of the effector domain may comprise the amino acid sequence of SEQ ID NO: 22, including post-translational modifications of the sequence.

[0085] In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 18, and the VL of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 22. In some embodiments, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 18, and the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 22.

[0086] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising a VH comprising the amino acid sequence of SEQ ID NO: 18 and a VL comprising the amino acid sequence of SEQ ID NO: 22. In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising the VH sequence of SEQ ID NO: 18 and the VL sequence of SEQ ID NO: 22.

[0087] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising a VH comprising the heavy chain CDR sequence of the VH of SEQ ID NO: 18 and a VL comprising the light chain CDR sequence of the VL of SEQ ID NO: 22. In some embodiments, the antigen-binding domain comprises the HCDR1, HCDR2, and HCDR3 amino acid sequences of the VH of SEQ ID NO: 18 and the LCDR1, LCDR2, and LCDR3 amino acid sequences of the VL of SEQ ID NO: 22.

[0088] In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 18 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VH of SEQ ID NO: 18. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 18 and a framework with at least 95% sequence identity to the framework sequence of the VH of SEQ ID NO: 18. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 18 and a framework with at least 98% sequence identity to the framework sequence of the VH of SEQ ID NO: 18.

[0089] In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 22 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VL of SEQ ID NO: 22. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 22 and a framework with at least 95% sequence identity to the framework sequence of the VL of SEQ ID NO: 22. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 22 and a framework with at least 98% sequence identity to the framework sequence of the VL of SEQ ID NO: 22.

[0090] In some embodiments, the effector domain is an antigen-binding domain that binds CD3 comprising a VH sequence as in any of the embodiments provided above and a VL sequence as in any of the embodiments provided above.

[0091] In further specific embodiments, the VH of the effector domain comprises a heavy chain complementarity determining region (HCDR)1 of SEQ ID NO: 23, an HCDR2 of SEQ ID NO: 24, and an HCDR3 of SEQ ID NO: 25, and the VL of the effector domain comprises a light chain complementarity determining region (LCDR)1 of SEQ ID NO: 27, an LCDR2 of SEQ ID NO: 28, and an LCDR3 of SEQ ID NO: 29. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 26, and / or the VL of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 30.

[0092] In some embodiments, the VH of the effector domain comprises one or more heavy chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the heavy chain variable region sequence of SEQ ID NO: 26. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 26. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 26. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 26. In particular embodiments, a VH sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions compared to the reference sequence, yet an antigen-binding domain comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 26. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 26. In some cases, the VH of the effector domain may comprise the amino acid sequence of SEQ ID NO: 26, including post-translational modifications of the sequence.

[0093] In some embodiments, the VL of the effector domain comprises one or more light chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the light chain variable region sequence of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95% identical to the amino acid sequence of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 98% identical to the amino acid sequence of SEQ ID NO: 30. In particular embodiments, a VL sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions compared to the reference sequence, yet an antigen-binding domain comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 30. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 30. Optionally, the VL of the effector domain may comprise the amino acid sequence of SEQ ID NO: 30, including post-translational modifications of the sequence.

[0094] In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 26, and the VL of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 30. In some embodiments, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 26, and the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 30.

[0095] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising a VH comprising the amino acid sequence of SEQ ID NO: 26 and a VL comprising the amino acid sequence of SEQ ID NO: 30. In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising the VH sequence of SEQ ID NO: 26 and the VL sequence of SEQ ID NO: 30.

[0096] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising a VH comprising the heavy chain CDR sequence of the VH of SEQ ID NO: 26 and a VL comprising the light chain CDR sequence of the VL of SEQ ID NO: 30. In some embodiments, the antigen-binding domain comprises the HCDR1, HCDR2, and HCDR3 amino acid sequences of the VH of SEQ ID NO: 26 and the LCDR1, LCDR2, and LCDR3 amino acid sequences of the VL of SEQ ID NO: 30.

[0097] In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 26 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VH of SEQ ID NO: 26. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 26 and a framework with at least 95% sequence identity to the framework sequence of the VH of SEQ ID NO: 26. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 26 and a framework with at least 98% sequence identity to the framework sequence of the VH of SEQ ID NO: 26.

[0098] In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 30 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VL of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 30 and a framework with at least 95% sequence identity to the framework sequence of the VL of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 30 and a framework with at least 98% sequence identity to the framework sequence of the VL of SEQ ID NO: 30.

[0099] In some embodiments, the effector domain is an antigen-binding domain that binds CD3 comprising a VH sequence as in any of the embodiments provided above and a VL sequence as in any of the embodiments provided above.

[0100] In still other embodiments, the VH of the effector domain comprises a heavy chain complementarity determining region (HCDR)1 of SEQ ID NO: 31, an HCDR2 of SEQ ID NO: 32, and an HCDR3 of SEQ ID NO: 33, and the VL of the effector domain comprises a light chain complementarity determining region (LCDR)1 of SEQ ID NO: 35, an LCDR2 of SEQ ID NO: 36, and an LCDR3 of SEQ ID NO: 37. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 34, and / or the VL of the effector comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 38.

[0101] In some aspects, the VH of the effector domain comprises one or more heavy chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the heavy chain variable region sequence of SEQ ID NO: 34. In some aspects, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 34. In some aspects, the VH of the effector domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 34. In some aspects, the VH of the effector domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 34. In certain embodiments, a VH sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions relative to the reference sequence, yet the binding site comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 34. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 34. Optionally, the VH of the effector domain may comprise the amino acid sequence of SEQ ID NO: 34, including post-translational modifications of the sequence.

[0102] In some embodiments, the VL of the effector domain comprises one or more light chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the light chain variable region sequence of SEQ ID NO: 38. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 38. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95% identical to the amino acid sequence of SEQ ID NO: 38. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 98% identical to the amino acid sequence of SEQ ID NO: 38. In particular embodiments, a VL sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions compared to the reference sequence, yet an antigen-binding domain comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 38. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 38. Optionally, the VL of the effector domain may comprise the amino acid sequence of SEQ ID NO: 38, including post-translational modifications of the sequence.

[0103] In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 34, and the VL of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 38. In some embodiments, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 34, and the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 38.

[0104] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising a VH comprising the amino acid sequence of SEQ ID NO: 34 and a VL comprising the amino acid sequence of SEQ ID NO: 38. In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising the VH sequence of SEQ ID NO: 34 and the VL sequence of SEQ ID NO: 38.

[0105] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising a VH comprising the heavy chain CDR sequence of the VH of SEQ ID NO: 34 and a VL comprising the light chain CDR sequence of the VL of SEQ ID NO: 38. In some embodiments, the antigen-binding domain comprises the HCDR1, HCDR2, and HCDR3 amino acid sequences of the VH of SEQ ID NO: 34 and the LCDR1, LCDR2, and LCDR3 amino acid sequences of the VL of SEQ ID NO: 38.

[0106] In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 34 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VH of SEQ ID NO: 34. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 34 and a framework with at least 95% sequence identity to the framework sequence of the VH of SEQ ID NO: 34. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 34 and a framework with at least 98% sequence identity to the framework sequence of the VH of SEQ ID NO: 34.

[0107] In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 38 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VL of SEQ ID NO: 38. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 38 and a framework with at least 95% sequence identity to the framework sequence of the VL of SEQ ID NO: 38. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 38 and a framework with at least 98% sequence identity to the framework sequence of the VL of SEQ ID NO: 38.

[0108] In some embodiments, the effector domain is an antigen-binding domain that binds CD3, particularly an Fv molecule, comprising a VH sequence as in any of the embodiments provided above and a VL sequence as in any of the embodiments provided above.

[0109] In other embodiments, the VH of the effector domain comprises a heavy chain complementarity determining region (HCDR)1 of SEQ ID NO: 23, an HCDR2 of SEQ ID NO: 24, and an HCDR3 of SEQ ID NO: 60, and the VL of the effector domain comprises a light chain complementarity determining region (LCDR)1 of SEQ ID NO: 27, an LCDR2 of SEQ ID NO: 28, and an LCDR3 of SEQ ID NO: 29. In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 61, and / or the VL of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 30.

[0110] In some aspects, the VH of the effector domain comprises one or more heavy chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the heavy chain variable region sequence of SEQ ID NO: 61. In some aspects, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 61. In some aspects, the VH of the effector domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 61. In some aspects, the VH of the effector domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 61. In certain embodiments, a VH sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions relative to the reference sequence, but the binding site comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 61. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 61. In some cases, the VH of the effector domain may comprise the amino acid sequence of SEQ ID NO: 61, including post-translational modifications of the sequence.

[0111] In some embodiments, the VL of the effector domain comprises one or more light chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the light chain variable region sequence of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 95% identical to the amino acid sequence of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises an amino acid sequence at least about 98% identical to the amino acid sequence of SEQ ID NO: 30. In particular embodiments, a VL sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions compared to the reference sequence, yet an antigen-binding domain comprising that sequence retains the ability to bind to CD3. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 30. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 30. Optionally, the VL of the effector domain may comprise the amino acid sequence of SEQ ID NO: 30, including post-translational modifications of the sequence.

[0112] In some embodiments, the VH of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 61, and the VL of the effector domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 30. In some embodiments, the VH of the effector domain comprises the amino acid sequence of SEQ ID NO: 61, and the VL of the effector domain comprises the amino acid sequence of SEQ ID NO: 30.

[0113] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising a VH comprising the amino acid sequence of SEQ ID NO: 61 and a VL comprising the amino acid sequence of SEQ ID NO: 30. In some embodiments, the effector domain is an antigen-binding domain that binds to CD3 comprising the VH sequence of SEQ ID NO: 61 and the VL sequence of SEQ ID NO: 30.

[0114] In some embodiments, the effector domain is an antigen-binding domain that binds to CD3, comprising a VH comprising the heavy chain CDR sequence of the VH of SEQ ID NO: 61 and a VL comprising the light chain CDR sequence of the VL of SEQ ID NO: 30. In some embodiments, the antigen-binding domain comprises the HCDR1, HCDR2, and HCDR3 amino acid sequences of the VH of SEQ ID NO: 61 and the LCDR1, LCDR2, and LCDR3 amino acid sequences of the VL of SEQ ID NO: 30.

[0115] In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 61 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VH of SEQ ID NO: 61. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 61 and a framework with at least 95% sequence identity to the framework sequence of the VH of SEQ ID NO: 61. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 61 and a framework with at least 98% sequence identity to the framework sequence of the VH of SEQ ID NO: 61.

[0116] In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 30 and a framework with at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VL of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 30 and a framework with at least 95% sequence identity to the framework sequence of the VL of SEQ ID NO: 30. In some embodiments, the VL of the effector domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 30 and a framework with at least 98% sequence identity to the framework sequence of the VL of SEQ ID NO: 30.

[0117] In some embodiments, the effector domain is an antigen-binding domain that binds CD3 comprising a VH sequence as in any of the embodiments provided above and a VL sequence as in any of the embodiments provided above.

[0118] Complementarity domain According to the present invention, each binding molecule of a binding molecule pair comprises a complementary domain that associates with portions of the effector domains in such binding molecules, but the effector domain portions do not associate with each other.

[0119] The complementary domain is complementary to a respective portion of the effector domain, but does not form a functional effector domain with the respective portion of the effector domain.

[0120] In some embodiments, the first and second complementary domains cannot form a functional effector domain with a portion of the effector domain. In some embodiments, the first and second complementary domains do not form a functional effector domain when associated with a portion of the effector domain. In some embodiments, the first portion of the effector domain and the first complementary domain and / or the second portion of the effector domain and the second complementary domain do not form a functional effector domain when bound to each other.

[0121] The complementary domains may also be complementary to each other.

[0122] In some embodiments, the first and second complementary domains can bind to one another, hi some embodiments, the first complementary domain and the second complementary domain bind to one another when the first and second portions of the effector domain are associated with one another.

[0123] In some embodiments, the first complementary domain comprises a VL and the second complementary domain comprises a VH. In some embodiments, the first complementary domain is a VL and the second complementary domain is a VH. In some embodiments, the first complementary domain consists of a VL and the second complementary domain consists of a VH.

[0124] In some embodiments, the VH and VL complementary domains are non-antigen binding (either alone (i.e., not bound to each other) or in combination (i.e., bound to each other, as in antigen-binding domains)).

[0125] In some embodiments, the VH of the second complementarity domain comprises a heavy chain complementarity determining region (HCDR)1 of SEQ ID NO: 47, an HCDR2 of SEQ ID NO: 48, and an HCDR3 of SEQ ID NO: 49, and the VL of the first complementarity domain comprises a light chain complementarity determining region (LCDR)1 of SEQ ID NO: 51, an LCDR2 of SEQ ID NO: 52, and an LCDR3 of SEQ ID NO: 53. In some embodiments, the VH of the second complementarity domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 50, and / or the VL of the first complementarity domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 54.

[0126] In some embodiments, the VH of the second complementarity domain comprises one or more heavy chain framework sequences (i.e., FR1, FR2, FR3 and / or FR4 sequences) of the heavy chain variable region sequence of SEQ ID NO: 50. In some embodiments, the VH of the second complementarity domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 50. In some embodiments, the VH of the second complementarity domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 50. In some embodiments, the VH of the second complementarity domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 50. In some embodiments, the VH of the second complementarity domain comprises the amino acid sequence of SEQ ID NO: 50. Optionally, the VH of the second complementarity domain comprises the amino acid sequence of SEQ ID NO: 50, including post-translational modifications of the sequence.

[0127] In some embodiments, the VL of the first complementarity domain comprises one or more light chain framework sequences (i.e., the FR1, FR2, FR3 and / or FR4 sequences) of the light chain variable region sequence of SEQ ID NO: 54. In some embodiments, the VL of the first complementarity domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 54. In some embodiments, the VL of the first complementarity domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 54. In some embodiments, the VL of the first complementarity domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 54. In some embodiments, the VL of the first complementarity domain comprises the amino acid sequence of SEQ ID NO: 54. Optionally, the VL of the first complementarity domain comprises the amino acid sequence of SEQ ID NO: 54, including post-translational modifications of the sequence.

[0128] In some embodiments, the VH of the second complementarity domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 50, and the VL of the first complementarity domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 54. In some embodiments, the VH of the second complementarity domain comprises the amino acid sequence of SEQ ID NO: 50, and the VL of the first complementarity domain comprises the amino acid sequence of SEQ ID NO: 54.

[0129] In some embodiments, the first and second complementary domains are part of a non-antigen binding domain comprising a VH comprising the amino acid sequence of SEQ ID NO: 50, and a VL comprising the amino acid sequence of SEQ ID NO: 54. In some embodiments, the first and second complementary domains are part of a non-antigen binding domain comprising the VH sequence of SEQ ID NO: 50 and the VL sequence of SEQ ID NO: 54.

[0130] In some embodiments, the first and second complementarity domains are part of a non-antigen binding domain comprising a VH comprising the heavy chain CDR sequence of the VH of SEQ ID NO: 50, and a VL comprising the light chain CDR sequence of the VL of SEQ ID NO: 54. In some embodiments, the non-antigen binding domain comprises the HCDR1, HCDR2, and HCDR3 amino acid sequences of the VH of SEQ ID NO: 50, and the LCDR1, LCDR2, and LCDR3 amino acid sequences of the VL of SEQ ID NO: 54.

[0131] In some embodiments, the VH of the second complementarity domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 50 and a framework of at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VH of SEQ ID NO: 50. In some embodiments, the VH of the second complementarity domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 50 and a framework of at least 95% sequence identity to the framework sequence of the VH of SEQ ID NO: 50. In some embodiments, the VH of the second complementarity domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 50 and a framework of at least 98% sequence identity to the framework sequence of the VH of SEQ ID NO: 50.

[0132] In some embodiments, the VL of the first complementarity domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 54 and a framework of at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VL of SEQ ID NO: 54. In some embodiments, the VL of the first complementarity domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 54 and a framework of at least 95% sequence identity to the framework sequence of the VL of SEQ ID NO: 54. In some embodiments, the VL of the first complementarity domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 54 and a framework of at least 98% sequence identity to the framework sequence of the VL of SEQ ID NO: 54.

[0133] In some embodiments, the first and second complementarity domains are part of a non-antigen binding domain comprising a VH sequence as in any of the embodiments provided above, and a VL sequence as in any of the embodiments provided above.

[0134] In some embodiments, the first portion of the effector domain comprises a first VH, the first complementary domain comprises a first VL, the second portion of the effector domain comprises a second VL, and the second complementary domain comprises a second VH. In some embodiments, the first portion of the effector domain is a first VH, the first complementary domain is a first VL, the second portion of the effector domain is a second VL, and the second complementary domain is a second VH. In some embodiments, the first portion of the effector domain consists of a first VH, the first complementary domain consists of a first VL, the second portion of the effector domain consists of a second VL, and the second complementary domain consists of a second VH.

[0135] In some embodiments, the first portion of the effector domain and the first complementary domain, and / or the second portion of the effector domain and the second complementary domain are fused to each other, ie, the first portion of the effector domain is fused at its C-terminus to the N-terminus of the first complementary domain, and / or the second portion of the effector domain is fused at its C-terminus to the N-terminus of the second complementary domain.

[0136] Charged residue The complementary domain and / or the effector domain portion may contain amino acid substitutions, particularly substitutions with charged amino acid residues, to adjust the affinity between the complementary domain and / or the effector domain portion. For example, introducing amino acid residues of opposite charge into the two complementary domains will improve the affinity of the two complementary domains to each other (thus increasing the strength and tendency of the two complementary domains to associate with each other). Conversely, introducing amino acid residues of the same charge into the two complementary domains will reduce the affinity of the two complementary domains to each other (thus reducing the strength and tendency of the two complementary domains to associate with each other). The same can be applied to the two portions of the effector domain.

[0137] In some embodiments, each of the second VH and first VL and / or each of the first VH and second VL according to the above embodiments, particularly each of the second VH and first VL, comprises an amino acid substitution in which an amino acid residue is replaced with a charged replacement amino acid residue, and (i) the substituted amino acid residue in the VH and VL has an opposite charge, or (ii) the substituted amino acid residue in the VH and VL has the same charge.

[0138] In another embodiment, each of the first VH and first VL and / or each of the second VH and second VL comprises an amino acid substitution in which an amino acid residue is replaced with a charged replacement amino acid residue, and (i) the substituted amino acid residue in the VH and VL has an opposite charge, or (ii) the substituted amino acid residue in the VH and VL has the same charge.

[0139] In some embodiments, (i) the substituted amino acid residue in VH is a positively charged amino acid residue and the substituted amino acid residue in VL is a negatively charged amino acid residue, or the substituted amino acid residue in VH is a negatively charged amino acid residue and the substituted amino acid residue in VL is a positively charged amino acid residue, or (ii) the substituted amino acid residues in VH and VL are each positively charged amino acid residues, or the substituted amino acid residues in VH and VL are each negatively charged amino acid residues. In some embodiments, the positively charged amino acid residue is lysine (K), arginine (R), or histidine (H), specifically lysine (K) or arginine (R), and most specifically lysine (K). In some embodiments, the negatively charged amino acid residue is glutamic acid (E) or aspartic acid (D), specifically glutamic acid (E).

[0140] In some embodiments, the amino acid substitutions are in the framework regions of VH and VL.

[0141] In some embodiments, the amino acid substitutions are at the interface between the VH and VL (when bound to each other).

[0142] In some embodiments, the amino acid substitutions are at position 39 of the VH and position 38 of the VL (numbering according to the Kabat EU index).

[0143] In some embodiments, the amino acid substitution in VH is Q39K or Q39E and / or the amino acid substitution in VL is Q38K or Q38E (numbering according to the Kabat EU index).

[0144] In some aspects, the amino acid substitution in VH is Q39K and the amino acid substitution in VL is Q38E; the amino acid substitution in VH is Q39E and the amino acid substitution in VL is Q38K; the amino acid substitution in VH is Q39K and the amino acid substitution in VL is Q38K; or the amino acid substitution in VH is Q39E and the amino acid substitution in VL is Q38E.

[0145] Suitable amino acid substitutions are also described, for example, in Igawa et al. (Prot Eng Des Sel (2010) 23, 667-677) or European Patent Application No. 1870459(A1), which is incorporated herein by reference in its entirety.

[0146] antigen-binding domain According to the present invention, each binding molecule of a binding molecule pair comprises an antigen-binding domain capable of binding to one or more target antigens. Binding of the binding molecules to their target antigens on the surface of a cell via their antigen-binding domains allows the two portions of the effector domain to associate with each other to form a functional effector domain.

[0147] Without wishing to be bound by theory, when the two portions of the effector domain are brought into sufficient proximity to each other (through binding of the binding molecules to their target antigens on the surface of a cell), they dissociate from their respective complementary domains and instead associate with each other to form a functional effector domain.

[0148] The binding of each binding molecule can be monovalent (i.e., a binding molecule that comprises only a single antigen-binding domain) or multivalent, e.g., bivalent (i.e., a binding molecule that comprises two or more, e.g., two, antigen-binding domains).

[0149] Each of the binding molecules may be monospecific (i.e., all binding domains of the binding molecule bind to the same target antigen) or multispecific, e.g., bispecific (i.e., at least one antigen-binding domain of the binding molecule binds to one target antigen and at least one antigen-binding domain of the binding molecule binds to a different target antigen).

[0150] Furthermore, the binding molecules included in a binding molecule pair according to the invention can have the same or different binding specificities (i.e., both binding molecules bind to the same target antigen, or the two binding molecules bind to different target antigens).

[0151] In some embodiments, the first binding molecule comprises a third antigen-binding domain capable of binding to the target antigen, and / or the second binding molecule comprises a fourth antigen-binding domain capable of binding to the target antigen.

[0152] In some embodiments, each binding molecule comprises a single antigen-binding domain capable of binding to the target antigen, hi other embodiments, each binding molecule comprises two antigen-binding domains capable of binding to the target antigen.

[0153] In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) is an antigen-binding domain selected from the group consisting of an Fv molecule, an scFv molecule, a Fab molecule, and a single domain antibody.

[0154] In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) are Fab molecules. In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) are each Fab molecules.

[0155] In some embodiments, each binding molecule comprises a single antigen-binding domain capable of binding to a target antigen, and the antigen-binding domain is a Fab molecule. In other embodiments, each binding molecule comprises two antigen-binding domains capable of binding to a target antigen, and the antigen-binding domains are Fab molecules.

[0156] In some embodiments, the first antigen-binding domain and the second antigen-binding domain bind to the same target antigen, hi some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) bind to the same target antigen.

[0157] In some embodiments, the first antigen-binding domain and the second antigen-binding domain bind to different target antigens, hi some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) bind to different target antigens.

[0158] In some embodiments, the first antigen-binding domain and the second antigen-binding domain bind to the same target antigen, the third antigen-binding domain (if present) and the fourth antigen-binding domain (if present) bind to the same target antigen, and the target antigen bound by the first antigen-binding domain and the second antigen-binding domain is different from the target antigen bound by the third antigen-binding domain (if present) and the fourth antigen-binding domain (if present).

[0159] In certain embodiments, the first and third antigen-binding domains (if present) bind to the same target antigen, the second and fourth antigen-binding domains (if present) bind to the same target antigen, and the target antigen bound by the first and third antigen-binding domains (if present) is different from the target antigen bound by the second and fourth antigen-binding domains (if present).

[0160] In some embodiments, the effector domain is an antigen-binding domain, and the target antigens of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) are different from the antigen bound by the effector domain (i.e., the antigen to which a functional effector domain can bind, e.g., CD3). In some embodiments, the effector domain is an antigen-binding domain, and none of the antigen-binding domains of the first binding molecule and the second binding molecule can bind to the antigen bound by the effector domain (i.e., the antigen to which a functional effector domain can bind, e.g., CD3).

[0161] In some embodiments, the target antigen of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) is not CD3, particularly human CD3. In some embodiments, none of the antigen-binding domains of the first and second binding molecules can bind to CD3, particularly human CD3.

[0162] In some embodiments, the target antigens of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) are expressed on the same cell, on adjacent cells, or on cells in the same tissue (i.e., cells that are near each other, even if they are not the same). In some embodiments, the target antigens of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) are expressed on the same cell.

[0163] In some embodiments, the cell is a tumor cell (e.g., a cancer cell or a tumor stromal cell, particularly a cancer cell). In some embodiments, the target antigen of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) is a tumor antigen.

[0164] An exemplary target antigen is HER2.

[0165] In some embodiments, the target antigen of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) is HER2. In some embodiments, the target antigen of the first antigen-binding domain and the second antigen-binding domain is HER2. In some embodiments, the target antigen of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) is HER2.

[0166] In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) comprise a heavy chain variable region (VH) and a light chain variable region (VL).

[0167] In some embodiments, the antigen-binding domain is a humanized antigen-binding domain (i.e., the antigen-binding domain of a humanized antibody). In some embodiments, the VH and / or VL of the antigen-binding domain are humanized variable regions. In some embodiments, the VH and / or VL of the antigen-binding domain comprise an acceptor human framework, e.g., a human immunoglobulin framework or a human consensus framework.

[0168] The following embodiments relate to the VH and VL of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present), wherein the antigen-binding domain is capable of binding to HER2 (i.e., the target antigen of the antigen-binding domain is HER2).

[0169] In some embodiments, the VH of the antigen-binding domain comprises a heavy chain complementarity determining region (HCDR)1 of SEQ ID NO: 39, an HCDR2 of SEQ ID NO: 40, and an HCDR3 of SEQ ID NO: 41, and the VL of the antigen-binding domain comprises a light chain complementarity determining region (LCDR)1 of SEQ ID NO: 43, an LCDR2 of SEQ ID NO: 44, and an LCDR3 of SEQ ID NO: 45. In further embodiments, the VH of the antigen-binding domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 42, and / or the VL of the antigen-binding domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 46.

[0170] In some aspects, the VH of the antigen-binding domain comprises one or more heavy chain framework sequences (i.e., FR1, FR2, FR3 and / or FR4 sequences) of the heavy chain variable region sequence of SEQ ID NO: 42. In some aspects, the VH of the antigen-binding domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 42. In some aspects, the VH of the antigen-binding domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 42. In some aspects, the VH of the antigen-binding domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 42. In certain embodiments, a VH sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions relative to the reference sequence, but the binding site comprising that sequence retains the ability to bind to HER2. In certain aspects, a total of 1 to 10 amino acids are substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 42. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VH of the antigen-binding domain comprises the amino acid sequence of SEQ ID NO: 42. Optionally, the VH of the antigen-binding domain comprises the amino acid sequence of SEQ ID NO: 42, including post-translational modifications of the sequence.

[0171] In some embodiments, the VL of the antigen-binding domain comprises one or more light chain framework sequences (i.e., FR1, FR2, FR3 and / or FR4 sequences) of the light chain variable region sequence of SEQ ID NO: 46. In some embodiments, the VL of the antigen-binding domain comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 46. In some embodiments, the VL of the antigen-binding domain comprises an amino acid sequence that is at least about 95% identical to the amino acid sequence of SEQ ID NO: 46. In some embodiments, the VL of the antigen-binding domain comprises an amino acid sequence that is at least about 98% identical to the amino acid sequence of SEQ ID NO: 46. In certain embodiments, a VL sequence with at least 95%, 96%, 97%, 98%, or 99% identity contains substitutions (e.g., conservative substitutions), insertions, or deletions compared to the reference sequence, but the antigen-binding domain comprising that sequence retains the ability to bind to HER2. In certain aspects, a total of 1 to 10 amino acids have been substituted, inserted, and / or deleted in the amino acid sequence of SEQ ID NO: 46. In certain embodiments, the substitutions, insertions, or deletions occur in regions outside the CDRs (i.e., in the FRs). In some aspects, the VL of the antigen-binding domain comprises the amino acid sequence of SEQ ID NO: 46. Optionally, the VL of the antigen-binding domain comprises the amino acid sequence of SEQ ID NO: 42, including post-translational modifications of the sequence.

[0172] In some embodiments, the VH of the antigen-binding domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 42, and / or the VL of the antigen-binding domain comprises an amino acid sequence at least about 95%, 96%, 97%, 98%, or 99% identical to the amino acid sequence of SEQ ID NO: 46. In some embodiments, the VH of the antigen-binding domain comprises the amino acid sequence of SEQ ID NO: 42, and the VL of the antigen-binding domain comprises the amino acid sequence of SEQ ID NO:46.

[0173] In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) is an antigen-binding domain that binds to HER2 comprising a VH comprising the amino acid sequence of SEQ ID NO: 42 and a VL comprising the amino acid sequence of SEQ ID NO: 46. In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) is an antigen-binding domain that binds HER2 comprising the VH sequence of SEQ ID NO: 42 and the VL sequence of SEQ ID NO: 46.

[0174] In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) is an antigen-binding domain that binds to HER2, comprising a VH comprising the heavy chain CDR sequence of the VH of SEQ ID NO: 42 and a VL comprising the light chain CDR sequence of the VL of SEQ ID NO: 46. In some embodiments, the antigen-binding domain comprises the HCDR1, HCDR2, and HCDR3 amino acid sequences of the VH of SEQ ID NO: 42 and the LCDR1, LCDR2, and LCDR3 amino acid sequences of the VL of SEQ ID NO: 46.

[0175] In some embodiments, the VH of the antigen binding domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 42 and a framework having at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VH of SEQ ID NO: 42. In some embodiments, the VH of the effector domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 42 and a framework having at least 95% sequence identity to the framework sequence of the VH of SEQ ID NO: 42. In some embodiments, the VH of the antigen binding domain comprises the heavy chain CDR sequence of the VH of SEQ ID NO: 42 and a framework having at least 98% sequence identity to the framework sequence of the VH of SEQ ID NO: 42.

[0176] In some embodiments, the VL of the antigen binding domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 46 and a framework having at least 95%, 96%, 97%, 98% or 99% sequence identity to the framework sequence of the VL of SEQ ID NO: 46. In some embodiments, the VL of the antigen binding domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 46 and a framework having at least 95% sequence identity to the framework sequence of the VL of SEQ ID NO: 46. In some embodiments, the VL of the antigen binding domain comprises the light chain CDR sequence of the VL of SEQ ID NO: 46 and a framework having at least 98% sequence identity to the framework sequence of the VL of SEQ ID NO: 46.

[0177] In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) is an antigen-binding domain that binds to HER2, particularly a Fab molecule, comprising a VH sequence as in any of the embodiments provided above and a VL sequence as in any of the embodiments provided above.

[0178] In some embodiments, the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) are each antigen-binding domains that bind to HER2, particularly Fab molecules, comprising a VH sequence as in any of the embodiments provided above and a VL sequence as in any of the embodiments provided above.

[0179] Fc domain According to the present invention, the first binding molecule and / or the second binding molecule may comprise an Fc domain.

[0180] The Fc domain of a binding molecule consists of a pair of polypeptide chains containing the heavy chain domains of an immunoglobulin molecule. For example, the Fc domain of an immunoglobulin G (IgG) molecule is a dimer, with each subunit containing the CH2 and CH3 IgG heavy chain constant domains. The two subunits of the Fc domain can form a stable association with each other.

[0181] In some embodiments, the first binding molecule comprises a first Fc domain comprised of a first subunit and a second subunit, and / or the second binding molecule comprises a second Fc domain comprised of a first subunit and a second subunit. In some embodiments, the first binding molecule comprises a first Fc domain comprised of a first subunit and a second subunit, and the second binding molecule comprises a second Fc domain comprised of a first subunit and a second subunit. In some embodiments, each of the binding molecules comprises no more than one Fc domain.

[0182] In some embodiments, the first Fc domain and / or the second Fc domain is an IgG Fc domain. In a particular embodiment, the Fc domain is an IgG1 Fc domain. In another embodiment, the Fc domain is an IgG4 Fc domain. In a more specific embodiment, the Fc domain is an IgG4 Fc domain comprising an amino acid substitution at position S228 (Kabat EU index numbering), in particular the amino acid substitution S228P. This amino acid substitution reduces Fab arm exchange of IgG4 antibodies in vivo (see Stubenrauch et al., Drug Metabolism and Disposition 38, 84-91 (2010)). In a further embodiment, the Fc domain is a human Fc domain. In a particular embodiment, the Fc domain is a human IgG1 Fc domain. An exemplary sequence of a human IgG1 Fc region is given in SEQ ID NO: 59.

[0183] In some embodiments, the Fc domain comprises a modification that promotes association of the first and second subunits of the Fc domain. Fc domain modifications that promote heterodimerization are further described below.

[0184] In some embodiments, the Fc domain comprises one or more amino acid substitutions that reduce Fc receptor binding and / or effector function. Fc domain modifications that reduce Fc receptor binding and / or effector function are further described herein below.

[0185] In some embodiments, the first and third antigen-binding domains (if present) are each fused to the first Fc domain subunit, and / or the second and fourth antigen-binding domains (if present) are each fused to the second Fc domain subunit. In some embodiments, the first and third antigen-binding domains (if present) are each fused at their C-terminus to the N-terminus of the first Fc domain subunit, and / or the second and fourth antigen-binding domains (if present) are each fused at their C-terminus to the N-terminus of the second Fc domain subunit.

[0186] a) Fc domain modifications that promote heterodimerization The binding molecule according to the present invention comprises a portion of the effector domain, a complementary domain, and one or more antigen-binding domains that can be fused to one or the other of the two subunits of the Fc domain, which are typically contained in two non-identical polypeptide chains. Recombinant coexpression of these polypeptides and subsequent dimerization results in several possible combinations of the two polypeptides. Therefore, to improve the yield and purity of the binding molecule in recombinant production, it would be advantageous to introduce modifications into the Fc domain of the binding molecule that promote binding of the desired polypeptide.

[0187] Thus, in certain embodiments, the Fc domain of a binding molecule according to the invention comprises a modification that promotes binding of the first and second subunits of the Fc domain. The longest site of protein-protein interaction between the two subunits of a human IgG Fc domain is within the CH3 domain of the Fc domain. Thus, in some embodiments, the modification is within the CH3 domain of the Fc domain.

[0188] Several approaches exist for modifications in the CH3 domain of the Fc domain to enhance heterodimerization, and are fully described, for example, in WO 96 / 27011, WO 98 / 050431, EP 1870459, WO 2007 / 110205, WO 2007 / 147901, WO 2009 / 089004, WO 2010 / 129304, WO 2011 / 90754, WO 2011 / 143545, WO 2012058768, WO 2013157954, WO 2013096291. Typically, in all such approaches, the CH3 domain of the first Fc domain subunit and the CH3 domain of the second Fc domain subunit are both engineered in a complementary manner such that each CH3 domain (or the heavy chain comprising it) is directed not to homodimerize with itself but to heterodimerize with another complementary engineered CH3 domain (such that the first CH3 domain and the second CH3 domain heterodimerize, and no homodimers are formed between the two first CH3 domains or the two second CH3 domains).

[0189] In certain embodiments, the modification that promotes binding of the first and second subunits of the Fc domain is a so-called "knob-into-hole" modification, which comprises a "knob" modification on one of the two subunits of the Fc domain and a "hole" modification on the other of the two subunits of the Fc domain.

[0190] Knob-into-hole technology is described, for example, in U.S. Patent No. 5,731,168, U.S. Patent No. 7,695,936, Ridgway et al., Prot Eng 9, 617-621 (1996), and Carter, J Immunol Meth 248, 7-15 (2001). Typically, this method involves promoting heterodimer formation and preventing homodimer formation by introducing a protuberance ("knob") at the interface of a first polypeptide and a corresponding cavity at the interface of a second polypeptide, so that the protuberance can be positioned within the corresponding cavity. The protuberance is constructed by replacing a small amino acid side chain from the interface of the first polypeptide with a larger one (e.g., tyrosine or tryptophan). A compensatory cavity of the same or similar size as the protuberance is created at the interface of the second polypeptide by replacing the large amino acid side chain with a small one (e.g., alanine or threonine).

[0191] Thus, in a preferred embodiment, in the CH3 domain of a first subunit of an Fc domain of a binding molecule, an amino acid residue is replaced with an amino acid residue having a larger side chain volume, thereby creating a protuberance in the CH3 domain of the first subunit that can be positioned in a cavity in the CH3 domain of a second subunit, and in the CH3 domain of a second subunit of the Fc domain, an amino acid residue is replaced with an amino acid residue having a smaller side chain volume, thereby creating a cavity in the CH3 domain of the second subunit that can be positioned in the protuberance in the CH3 domain of the first subunit.

[0192] Preferably, the amino acid residue having a larger side chain volume is selected from the group consisting of arginine (R), phenylalanine (F), tyrosine (Y), and tryptophan (W).

[0193] Preferably, the amino acid residue having a smaller side chain volume is selected from the group consisting of alanine (A), serine (S), threonine (T) and valine (V).

[0194] The protrusions and cavities can be created by altering the nucleic acid encoding the polypeptide, for example, by site-directed mutagenesis or by peptide synthesis.

[0195] In specific embodiments, in the first subunit (of the CH3 domain) of the Fc domain (the "knob's" subunit), the threonine residue at position 366 is substituted with a tryptophan residue (T366W), and in the second subunit (of the CH3 domain) of the Fc domain (the "hole" subunit), the tyrosine residue at position 407 is substituted with a valine residue (Y407V). In some embodiments, the second subunit of the Fc domain further comprises a substitution of the threonine residue at position 366 with a serine residue (T366S) and a substitution of the leucine residue at position 368 with an alanine residue (L368A) (Kabat EU subscript numbering).

[0196] In yet a further embodiment, the first subunit of the Fc domain additionally has a substitution of a cysteine ​​residue for the serine residue at position 354 (S354C) or a cysteine ​​residue for the glutamic acid residue at position 356 (E356C) (particularly, the serine residue at position 354 is substituted with a cysteine ​​residue), and the second subunit of the Fc domain additionally has a substitution of a cysteine ​​residue for the tyrosine residue at position 349 (Y349C) (numbering according to the Kabat EU index). The introduction of these two cysteine ​​residues results in the formation of disulfide bridges between the two subunits of the Fc domain, further stabilizing the dimer (Carter, J Immunol Methods 248, 7-15 (2001)).

[0197] In a particular embodiment, the first subunit of the Fc domain comprises the amino acid substitutions S354C and T366W, and the second subunit of the Fc domain comprises the amino acid substitutions Y349C, T366S, L368A and Y407V (numbering according to the Kabat EU index).

[0198] Other techniques for CH3 modifications that enhance heterodimerization are contemplated as alternatives of the present invention and are described, for example, in WO 96 / 27011, WO 98 / 050431, EP 1870459, WO 2007 / 110205, WO 2007 / 147901, WO 2009 / 089004, WO 2010 / 129304, WO 2011 / 90754, WO 2011 / 143545, WO 2012 / 058768, WO 2013 / 157954, WO 2013 / 096291.

[0199] In some embodiments, the heterodimerization approach described in EP 1870459 is used instead. This technique is based on the introduction of oppositely charged amino acids at specific amino acid positions in the CH3 / CH3 domain interface between the two subunits of the Fc domain. A specific embodiment of the binding molecule of the present invention is the amino acid mutation R409D; K370E in one of the two CH3 domains (of the Fc domain) and the amino acid mutation D399K; E357K in the other CH3 domain of the Fc domain (numbering according to the Kabat EU index).

[0200] In some embodiments, a binding molecule of the invention comprises the amino acid mutation T366W in the CH3 domain of the first subunit of the Fc domain, and the amino acid mutations T366S, L368A, Y407V in the CH3 domain of the second subunit of the Fc domain, as well as the amino acid mutation R409D, K370E in the CH3 domain of the first subunit of the Fc domain, and the amino acid mutation D399K; E357K in the CH3 domain of the second subunit of the Fc domain (numbering according to EU suffix of Kabat).

[0201] In some embodiments, a binding molecule of the invention comprises the amino acid mutations S354C, T366W in the CH3 domain of the first subunit of the Fc domain and the amino acid mutations Y349C, T366S, L368A, Y407V in the CH3 domain of the second subunit of the Fc domain, or the binding molecule comprises the amino acid mutations Y349C, T366W in the CH3 domain of the first subunit of the Fc domain and the amino acid mutations S354C, T366S, L368A, Y407V in the CH3 domain of the second subunit of the Fc domain and further the amino acid mutation R409D, K370E in the CH3 domain of the first subunit of the Fc domain and the amino acid mutation D399K; E357K in the CH3 domain of the second subunit of the Fc domain (all numbered according to the Kabat EU index).

[0202] In some embodiments, the heterodimerization approach described in WO2013 / 157953 is used instead.In some embodiments, the first CH3 domain comprises the amino acid mutation T366K, and the second CH3 domain comprises the amino acid mutation L351D (Kabat EU suffix numbering).In further embodiments, the first CH3 domain comprises an additional amino acid mutation L351K.In further embodiments, the second CH3 domain further comprises an amino acid mutation selected from Y349E, Y349D and L368E (particularly L368E) (Kabat EU suffix numbering).

[0203] In some embodiments, the heterodimerization approach described in WO 2012 / 058768 is used instead. In some embodiments, the first CH3 domain comprises the amino acid mutations L351Y and Y407A, and the second CH3 domain comprises the amino acid mutations T366A and K409F. In further embodiments, the second CH3 domain comprises the amino acid mutations T411, D399, S400, F405, N390, or K392, e.g., a) T411N, T411R, T411Q, T411K, T411D, T411E, or T411W; b) D399R, D399W, D399Y, or D399K; c) S400E, S400D, S400F, or S400G. In a further embodiment, the first CH3 domain comprises an amino acid mutation selected from the group consisting of: d) F405I, F405M, F405T, F405S, F405V or F405W; e) N390R, N390K or N390D; and f) K392V, K392M, K392R, K392L, K392F or K392E (numbering according to EU suffix notation of Kabat). In a further embodiment, the first CH3 domain comprises the amino acid mutations L351Y and Y407A, and the second CH3 domain comprises the amino acid mutations T366V and K409F. In a further embodiment, the first CH3 domain comprises the amino acid mutation Y407A, and the second CH3 domain comprises the amino acid mutations T366A and K409F. In a further embodiment, the second CH3 domain further comprises the amino acid mutations K392E, T411E, D399R and S400R (numbering according to the EU suffix of Kabat).

[0204] In some embodiments, the heterodimerization approach described in WO 2011 / 143545 is alternatively used, e.g., involving amino acid modifications at positions selected from the group consisting of 368 and 409 (numbering according to the Kabat EU index).

[0205] In some embodiments, the heterodimerization approach described in WO 2011 / 090762, which also uses the knob-into-hole technique described above, is alternatively used. In some embodiments, the first CH3 domain comprises the amino acid mutation T366W and the second CH3 domain comprises the amino acid mutation Y407A. In some embodiments, the first CH3 domain comprises the amino acid mutation T366Y and the second CH3 domain comprises the amino acid mutation Y407T (numbering according to the EU index of Kabat).

[0206] In some embodiments, the binding molecule or its Fc domain is of the IgG2 subclass, and the heterodimerization approach described in WO 2010 / 129304 is alternatively used.

[0207] In an alternative embodiment, the modification that promotes association of the first and second subunits of the Fc domain comprises a modification that mediates an electrostatic steering effect, as described, for example, in PCT Application WO 2009 / 089004. Generally, this method involves replacing one or more amino acid residues at the interface of the two Fc domain subunits with charged amino acid residues, such that homodimer formation is electrostatically unfavorable, but heterodimerization is electrostatically favorable. In some such embodiments, the first CH3 domain comprises an amino acid substitution of K392 or N392 with a negatively charged amino acid (e.g., glutamic acid (E) or aspartic acid (D), particularly K392D or N392D), and the second CH3 domain comprises an amino acid substitution of D399, E356, D356, or E357 with a positively charged amino acid (e.g., lysine (K) or arginine (R), particularly D399K, E356K, D356K, or E357K, specifically D399K and E356K). In further embodiments, the first CH3 domain further comprises an amino acid substitution of K409 or R409 with a negatively charged amino acid (e.g., glutamic acid (E) or aspartic acid (D), particularly K409D or R409D). In a further aspect, the first CH3 domain additionally or alternatively comprises an amino acid substitution of K439 and / or K370 with a negatively charged amino acid (e.g., glutamic acid (E) or aspartic acid (D)) (all numbering according to the Kabat EU index).

[0208] In some embodiments, the heterodimerization approach described in WO 2007 / 147901 is used instead. In some embodiments, the first CH3 domain contains the amino acid mutations K253E, D282K, and K322D, and the second CH3 domain contains the amino acid mutations D239K, E240K, and K292D (numbering according to the EU index of Kabat).

[0209] In some embodiments, the heterodimerization approach described in WO 2007 / 110205 may alternatively be used.

[0210] In some embodiments, the first subunit of the Fc domain comprises the amino acid substitutions K392D and K409D, and the second subunit of the Fc domain comprises the amino acid substitutions D356K and D399K (numbering according to the Kabat EU index).

[0211] b) Fc domain modifications that reduce Fc receptor binding and / or effector function The Fc domain confers favorable pharmacokinetic properties to binding molecules, including a long serum half-life, which contributes to favorable accumulation in target tissues and favorable tissue-to-blood distribution ratios. However, at the same time, it can result in undesirable targeting of binding molecules to cells expressing Fc receptors rather than to preferred antigen-containing cells. Furthermore, coactivation of the Fc receptor signaling pathway can result in excessive activation of cytokine receptors and release of cytokines that can lead to severe side effects upon systemic administration. Activation of immune cells (bearing Fc receptors) other than T cells can even reduce the effectiveness of binding molecule pairs, for example, due to the potential destruction of T cells by NK cells.

[0212] Thus, in certain embodiments, the Fc domain of a binding molecule according to the invention exhibits reduced binding affinity to Fc receptors and / or reduced effector function compared to a native IgG1 Fc domain. In some such embodiments, the Fc domain (or a binding molecule comprising said Fc domain) exhibits less than 50%, particularly less than 20%, more particularly less than 10%, and most particularly less than 5% of the binding affinity to Fc receptors compared to a native IgG1 Fc domain (or a binding molecule comprising a native IgG1 Fc domain), and / or less than 50%, particularly less than 20%, more particularly less than 10%, and most particularly less than 5% of the effector function compared to a native IgG1 Fc domain (or a binding molecule comprising a native IgG1 Fc domain). In some embodiments, the Fc domain (or a binding molecule comprising said Fc domain) does not substantially bind to an Fc receptor and / or does not induce effector function. In certain embodiments, the Fc receptor is an Fcγ receptor. In some embodiments, the Fc receptor is a human Fc receptor. In some embodiments, the Fc receptor is an activating Fc receptor. In specific embodiments, the Fc receptor is an activating human Fcγ receptor, more specifically human FcγRIIIa, FcγRI, or FcγRIIa, most specifically human FcγRIIIa. In some embodiments, the effector function is one or more selected from the group consisting of CDC, ADCC, ADCP, and cytokine secretion. In specific embodiments, the effector function is ADCC. In some embodiments, the Fc domain exhibits substantially similar binding affinity to the neonatal Fc receptor (FcRn) compared to a native IgG1 Fc domain. Substantially similar binding to FcRn is achieved when the Fc domain (or a binding molecule comprising the Fc domain) exhibits more than about 70%, particularly more than about 80%, and more particularly more than about 90% of the binding affinity of a native IgG1 Fc domain (or a binding molecule comprising a native IgG1 Fc domain) to FcRn.

[0213] In certain embodiments, the Fc domain is engineered to have reduced binding affinity to an Fc receptor and / or reduced effector function compared to an unengineered Fc domain. In certain embodiments, the Fc domain of the binding molecule contains one or more amino acid mutations that reduce the binding affinity and / or effector function of the Fc domain to an Fc receptor. Typically, the same one or more amino acid mutations are present in each of the two subunits of the Fc domain. In some embodiments, the amino acid mutations reduce the binding affinity of the Fc domain to an Fc receptor. In some embodiments, the amino acid mutations reduce the binding affinity of the Fc domain to an Fc receptor by at least 2-fold, at least 5-fold, or at least 10-fold. In embodiments in which there are multiple amino acid mutations that reduce the binding affinity of the Fc domain to an Fc receptor, the combination of these amino acid mutations can reduce the binding affinity of the Fc domain to an Fc receptor by at least 10-fold, at least 20-fold, or at least 50-fold. In some embodiments, binding molecules comprising engineered Fc domains exhibit less than 20%, particularly less than 10%, and more particularly less than 5% of the binding affinity to Fc receptors compared to binding molecules comprising non-engineered Fc domains. In specific embodiments, the Fc receptor is an Fcγ receptor. In some embodiments, the Fc receptor is a human Fc receptor. In some embodiments, the Fc receptor is an activating Fc receptor. In specific embodiments, the Fc receptor is an activating human Fcγ receptor, more particularly human FcγRIIIa, FcγRI, or FcγRIIa, most particularly human FcγRIIIa. Preferably, binding of each of these receptors is reduced. In some embodiments, binding affinity to complement components (particularly binding affinity to C1q) is also reduced. In some embodiments, binding affinity to neonatal Fc receptor (FcRn) is not reduced. Substantially similar binding to FcRn, i.e., preservation of the binding affinity of the Fc domain to the receptor, is achieved when the Fc domain (or a binding molecule comprising the Fc domain) exhibits greater than about 70% of the binding affinity of the unengineered form of the Fc domain (or a binding molecule comprising the unengineered form of the Fc domain) to FcRn.The Fc domain, or a binding molecule of the present invention comprising the Fc domain, may exhibit greater than about 80%, or even greater than about 90%, of such affinity. In certain embodiments, the Fc domain of the binding molecule is engineered to have reduced effector function compared to an unengineered Fc domain. Reduced effector function may include, but is not limited to, one or more of: reduced complement-dependent cytotoxicity (CDC), reduced antibody-dependent cell-mediated cytotoxicity (ADCC), reduced antibody-dependent cellular phagocytosis (ADCP), reduced cytokine secretion, reduced immune complex-mediated antigen uptake by antigen-presenting cells, reduced binding to NK cells, reduced binding to macrophages, reduced binding to monocytes, reduced binding to polymorphonuclear cells, reduced direct signaling-induced apoptosis, reduced cross-linking with target-bound antibodies, reduced dendritic cell maturation, or reduced T cell priming. In some embodiments, the reduced effector function is one or more selected from the group consisting of reduced CDC, reduced ADCC, reduced ADCP, and reduced cytokine secretion. In certain embodiments, the reduced effector function is reduced ADCC, hi some embodiments, the reduced ADCC is less than 20% of the ADCC induced by a non-engineered Fc domain (or a binding molecule comprising a non-engineered Fc domain).

[0214] In some embodiments, the amino acid mutation that reduces the binding affinity of the Fc domain to an Fc receptor and / or the effector function is an amino acid substitution. In some embodiments, the Fc domain comprises an amino acid substitution at a position selected from the group of E233, L234, L235, N297, P331, and P329 (numbering according to the EU index of Kabat). In more specific embodiments, the Fc domain comprises an amino acid substitution at a position selected from the group of L234, L235, and P329 (numbering according to the EU index of Kabat). In some embodiments, the Fc domain comprises amino acid substitutions L234A and L235A (numbering according to the EU index of Kabat). In some such embodiments, the Fc domain is an IgG1 Fc domain, particularly a human IgG1 Fc domain. In some embodiments, the Fc domain comprises an amino acid substitution at position P329. In more specific embodiments, the amino acid substitution is P329A or P329G, particularly P329G (numbering according to the EU index of Kabat). In some embodiments, the Fc domain comprises an amino acid substitution at position P329 and an additional amino acid substitution at a position selected from E233, L234, L235, N297, and P331 (numbering according to EU index of Kabat). In more specific embodiments, the additional amino acid substitution is E233P, L234A, L235A, L235E, N297A, N297D, or P331S. In particular embodiments, the Fc domain comprises amino acid substitutions at positions P329, L234, and L235 (numbering according to EU index of Kabat). In even more particular embodiments, the Fc domain comprises the amino acid mutations L234A, L235A, and P329G ("P329G LALA," "PGLALA," or "LALAPG").Specifically, in certain embodiments, each subunit of the Fc domain comprises the amino acid substitutions L234A, L235A, and P329G (numbering according to the EU index of Kabat), i.e., in each of the first and second subunits of the Fc domain, the leucine residue at position 234 is substituted with an alanine residue (L234A), the leucine residue at position 235 is substituted with an alanine residue (L235A), and the proline residue at position 329 is substituted with a glycine residue (P329G) (numbering according to the EU index of Kabat).

[0215] In some such embodiments, the Fc domain is an IgG1 Fc domain, particularly a human IgG1 Fc domain. The "P329G LALA" combination of amino acid substitutions almost completely abolishes Fcγ receptor (and similarly, complement) binding of the human IgG1 Fc domain, as described in PCT Publication WO 2012 / 130831, the entire contents of which are incorporated herein by reference. WO 2012 / 130831 also describes methods for preparing such mutant Fc domains and determining their properties, such as Fc receptor binding or effector function.

[0216] IgG4 antibodies exhibit reduced binding affinity to Fc receptors and reduced effector function compared to IgG1 antibodies. Accordingly, in some embodiments, the Fc domain of a binding molecule of the present invention is an IgG4 Fc domain, particularly a human IgG4 Fc domain. In some embodiments, the IgG4 Fc domain comprises an amino acid substitution at position S228, specifically the amino acid substitution S228P (numbering according to EU index of Kabat). To further reduce its binding affinity to Fc receptors and / or its effector function, in some embodiments, the IgG4 Fc domain comprises an amino acid substitution at position L235, specifically the amino acid substitution L235E (numbering according to EU index of Kabat). In some embodiments, the IgG4 Fc domain comprises an amino acid substitution at position P329, specifically the amino acid substitution P329G (numbering according to EU index of Kabat). In certain embodiments, the IgG4 Fc domain comprises amino acid substitutions at positions S228, L235 and P329, specifically the amino acid substitutions S228P, L235E and P329G (numbering according to the Kabat EU index). Such IgG4 Fc domain mutants and their Fcγ receptor binding properties are described in PCT Publication No. WO 2012 / 130831, which is incorporated herein by reference in its entirety.

[0217] In particular embodiments, the Fc domain that exhibits reduced binding affinity to Fc receptors and / or reduced effector function compared to a native IgG1 Fc domain is a human IgG1 Fc domain comprising the amino acid substitutions L234A, L235A and optionally P329G, or a human IgG4 Fc domain comprising the amino acid substitutions S228P, L235E and optionally P329G (numbering according to the EU index of Kabat).

[0218] In certain embodiments, N-glycosylation of the Fc domain is eliminated, hi some such embodiments, the Fc domain comprises an amino acid mutation at position N297, particularly an amino acid substitution substituting asparagine with alanine (N297A) or aspartic acid (N297D) (numbering according to the EU index of Kabat).

[0219] In addition to the Fc domains described herein above and in PCT Publication WO 2012 / 130831, Fc domains with reduced Fc receptor binding and / or effector function also include those with one or more substitutions at Fc domain residues 238, 265, 269, 270, 297, 327, and 329 (U.S. Patent No. 6,737,056) (Kabat EU index numbering). Such Fc variants include Fc variants with substitutions at two or more of amino acid positions 265, 269, 270, 297, and 327, including the so-called "DANA" Fc variant in which residues 265 and 297 are substituted with alanine (U.S. Patent No. 7,332,581).

[0220] Variant Fc domains can be prepared by amino acid deletion, substitution, insertion, or modification using genetic or chemical methods well known in the art. Genetic methods may include site-directed mutagenesis of the encoding DNA sequence, PCR, gene synthesis, etc. Correct nucleotide changes can be confirmed, for example, by screening.

[0221] Binding to an Fc receptor can be readily determined, for example, by ELISA or by surface plasmon resonance (SPR) using standard equipment such as a BIAcore instrument (GE Healthcare) and an Fc receptor that can be obtained by recombinant expression. Alternatively, the binding affinity of an Fc domain or a binding molecule containing an Fc domain to an Fc receptor can be assessed using a cell line known to express a particular Fc receptor, such as human NK cells expressing the FcγIIIa receptor.

[0222] The effector function of Fc domain or binding molecules that contain Fc domain can be measured by methods known in the art.The example of the in vitro assay for evaluating the ADCC activity of target molecule is described in U.S. Patent No. 5,500,362, Hellstrom et al., Proc Natl Acad Sci USA 83,7059-7063(1986) and Hellstrom et al., Proc Natl Acad Sci USA 82,1499-1502(1985); U.S. Patent No. 5,821,337 Bruggemann et al., J Exp Med 166,1351-1361(1987). Alternatively, non-radioactive assay methods can be used (e.g., the ACTI® Non-Radioactive Cytotoxicity Assay for Flow Cytometry (CellTechnology, Inc. Mountain View, CA); and the CytoTox96® Non-Radioactive Cytotoxicity Assay (Promega, Madison, WI)). Useful effector cells for such assays include peripheral blood mononuclear cells (PBMCs) and natural killer (NK) cells. Alternatively, or additionally, ADCC activity of the molecule of interest may be assessed in vivo, for example, in an animal model such as that disclosed in Clynes et al., Proc Natl Acad Sci USA 95, 652-656 (1998).

[0223] In some embodiments, the binding of the Fc domain to complement components, particularly C1q, is reduced. Thus, in some embodiments in which the Fc domain is engineered to have reduced effector function, the reduced effector function includes reduced CDC. A C1q binding assay can be performed to determine whether the Fc domain or a binding molecule comprising an Fc domain can bind to C1q and therefore has CDC activity. See, for example, the C1q and C3c binding ELISAs in WO 2006 / 029879 and WO 2005 / 100402. To assess complement activation, a CDC assay may be performed (see, e.g., Gazzano-Santoro et al., J Immunol Methods 202, 163 (1996); Cragg et al., Blood 101, 1045-1052 (2003); and Cragg and Glennie, Blood 103, 2738-2743 (2004)).

[0224] Determination of FcRn binding and in vivo clearance / half-life can also be performed using methods known in the art (see, e.g., Petkova, SB et al., Int'l. Immunol. 18(12):1759-1769 (2006); WO 2013 / 120929).

[0225] Composition of binding molecules Binding molecules according to the invention may have a variety of molecular architectures, ie the domains of the binding molecule may be linked to each other in various ways.

[0226] In certain embodiments, the binding molecule comprises an Fc domain composed of a first subunit and a second subunit, wherein (i) the antigen-binding domain is fused at its C-terminus to the N-terminus of one of the Fc domain subunits, (ii) a portion of the effector domain is fused at its N-terminus to the C-terminus of one of the Fc domain subunits, and (iii) a complementarity domain is fused at its N-terminus to the C-terminus of the effector domain portion. In some such embodiments, the effector domain is an antigen-binding domain, particularly an anti-CD3 antigen-binding domain.

[0227] In some embodiments, the antigen-binding domain is a Fab molecule and is fused at the C-terminus of its heavy chain to the N-terminus of one of the Fc domain subunits. In some embodiments, a portion of the effector domain comprises (or consists of) a VH or VL and is fused at its N-terminus to the C-terminus of one of the Fc domain subunits. In some embodiments, a complementarity domain comprises (or consists of) a VH or VL and is fused at its N-terminus to the C-terminus of one of the effector domain subunits. In some such embodiments, the effector domain is an antigen-binding domain, particularly an anti-CD3 antigen-binding domain.

[0228] In some embodiments, The first binding molecule comprises: (i) a first antigen-binding domain and optionally a third antigen-binding domain; (ii) a first Fc domain composed of a first subunit and a second subunit; (iii) a first portion of an effector domain; and (iv) a first complementarity domain; (a) the first antigen-binding domain and the third antigen-binding domain (if present) are fused at their C-termini to the N-terminus of one of the subunits of the first Fc domain; (b) a first portion of the effector domain is fused at its N-terminus to the C-terminus of one of the subunits of the first Fc domain; (c) the first complementarity domain is fused at its N-terminus to the C-terminus of a first portion of the effector domain; The second binding molecule comprises: (i) a second antigen-binding domain and optionally a fourth antigen-binding domain; (ii) a second Fc domain composed of a first subunit and a second subunit; (iii) a second portion of the effector domain; and (iv) a second complementarity domain; (a) the second antigen-binding domain and the fourth antigen-binding domain (if present) are fused at their C-termini to the N-terminus of one of the subunits of the second Fc domain; (b) a second portion of the effector domain is fused at its N-terminus to the C-terminus of one of the subunits of the second Fc domain; (c) a second complementarity domain is fused at its N-terminus to the C-terminus of a second portion of said effector domain.

[0229] In some such embodiments, the effector domain is an antigen-binding domain, particularly an anti-CD3 antigen-binding domain.

[0230] In some embodiments, The first binding molecule comprises: (i) a first antigen-binding domain and optionally a third antigen-binding domain; (ii) a first Fc domain composed of a first subunit and a second subunit; (iii) a first portion of an effector domain; and (iv) a first complementarity domain; (a) the first antigen-binding domain and the third antigen-binding domain (if present) are fused at their C-termini to the N-terminus of one of the subunits of the first Fc domain; (b) a first part of the effector domain comprises (or consists of) a VH and is fused at its N-terminus to the C-terminus of one of the subunits of a first Fc domain; (c) the first complementarity domain comprises (or consists of) a VL and is fused at its N-terminus to the C-terminus of the first portion of the effector domain; The second binding molecule comprises: (i) a second antigen-binding domain and optionally a fourth antigen-binding domain; (ii) a second Fc domain composed of a first subunit and a second subunit; (iii) a second portion of the effector domain; and (iv) a second complementarity domain; (a) the second antigen-binding domain and the fourth antigen-binding domain (if present) are fused at their C-termini to the N-terminus of one of the subunits of the second Fc domain; (b) a second part of the effector domain comprises (or consists of) a VL and is fused at its N-terminus to the C-terminus of one of the subunits of a second Fc domain; (c) The second complementarity domain comprises (or consists of) a VH and is fused at its N-terminus to the C-terminus of a second part of the effector domain.

[0231] In some such embodiments, the effector domain is an anti-CD3 antigen-binding domain, particularly an anti-CD3 Fv molecule.

[0232] In some embodiments, The first binding molecule comprises: (i) a first antigen-binding domain and optionally a third antigen-binding domain; (ii) a first Fc domain composed of a first subunit and a second subunit; (iii) a first portion of an effector domain; and (iv) a first complementarity domain; (a) the first antigen-binding domain is a Fab molecule and is fused at its C-terminus to the N-terminus of the first subunit of the first Fc domain; (b) the third antigen-binding domain (if present) is a Fab molecule and is fused at its C-terminus to the N-terminus of the first subunit of the first Fc domain; (c) the first part of the effector domain comprises (or consists of) a VH and is fused at its N-terminus to the C-terminus of the first subunit or the second subunit of the first Fc domain; (d) the first complementarity domain comprises (or consists of) a VL and is fused at its N-terminus to the C-terminus of the first portion of the effector domain; The second binding molecule comprises: (i) a second antigen-binding domain and optionally a fourth antigen-binding domain; (ii) a second Fc domain composed of a first subunit and a second subunit; (iii) a second portion of the effector domain; and (iv) a second complementarity domain; (a) the second antigen-binding domain is a Fab molecule and is fused at its C-terminus to the N-terminus of the first subunit of the second Fc domain; (b) the fourth antigen-binding domain (if present) is a Fab molecule and is fused at its C-terminus to the N-terminus of the first subunit of the second Fc domain; (c) the second part of the effector domain comprises (or consists of) a VL and is fused at its N-terminus to the C-terminus of the first or second subunit of the second Fc domain; (d) a second complementarity domain comprising (or consisting of) a VH, fused at its N-terminus to the C-terminus of a second portion of the effector domain;

[0233] In some such embodiments, the effector domain is an anti-CD3 antigen-binding domain, particularly an anti-CD3 Fv molecule.

[0234] In some embodiments, the first binding molecule consists of a first antigen-binding domain, a first Fc domain, a first portion of the effector domain, a first complementary domain, and optionally one or more peptide linkers, and / or the second binding molecule consists of a second antigen-binding domain, a second Fc domain, a second portion of the effector domain, a second complementary domain, and optionally one or more peptide linkers. In some embodiments, the first binding molecule consists of a first antigen-binding domain, a third antigen-binding domain, a first Fc domain, a first portion of the effector domain, a first complementary domain, and optionally one or more peptide linkers, and / or the second binding molecule consists of a second antigen-binding domain, a fourth antigen-binding domain, a second Fc domain, a second portion of the effector domain, a second complementary domain, and optionally one or more peptide linkers.

[0235] Peptide Linker The domains of the binding molecules according to the invention (antigen binding domain, effector domain, complementarity domain, Fc domain...) can be fused to each other directly or via one or more peptide linkers.

[0236] Peptide linkers contain one or more amino acids, typically about 2 to 20 amino acids. Peptide linkers are known in the art and are described herein. Suitable non-immunogenic peptide linkers include, for example, (G4S) n , (SG4) n , G4(SG4) n or (G4S) n G5 peptide linkers are examples. "n" is generally an integer of 1 to 10, typically 2 to 4. In some embodiments, the peptide linker is at least 5 amino acids long, in some embodiments 5 to 100 amino acids long, and in further embodiments 10 to 50 amino acids long. In some embodiments, the peptide linker is a (GxS) n or (GxS) n G mwherein G=glycine, S=serine (x=3, n=3, 4, 5, or 6, and m=0, 1, 2, or 3) or (x=4, n=1, 2, 3, 4, or 5, and m=0, 1, 2, 3, 4, or 5); in some embodiments, x=4 and n=2 or 3; in further embodiments, x=4 and n=2; and in still further embodiments, x=4, n=1, and m=5. In some embodiments, the peptide linker is (G4S)2 (SEQ ID NO: 55). In other embodiments, the peptide linker is (G4S)G5. Furthermore, the linker may comprise (a portion of) an immunoglobulin hinge region. In particular, when a Fab molecule is fused to the N-terminus of an Fc domain subunit, it may be fused via an immunoglobulin hinge region or a portion thereof, with or without an additional peptide linker.

[0237] In some embodiments, the first antigen-binding domain and the third antigen-binding domain (if present) are each fused to one of the subunits of the first Fc domain via an immunoglobulin hinge region, and / or the second antigen-binding domain and the fourth antigen-binding domain (if present) are each fused to one of the subunits of the second Fc domain via an immunoglobulin hinge region.

[0238] In some embodiments, the first portion of the effector domain and the first Fc domain, and / or the second portion of the effector domain and the second Fc domain are fused via a peptide linker. In some embodiments, the first portion of the effector domain is fused at its N-terminus to the C-terminus of the first Fc domain subunit via a peptide linker, and / or the second portion of the effector domain is fused at its N-terminus to the C-terminus of the second Fc domain subunit via a peptide linker. An exemplary peptide linker suitable for fusing a portion of the effector domain to (the C-terminus of) an Fc domain subunit is (GS) (SEQ ID NO: 55). Thus, in some embodiments, a first portion of the effector domain is fused at its N-terminus to the C-terminus of a first Fc domain subunit via a peptide linker comprising the sequence (G4S)2 (SEQ ID NO: 55), and / or a second portion of the effector domain is fused at its N-terminus to the C-terminus of a second Fc domain subunit via a peptide linker comprising (G4S)2 (SEQ ID NO: 55). In particular embodiments, the peptide linker consists of the sequence (G4S)2 (SEQ ID NO: 55).

[0239] In some embodiments, the first portion of the effector domain and the first complementary domain, and / or the second portion of the effector domain and the second complementary domain are fused via a peptide linker. In some embodiments, the first portion of the effector domain is fused at its C-terminus to the N-terminus of the first complementary domain via a peptide linker, and / or the second portion of the effector domain is fused at its C-terminus to the N-terminus of the second complementary domain via a peptide linker. An exemplary peptide linker suitable for fusing a complementary domain to (the C-terminus of) a portion of an effector domain is (GS)GGSGG (SEQ ID NO: 56). Thus, in some embodiments, the first portion of the effector domain is fused at its C-terminus to the N-terminus of the first complementary domain via a peptide linker comprising the sequence of SEQ ID NO: 56, and / or the second portion of the effector domain is fused at its C-terminus to the N-terminus of the second complementary domain via a peptide linker comprising the sequence of SEQ ID NO: 56. In a particular embodiment, the peptide linker consists of the sequence of SEQ ID NO:56.

[0240] binding molecule The present invention also provides binding molecules forming part of a binding molecule pair of the invention, which may (unless the context dictates otherwise) incorporate any of the features described above and herein for binding molecule pairs, either alone or in combination.

[0241] Polynucleotides The present invention further provides isolated polynucleotides encoding a binding molecule pair of the present invention. The present invention also provides isolated polynucleotides encoding a binding molecule forming part of a binding molecule pair of the present invention. The isolated polynucleotides may be a single polynucleotide or multiple polynucleotides.

[0242] Polynucleotides encoding the binding molecules of the present invention can be expressed as a single polynucleotide encoding the entire binding molecule or binding molecule pair, or as multiple (e.g., two or more) co-expressed polynucleotides. Polypeptides encoded by co-expressed polynucleotides can associate, for example, by disulfide bonds or other means, to form a functional binding molecule. For example, the light chain portion of the antigen-binding domain can be encoded by a polynucleotide separate from the portion of the binding molecule comprising the heavy chain of the antigen-binding domain. When co-expressed, the heavy chain polypeptide combines with the light chain polypeptide to form the antigen-binding domain. In another example, the portion of the binding molecule consisting of one of the two Fc domain subunits and, optionally, one or more Fab molecules, can be encoded by a polynucleotide separate from the portion consisting of the other of the two Fc domain subunits and, optionally, one or more Fab molecules. When co-expressed, the Fc domain subunits associate to form the Fc domain.

[0243] In some embodiments, the isolated polynucleotide encodes an entire binding molecule pair or binding molecule of the invention as described herein, hi other embodiments, the isolated polynucleotide encodes a polypeptide comprised in a binding molecule pair or binding molecule of the invention as described herein.

[0244] In certain embodiments, the polynucleotide or nucleic acid is DNA. In other embodiments, the polynucleotide of the present invention is RNA, for example, in the form of messenger RNA (mRNA). The RNA of the present invention may be single-stranded or double-stranded.

[0245] Recombinant methods The binding molecules of the present invention can be obtained, for example, by solid peptide synthesis (e.g., Merrifield solid-phase synthesis) or recombinant production. For recombinant production, one or more polynucleotides encoding the binding molecules, for example, as described above, are isolated and inserted into one or more vectors for further cloning and / or expression in host cells. Such polynucleotides can be easily isolated and sequenced using conventional procedures. In one embodiment, vectors, particularly expression vectors, containing the polynucleotides of the present invention (i.e., a single polynucleotide or multiple polynucleotides) are provided. Methods well known to those skilled in the art can be used to construct expression vectors containing the coding sequence of the binding molecule along with appropriate transcriptional / translational control signals. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo recombination / genetic recombination. For example, Maniatis et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, NY (1989); and Ausubel et al., Current Protocols in Molecular Biology, Greene Publishing Associates and Wiley Interscience, NY (1989). The expression vector may be part of a plasmid, a virus, or a nucleic acid fragment. An expression vector comprises an expression cassette into which a polynucleotide encoding a binding molecule (i.e., a coding region) is cloned in operative linkage with a promoter and / or other transcriptional or translational control elements. As used herein, a "coding region" is a portion of a nucleic acid consisting of codons that are translated into amino acids. A "stop codon" (TAG, TGA, or TAA), although not translated into amino acids, may be considered part of the coding region, although any flanking sequences, if present, such as promoters, ribosome binding sites, transcription terminators, introns, 5' and 3' untranslated regions, etc., are not part of the coding region.Two or more coding regions may be present in a single polynucleotide construct, e.g., on a single vector, or in separate polynucleotide constructs, e.g., on separate (different) vectors. Furthermore, any vector may contain a single coding region or two or more coding regions; for example, the vectors of the present invention may encode one or more polypeptides, which are separated into final proteins by post- or co-translational proteolytic cleavage. Furthermore, the vectors, polynucleotides, or nucleic acids of the present invention may encode heterologous coding regions, fused or unfused to the polynucleotide encoding the binding molecule of the present invention, or its variant or derivative. Heterologous coding regions include, but are not limited to, specialized elements or motifs, such as secretory signal peptides or heterologous functional domains. Operable association refers to the association of a coding region for a gene product (e.g., a polypeptide) with one or more regulatory sequences in such a manner that expression of the gene product is under the influence or control of the regulatory sequences. Two DNA fragments (e.g., a polypeptide coding region and its associated promoter) are "operably associated" if the introduction of promoter function results in transcription of mRNA encoding the desired gene product, and if the nature of the linkage between the two DNA fragments does not interfere with the ability of the expression control sequences to direct expression of the gene product or to transcribe the DNA template. Thus, a promoter region is said to be operably linked to a nucleic acid encoding a polypeptide if the promoter is capable of effecting transcription of that nucleic acid. The promoter may be a cell-specific promoter that directs substantial transcription of the DNA only in predetermined cells. In addition to the promoter, other transcriptional regulatory elements, such as enhancers, operators, repressors, and transcription termination signals, may be operably associated with the polynucleotide to direct cell-specific transcription. Suitable promoters and other transcriptional control regions are disclosed herein. A variety of transcriptional control regions are known to those skilled in the art.These include, but are not limited to, transcriptional control regions that function in vertebrate cells, such as, but not limited to, promoter and enhancer segments from cytomegalovirus (e.g., in combination with the immediate early promoter, intron-A), Simian Virus 40 (e.g., the early promoter), and retroviruses (e.g., Rous sarcoma virus). Other transcriptional control regions include those derived from vertebrate genes, such as actin, heat shock proteins, bovine growth hormone, and rabbit β-globin, as well as other sequences capable of controlling gene expression in eukaryotic cells. Further suitable transcriptional control regions include tissue-specific promoters and enhancers, and inducible promoters (e.g., promoters induced by tetracycline). Similarly, various translational control elements are known to those skilled in the art. These include, but are not limited to, ribosome binding sites, translation initiation and termination codons, and elements derived from viral systems (particularly internal ribosome entry sites, or IRES, also known as CITE sequences). The expression cassette may also include other features, such as an origin of replication and / or chromosomal integration elements, such as the long terminal repeats (LTRs) of retroviruses or the inverted terminal repeats (ITRs) of adeno-associated viruses (AAV).

[0246] The polynucleotide and nucleic acid coding regions of the present invention may be associated with additional coding regions encoding secretory or signal peptides that direct the secretion of a polypeptide encoded by a polynucleotide of the present invention. For example, if secretion of a binding molecule is desired, DNA encoding a signal sequence can be placed upstream of the nucleic acid encoding the binding molecule or a fragment thereof. According to the signal hypothesis, proteins secreted by mammalian cells possess a signal peptide or secretory leader sequence that is cleaved from the mature protein upon initiation of transport of the growing protein chain across the rough endoplasmic reticulum. Those skilled in the art will recognize that polypeptides secreted by vertebrate cells typically possess a signal peptide fused to the N-terminus of the polypeptide, which is cleaved from the translated polypeptide to generate the secreted or "mature" form of the polypeptide. In certain embodiments, a native signal peptide, such as an immunoglobulin heavy or light chain signal peptide, or a functional derivative thereof that retains the ability to direct the secretion of a polypeptide operably linked thereto is used. Alternatively, a heterologous mammalian signal peptide or a functional derivative thereof can be used. For example, the wild-type leader sequence can be replaced with the leader sequence of human tissue plasminogen activator (TPA) or mouse β-glucuronidase.

[0247] DNA encoding short protein sequences that can be used to facilitate later purification (e.g., histidine tags) or to help label the binding molecule can be included internally or at the end of the binding molecule (fragment) encoding polynucleotide.

[0248] In some embodiments, host cells are provided that contain polynucleotides of the invention (i.e., a single polynucleotide or multiple polynucleotides). In particular embodiments, host cells are provided that contain vectors of the invention. The polynucleotides and vectors may incorporate any of the features described herein in connection with the polynucleotides and vectors, respectively, alone or in combination. In some such embodiments, the host cell contains one or more vectors (e.g., transformed or transfected as described below) that contain one or more polynucleotides encoding (portions of) the binding molecule pairs or binding molecules of the invention. As used herein, the term "host cell" refers to any type of cell line that can be engineered to produce the binding molecules of the invention or fragments thereof. Host cells suitable for supporting the replication and expression of binding molecules (e.g., antibodies) are well known in the art. Such cells can be transfected or transduced with a particular expression vector as needed, and large quantities of vector-containing cells can be grown to inoculate large-scale fermenters to obtain sufficient quantities of binding molecules for clinical use. Suitable host cells include prokaryotic microorganisms (e.g., Escherichia coli) or various eukaryotic cells, such as Chinese hamster ovary cells (CHO), insect cells, and the like. For example, polypeptides may be produced in bacteria, especially if glycosylation is not required. After expression, the polypeptide can be isolated from the bacterial cell paste in a soluble fraction and further purified. In addition to prokaryotes, eukaryotic microorganisms, such as filamentous fungi or yeast, are suitable cloning or expression hosts for polypeptide-encoding vectors, including fungal and yeast strains in which the glycosylation pathway has been "humanized" to produce polypeptides with partially or completely human glycosylation patterns. See Gerngross, Nat Biotech 22, 1409-1414 (2004) and Li et al., Nat Biotech 24, 210-215 (2006). Suitable host cells for the expression of (glycosylated) polypeptides are also derived from multicellular organisms (invertebrates and vertebrates). Examples of invertebrate cells include plant cells and insect cells.Numerous baculovirus strains have been identified and can be used in conjunction with insect cells, particularly for transfection of Spodoptera frugiperda cells. Plant cell cultures can also be used as hosts. See, for example, U.S. Patent Nos. 5,959,177, 6,040,498, 6,420,548, 7,125,978, and 6,417,429 (which describe the PLANTIBODIES™ technology for producing antibodies in transgenic plants). Vertebrate cells can also be used as hosts. For example, mammalian cell lines adapted to growth in suspension can be useful. Other examples of useful mammalian host cell lines are the monkey kidney CV1 line transformed by SV40 (COS-7); human embryonic kidney lines (e.g., 293 or 293T cells as described in Graham et al., J Gen Virol 36, 59 (1977)), baby hamster kidney cells (BHK), mouse Sertoli cells (e.g., TM4 cells as described in Mather, Biol Reprod 23, 243-251 (1980)), monkey kidney cells (CV1), African green monkey kidney cells (VERO-76), human cervical carcinoma cells (HELA), canine kidney cells (MDCK), buffalo rat liver cells (BRL3A), human lung cells (W138), human hepatocytes (HepG2), mouse mammary tumor cells (MMT060562), TRI cells (e.g., Mather et al., Annals of NY Acad Sci 383, 44-68 (1982), MRC5 cells, and FS4 cells. Other useful mammalian host cell lines include dhfr. -Examples include Chinese hamster ovary (CHO) cells, including CHO cells (Urlaub et al., Proc Natl Acad Sci USA 77, 4216 (1980)), and myeloma cell lines such as YO, NS0, P3X63, and Sp2 / 0. For a review of specific mammalian host cells suitable for protein production, see, for example, Yazaki and Wu, Methods in Molecular Biology, Vol. 248 (BKC Lo, ed., Humana Press, Totowa, NJ), pp. 255-268 (2003). Host cells include cultured cells, such as cultured mammalian cells, yeast cells, insect cells, bacterial cells, and plant cells, to name just a few, but also cells contained in transgenic animals, transgenic plants, or cultured plants or animal tissues. In some embodiments, the host cell is a eukaryotic cell, particularly a mammalian cell, such as a Chinese hamster ovary (CHO) cell, a human embryonic kidney (HEK) cell, or a lymphoid cell (e.g., a Y0, NS0, or Sp20 cell). In some embodiments, the host cell is not a cell within a human body.

[0249] Standard techniques for expressing foreign genes in these systems are known in the art. Cells that express a polypeptide containing either the heavy or light chain of an antigen-binding domain, such as an antibody, may also be engineered to express the other antibody chain, such that the expression product is an antibody having both a heavy and a light chain.

[0250] In one aspect, a method of producing a binding molecule pair according to the invention is provided, the method comprising culturing a host cell comprising a polynucleotide encoding a binding molecule pair provided herein under conditions suitable for expression of the binding molecule pair, and optionally recovering the binding molecule pair from the host cell (or host cell culture medium). Similarly, in one aspect, a method of producing a binding molecule according to the invention is provided, the method comprising culturing a host cell comprising a polynucleotide encoding a binding molecule provided herein under conditions suitable for expression of the binding molecule, and optionally recovering the binding molecule from the host cell (or host cell culture medium).

[0251] Binding molecules prepared as described herein can be purified by techniques known in the art, such as high-performance liquid chromatography, ion exchange chromatography, gel electrophoresis, affinity chromatography, and size exclusion chromatography. The actual conditions used to purify a particular protein will depend, in part, on factors such as net charge, hydrophobicity, and hydrophilicity, and will be apparent to those skilled in the art. For affinity chromatography purification, an antibody, ligand, receptor, or antigen to which the binding molecule binds can be used. For example, a matrix bearing Protein A or Protein G can be used for affinity chromatography purification of the binding molecules of the present invention. Sequential Protein A or G affinity chromatography and size exclusion chromatography can be used to isolate binding molecules essentially as described in the Examples. The purity of the binding molecule can be determined by any of a variety of well-known analytical methods, including gel electrophoresis, high-pressure liquid chromatography, and the like.

[0252] Compositions, Formulations and Routes of Administration In further aspects, the present invention provides pharmaceutical compositions comprising a binding molecule pair or binding molecule provided herein, e.g., for use in any of the following therapeutic methods. In some aspects, the pharmaceutical composition comprises a binding molecule pair or binding molecule according to the invention and a pharmaceutically acceptable carrier. In some aspects, the pharmaceutical composition comprises a binding molecule pair or binding molecule according to the invention and at least one additional therapeutic agent, e.g., as described below. Binding molecules forming part of a binding molecule pair can be included in one and the same pharmaceutical composition or in separate pharmaceutical compositions (i.e., each binding molecule forming part of a binding molecule pair is in a separate pharmaceutical composition). Typically, they are provided in separate pharmaceutical formulations to minimize the risk of binding between the first and second portions of the effector domain within the pharmaceutical composition. Thus, in certain aspects, the present invention provides a first pharmaceutical composition comprising a first binding molecule and a pharmaceutically acceptable carrier, and a second pharmaceutical composition comprising a second binding molecule and a pharmaceutically acceptable carrier. In other aspects, the present invention provides pharmaceutical compositions comprising first and second binding molecules and a pharmaceutically acceptable carrier.

[0253] Further provided is a method for producing a binding molecule pair or binding molecule of the invention in a form suitable for in vivo administration, comprising: (a) obtaining a binding molecule pair or binding molecule pair according to the invention; and (b) formulating the binding molecule pair or binding molecule with at least one pharmaceutically acceptable carrier, whereby a preparation of the binding molecule pair or binding molecule is formulated for in vivo administration.

[0254] The pharmaceutical compositions of the present invention comprise an effective amount of a binding molecule dissolved or dispersed in a pharmaceutically acceptable carrier. The phrase "pharmaceutically acceptable" refers to molecular entities and compositions that are generally non-toxic to recipients at the dosages and concentrations used, i.e., do not produce adverse allergic or other untoward reactions when administered to animals, e.g., humans, as appropriate. The preparation of pharmaceutical compositions containing a binding molecule and, optionally, additional active ingredients will be known to those skilled in the art in light of this disclosure, as exemplified by Remington's Pharmaceutical Sciences, 18th Edition, Mack Printing Company, 1990, incorporated herein by reference. Furthermore, for animal (e.g., human) administration, it will be understood that preparations should meet sterility, pyrogenicity, general safety, and purity standards as required by the FDA Office of Biological Standards or other national equivalents. Preferred compositions are lyophilized formulations or aqueous solutions. As used herein, "pharmaceutically acceptable carriers" include any and all solvents, buffers, dispersion media, coatings, surfactants, antioxidants, preservatives (e.g., antibacterial agents, antifungal agents), isotonicity agents, absorption delaying agents, salts, preservatives, antioxidants, proteins, drugs, drug stabilizers, polymers, gels, binders, excipients, disintegrants, lubricants, sweeteners, flavoring agents, dyes, and similar materials, and combinations thereof, as known to those skilled in the art (see, e.g., Remington's Pharmaceutical Sciences, 18th Ed., Mack Printing Company, 1990, pp. 1289-1329, incorporated herein by reference). Except insofar as any conventional carrier is incompatible with the active ingredient, its use in the pharmaceutical compositions is contemplated.

[0255] The binding molecule pairs or binding molecules of the present invention (and any additional therapeutic agents) can be administered by any suitable means, including parenteral, intrapulmonary, and intranasal, and, if desired for localized treatment, intralesional administration. Parenteral infusions include intramuscular, intravenous, intraarterial, intraperitoneal, or subcutaneous administration. Dosing can be by any suitable route, for example, injection, such as intravenous or subcutaneous injection, depending in part on whether the administration is short-term or long-term. In some embodiments, the binding molecules of the present invention are administered intravenously.

[0256] Parenteral compositions include those designed to be administered by injection, for example, subcutaneous, intradermal, intralesional, intravenous, intraarterial, intramuscular, intrathecal, or intraperitoneal injection. For injection, the binding molecules of the present invention can be formulated in aqueous solutions, particularly physiologically compatible buffers such as Hank's solution, Ringer's solution, or physiological saline buffer. The solutions may contain formulating agents such as suspending agents, stabilizing agents, and / or dispersing agents. Alternatively, the binding molecules may be in powder form for constitution with a suitable vehicle, such as sterile pyrogen-free water, before use. Sterile injectable solutions are prepared by incorporating the required amount of the binding molecules of the present invention in an appropriate solvent, along with various other ingredients listed below, as needed. Sterility can be easily achieved, for example, by filtration through a sterile filtration membrane. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle containing a basic dispersion medium and / or other ingredients. In the case of sterile powders for preparing sterile injectable solutions, suspensions, or emulsions, the preferred preparation method is vacuum drying or freeze-drying, which yields a powder of the active ingredient and any additional desired ingredients from a previously sterile-filtered liquid medium. The liquid medium should be appropriately buffered, if necessary, and the liquid diluent should first be rendered isotonic with sufficient saline or glucose prior to injection. The composition must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi. It will be appreciated that endotoxin contamination should be minimized to a safe level, e.g., less than 0.5 ng / mg protein.Suitable pharmaceutically acceptable carriers include, but are not limited to, buffers such as phosphate, citrate, and other organic acids; antioxidants including ascorbic acid and methionine; preservatives (e.g., octadecyldimethylbenzylammonium chloride; hexamethonium chloride; benzalkonium chloride; benzethonium chloride; phenol, butyl, or benzyl alcohol; alkyl parabens, such as methylparaben or propylparaben; catechol; resorcinol; cyclohexanol; 3-pentanol; and m-cresol); low molecular weight (less than about 10 residues) polypeptides; proteins Suspensions may include: substances such as serum albumin, gelatin, or immunoglobulin; hydrophilic polymers such as polyvinylpyrrolidone; amino acids such as glycine, glutamine, asparagine, histidine, arginine, or lysine; monosaccharides, disaccharides, and other carbohydrates (including glucose, mannose, or dextrin); chelating agents such as EDTA; sugars such as sucrose, mannitol, trehalose, or sorbitol; salt-forming counterions such as sodium; metal complexes (e.g., Zn-protein complexes); and / or nonionic surfactants such as polyethylene glycol (PEG). Aqueous injection suspensions may contain compounds that increase the viscosity of the suspension (e.g., sodium carboxymethylcellulose, sorbitol, dextran, etc.). Optionally, the suspension may also contain suitable stabilizers or agents that increase the solubility of the compound, allowing for the preparation of highly concentrated solutions. Additionally, suspensions of the active compound may be prepared as appropriate oil injection suspensions. Suitable lipophilic solvents or vehicles include fatty oils such as sesame oil, or synthetic fatty acid esters, such as ethyl oleate or triglycerides, or liposomes.

[0257] The active ingredient can also be incorporated into colloidal drug delivery systems (e.g., liposomes, albumin microspheres, microemulsions, nanoparticles, and nanocapsules), or into macroemulsions, for example, by coacervation techniques or microcapsules prepared by interfacial polymerization, such as hydroxymethylcellulose or gelatin microcapsules and poly(methyl methacrylate) microcapsules, respectively. Such techniques are disclosed in Remington's Pharmaceutical Sciences (18th Ed. Mack Printing Company, 1990). Sustained-release preparations may also be prepared. Suitable examples of sustained-release preparations include semipermeable matrices of solid hydrophobic polymers containing the polypeptide, which matrices are in the form of shaped articles, such as films or microcapsules. In certain embodiments, prolonged absorption of injectable compositions can be achieved by using agents that delay absorption, such as aluminum monostearate, gelatin, or combinations thereof, in the composition.

[0258] In addition to the above-mentioned compositions, binding molecules can also be formulated as depot preparations.Such long-acting preparations can be administered by implantation (for example, subcutaneous or intramuscular) or intramuscular injection.Therefore, for example, binding molecules can be formulated into suitable polymers or hydrophobic materials (for example, as emulsions in acceptable oils) or ion exchange resins, or as poorly soluble derivatives, for example, poorly soluble salts.

[0259] Pharmaceutical compositions containing the binding molecules of the present invention can be prepared by conventional mixing, dissolving, emulsifying, encapsulating, encapsulating or lyophilizing processes. Pharmaceutical compositions can be formulated in a conventional manner using one or more physiologically acceptable carriers, diluents, additives or auxiliary agents that facilitate the processing of proteins into pharmaceutically usable preparations. The appropriate formulation depends on the selected route of administration.

[0260] The binding molecule can be formulated in the composition in the form of a free acid or free base, neutral or salt. Pharmaceutically acceptable salts are salts that substantially retain the biological activity of the free acid or free base. These include acid addition salts, such as those formed with the free amino groups of the protein composition, or those formed with inorganic acids such as hydrochloric acid or phosphoric acid, or those formed with organic acids such as acetic acid, oxalic acid, tartaric acid or mandelic acid. In addition, salts formed with free carboxyl groups can be derived from inorganic bases such as sodium, potassium, ammonium, calcium or ferric hydroxide; or organic bases such as isopropylamine, trimethylamine, histidine or procaine. Pharmaceutical salts tend to be more soluble in aqueous and other protic solvents than the corresponding free base forms.

[0261] Therapeutic methods and compositions Any of the binding molecules provided herein can be used in methods of treatment. The binding molecules of the invention can be used as immunotherapeutic agents, for example, in the treatment of cancer.

[0262] For use in therapeutic methods, the binding molecules of the invention may be formulated, dosed, and administered in a manner consistent with good medical practice. Factors to consider in this regard include the particular disorder being treated, the particular mammal being treated, the clinical condition of the individual patient, the cause of the disorder, the site of delivery of the agent, the method of administration, the administration schedule, and other factors known to medical practitioners.

[0263] In the treatment method, a first binding molecule and a second binding molecule are used in combination. As used herein, "combination" (and its grammatical variants, such as "combined" or "combining") encompasses the combination of a first binding molecule and a second binding molecule, where the first binding molecule and the second binding molecule are in the same or different containers, in the same or different pharmaceutical preparations, administered together or separately, administered simultaneously or sequentially in any order, and administered by the same or different routes, provided that the first binding molecule and the second binding molecule can simultaneously bind to their target antigens on the surface of cells via their antigen-binding domains. For example, "combining" a first binding molecule and a second binding molecule can mean first administering the first binding molecule in a particular pharmaceutical preparation, followed by administering the second binding molecule in another pharmaceutical preparation, or vice versa.

[0264] The first binding molecule and the second binding molecule can be administered in any suitable manner known in the art. In some embodiments, the first binding molecule and the second binding molecule are administered sequentially (at different times). In other embodiments, the first binding molecule and the second binding molecule are administered simultaneously (simultaneously). In some embodiments, the first binding molecule and the second binding molecule are in separate compositions. In some embodiments, the first binding molecule and the second binding molecule are in the same composition.

[0265] In one embodiment, a binding molecule pair or binding molecule of the present invention is provided for use as a medicament. In a further embodiment, a binding molecule pair or binding molecule of the present invention is provided for use in treating a disease. In a particular embodiment, a binding molecule pair or binding molecule of the present invention is provided for use in a method of treatment. In one embodiment, the present invention provides a binding molecule pair or binding molecule of the present invention for use in treating a disease in an individual in need thereof. In one embodiment, the present invention provides a binding molecule pair for use in a method of treating an individual having a disease, comprising administering to the individual an effective amount of a binding molecule pair. In a particular embodiment, the disease is a proliferative disorder. In a particular embodiment, the disease is cancer. In some embodiments, the cancer is a solid tumor cancer. In some embodiments, the cancer is a cancer that expresses the target antigen of the binding molecule pair or binding molecule. In some embodiments (particularly when the antigen-binding domain of the first binding molecule and / or the second binding molecule can bind to HER2), the cancer is a HER2-expressing cancer. In a particular embodiment, the cancer is breast cancer. In certain embodiments, the method further comprises administering to the individual an effective amount of at least one additional therapeutic agent, e.g., an anti-cancer agent, when the disease being treated is cancer. In a further embodiment, the present invention provides a binding molecule pair of the present invention for use in inducing lysis of target cells, particularly cancer cells. In one embodiment, the present invention provides a binding molecule pair of the present invention for use in a method of inducing lysis of target cells, particularly cancer cells, in an individual, comprising administering an effective amount of the binding molecule pair to the individual and inducing lysis of the target cells. An "individual" according to any of the above embodiments is a mammal, preferably a human.

[0266] In a further aspect, the present invention provides the use of a binding molecule pair or binding molecule of the present invention in the manufacture or preparation of a medicament. In one aspect, the medicament is for treating a disease in an individual in need of treatment. In a further aspect, the medicament is for use in a method of treating a disease, comprising administering an effective amount of the medicament to an individual having the disease. In certain aspects, the disease is a proliferative disorder. In certain aspects, the disease is cancer. In some aspects, the cancer is a solid tumor cancer. In some aspects, the cancer is a cancer that expresses the target antigen of the binding molecule pair or binding molecule. In some aspects (particularly when the antigen-binding domain of the first binding molecule and / or the second binding molecule can bind to HER2), the cancer is a HER2-expressing cancer. In certain aspects, the cancer is breast cancer. In some aspects, the method further comprises administering to the individual an effective amount of at least one additional therapeutic agent, e.g., an anti-cancer agent, when the disease to be treated is cancer. In a further aspect, the medicament is for inducing lysis of target cells, particularly cancer cells. In a still further aspect, the medicament is for use in a method of inducing lysis of target cells, particularly cancer cells, in an individual, comprising administering to the individual an effective amount of the medicament to induce lysis of the target cells. The "individual" according to any of the above aspects may be a mammal, preferably a human.

[0267] In a further aspect, the present invention provides a method for treating a disease. In one aspect, the method comprises administering an effective amount of a binding molecule pair of the present invention to an individual having such a disease. In some embodiments, one or more compositions comprising a binding molecule pair of the present invention in a pharmaceutically acceptable form are administered to the individual. In certain embodiments, the disease is a proliferative disorder. In certain embodiments, the disease is cancer. In some embodiments, the cancer is a solid tumor cancer. In some embodiments, the cancer is a cancer that expresses the target antigen of the binding molecule pair or binding molecule. In some embodiments (particularly when the antigen-binding domain of the first binding molecule and / or the second binding molecule can bind to HER2), the cancer is a HER2-expressing cancer. In certain embodiments, the cancer is breast cancer. In certain embodiments, the method further comprises administering an effective amount of at least one additional therapeutic agent, e.g., an anti-cancer agent, to the individual when the disease to be treated is cancer. An "individual" according to any of the above aspects may be a mammal, preferably a human.

[0268] In a further aspect, the present invention provides a method for inducing lysis of a target cell. In some aspects, the target cell is a cell expressing the target antigen of the binding molecule pair or binding molecule. In some aspects (particularly when the antigen-binding domain of the first antigen-binding molecule and / or the second binding molecule can bind to HER2), the target cell is a HER2-expressing cell. In some aspects, the method comprises contacting the target cell with a binding molecule pair of the present invention in the presence of T cells, particularly cytotoxic T cells. In a further aspect, a method for inducing lysis of a target cell in an individual is provided. In some aspects, the target cell is a cell expressing the target antigen of the binding molecule pair or binding molecule. In some aspects (particularly when the antigen-binding domain of the first binding molecule and / or the second binding molecule can bind to HER2), the target cell is a HER2-expressing cell. In some such aspects, the method comprises administering an effective amount of a binding molecule pair of the present invention to an individual to induce lysis of the target cell. In one aspect, the "individual" is a human.

[0269] Those skilled in the art will readily recognize that in many cases, a binding molecule pair may not provide a treatment, but may only provide a partial benefit. In some embodiments, a physiological change that has some effect is also considered to be therapeutically beneficial. Thus, in some embodiments, the amount of a binding molecule pair that provides a physiological change is considered an "effective amount." The subject, patient, or individual in need of treatment is typically a mammal, more particularly, a human.

[0270] In some embodiments, an effective amount of a binding molecule pair of the invention is administered to an individual to treat a disease.

[0271] The appropriate dosage of the binding molecule pair of the present invention (when used alone or in combination with one or more other additional therapeutic agents) for the prevention or treatment of a disease depends on the type of disease being treated, the route of administration, the patient's weight, the type of binding molecule, the severity and course of the disease, whether the binding molecule pair is administered for prophylactic or therapeutic purposes, previous or concurrent therapeutic interventions, the patient's medical history and response to the binding molecule pair, and the discretion of the attending physician. The practitioner responsible for administration will, in any event, determine the concentration of active ingredient in the composition and the appropriate dose for each individual subject. Various dosing schedules are contemplated herein, including, but not limited to, single administration or multiple administrations over various time periods, bolus administration, and pulse infusion.

[0272] The binding molecule pair is suitably administered to the patient at one time or over a series of treatments. Depending on the type and severity of the disease, for example, about 1 μg / kg to 15 mg / kg (e.g., 0.1 mg / kg to 10 mg / kg) per binding molecule may be an initial candidate dosage for administration to the patient, whether by one or more separate administrations or by continuous infusion. Typical daily dosages may range from about 1 μg / kg to 100 mg / kg, depending on the factors mentioned above. For repeated administration over several days or longer, treatment is usually continued until a desired suppression of disease symptoms occurs, depending on the condition. Such doses may be administered intermittently, for example, weekly or every three weeks (e.g., so that the patient receives about two to about 20, or, for example, about six, doses of the binding molecule pair). An initial higher loading dose, followed by one or more lower doses, may be administered. However, other dosing regimens may also be useful. The progress of this therapy is easily monitored by conventional techniques and assays.

[0273] The binding molecule pairs of the present invention are generally used in an amount effective to achieve their intended purpose. For use in treating or preventing a disease state, the binding molecule pairs of the present invention or pharmaceutical compositions thereof are administered or applied in an effective amount.

[0274] For systemic administration, the effective dose can be estimated initially from in vitro assays, such as cell culture assays. The IC 50 A dose may also be formulated in animal models to achieve a circulating concentration range including 100 mg / kg / day. Such information can be used to more accurately determine useful doses in humans.

[0275] Initial dosages may also be estimated from in vivo data, eg, from animal models, using techniques well known in the art.

[0276] Dosage and administration intervals can be individually adjusted to provide plasma levels of the binding molecule sufficient to maintain therapeutic efficacy. Typical patient dosages for administration by injection range from about 0.1 to 50 mg / kg / day, typically about 0.5 to 1 mg / kg / day. Therapeutically effective plasma levels may be achieved by administering multiple doses each day. Plasma levels can be measured, for example, by HPLC.

[0277] An effective dose of the binding molecule pair of the present invention generally provides a therapeutic benefit without causing substantial toxicity. The toxicity and therapeutic efficacy of the binding molecule pair can be determined by standard pharmaceutical procedures in cell culture or experimental animals. Using cell culture assays and animal experiments, LD 50 (the dose that is lethal to 50% of the population) and ED 50 The dose ratio between toxic and therapeutic effects is the therapeutic index, which is the LD 50 / ED 50 Binding molecule pairs that exhibit large therapeutic indices are preferred. In some embodiments, binding molecule pairs according to the present invention exhibit high therapeutic indices. Data obtained from cell culture assays and animal studies can be used in formulating a dosage range appropriate for human use. Dosages are preferably administered at or above the ED 0 with little or no toxicity. 50 The blood concentration range includes: (a) a concentration of 100 mg / kg / day or more ...

[0278] The attending physician of a patient being treated with a binding molecule pair of the present invention will know how and when to terminate, interrupt, or adjust administration due to toxicity, organ dysfunction, etc. Conversely, the attending physician will also know to adjust treatment to higher levels if the clinical response is inadequate (without causing toxicity). The magnitude of an administered dose in the management of a target disorder will vary depending on the severity of the condition being treated, the route of administration, etc. The severity of the condition may, for example, be assessed, in part, by standard prognostic evaluation methods. Furthermore, the dose, and perhaps the frequency of administration, will also vary according to the age, weight, and response of the individual patient.

[0279] The binding molecules that form a binding molecule pair (i.e., a first binding molecule and a second binding molecule) may be administered in combination (where the binding molecules are contained in the same or separate compositions) or in separate administrations, where administration of the first binding molecule may occur before, simultaneously with, and / or after administration of the second binding molecule.

[0280] The binding molecule pairs of the present invention can be administered in combination with one or more other therapeutic agents. For example, the binding molecule pairs of the present invention can be co-administered with at least one additional therapeutic agent. The term "therapeutic agent" encompasses any agent administered to treat a condition or disease in an individual in need of such treatment. Such additional therapeutic agents can include any active ingredient appropriate for the particular disease being treated, preferably those with complementary activities that do not adversely affect each other. In certain embodiments, the additional therapeutic agent is an immunomodulator, a cytostatic agent, a cell adhesion inhibitor, a cytotoxic agent, an activator of cell apoptosis, or an agent that increases the sensitivity of cells to apoptosis inducers. In certain embodiments, the additional therapeutic agent is an anti-cancer agent, such as a microtubule-disrupting agent, an antimetabolite, a topoisomerase inhibitor, a DNA intercalator, an alkylating agent, hormone therapy, a kinase inhibitor, a receptor antagonist, an activator of tumor cell apoptosis, or an anti-angiogenic agent.

[0281] Such other agents are suitably present in combination in an amount effective for the intended purpose. The effective amount of such other agents depends on the amount of binding molecule pair used, the type of disorder or treatment, and other factors described above. Binding molecule pairs are generally used in the same dosages and by the same routes of administration as described herein, or at about 1 to 99% of the dosages described herein, or at any dosage, by any route determined empirically / clinically appropriate.

[0282] Such combination therapy as described above encompasses combined administration (where the two or more therapeutic agents are contained in the same or separate compositions) and separate administration, where administration of the binding molecule pair of the invention may occur before, simultaneously with, and / or after administration of the additional therapeutic agent and / or adjuvant. The binding molecule pair of the invention may also be used in combination with radiation therapy.

[0283] manufactured goods In another aspect of the present invention, an article of manufacture containing materials useful for the treatment, prevention, and / or diagnosis of the above-mentioned disorders (e.g., cancer) is provided. The article of manufacture comprises a container and a label or package insert affixed to or associated with the container. Suitable containers include, for example, bottles, vials, syringes, IV solution bags, and the like. The container may be formed from a variety of materials, such as glass or plastic. The container holds the composition by itself or in combination with another composition effective for treating, preventing, and / or diagnosing a condition, and may have a sterile access port (e.g., the container may be an intravenous solution bag or vial with a stopper pierceable by a hypodermic needle). In some embodiments, the composition comprises a binding molecule pair of the present invention. The article of manufacture in these embodiments may further comprise a label or package insert indicating that the composition can be used to treat a particular condition (e.g., cancer). In other embodiments, the article of manufacture comprises (a) a first container containing a composition, the composition comprising a first binding molecule, and (b) a second container containing a composition, the composition comprising a second binding molecule. These embodiments of the article of manufacture may further comprise a package insert indicating that the compositions can be used in combination to treat a particular condition (e.g., cancer).

[0284] In some aspects, the present invention provides an article of manufacture (kit) for treating a disease (e.g., cancer), comprising: (i) a container containing a pharmaceutical composition comprising a binding molecule pair of the present invention and an optional pharmaceutically acceptable carrier, and optionally (ii) a label or package insert containing instructions for using the pharmaceutical composition in treating the disease (e.g., cancer).

[0285] In another aspect, the present invention provides an article of manufacture (kit) for treating a disease (cancer), comprising: (i) a first container containing a first pharmaceutical composition comprising a first binding molecule of a binding molecule pair of the invention and an optional pharmaceutically acceptable carrier; (ii) a second container containing a second pharmaceutical composition comprising a second binding molecule of a binding molecule pair of the invention and an optional pharmaceutically acceptable carrier; and optionally (iii) a label or package insert containing instructions for using the first pharmaceutical composition and the second pharmaceutical composition in combination in treating the disease (cancer).

[0286] Alternatively, or additionally, the article of manufacture may further comprise a second (or third) container containing a pharmaceutically acceptable buffer, such as bacteriostatic water for injection (BWFI), phosphate-buffered saline, Ringer's solution, and dextrose solution. It may further include other materials desirable from a commercial and user standpoint, including other buffers, diluents, filters, needles, and syringes.

[0287] Methods for forming functional effector domains In a further aspect, the present invention provides a method for forming a functional effector domain, the method comprising contacting a binding molecule pair of the invention with a cell expressing said target antigens of the first and second antigen-binding domains under conditions that allow the first and second antigen-binding domains to bind to their target antigens on the surface of the cell. TIFF2025539760000002.tif252170TIFF2025539760000003.tif255170TIFF2025539760000004.tif25417 0TIFF2025539760000005.tif254170TIFF2025539760000006.tif254170TIFF2025539760000007.tif34170 [Brief explanation of the drawings]

[0288] [Figure 1]Schematic diagrams of exemplary SPLIT molecules according to the present invention. (A) A SPLIT molecule with bivalent binding to a target antigen and a non-complementary effector VL domain. (B) (A) A SPLIT molecule with bivalent binding to a target antigen and a non-complementary effector VH domain. (C) A SPLIT molecule with monovalent binding to a target antigen and a non-complementary effector VL domain. (D) A SPLIT molecule with monovalent binding to a target antigen and a non-complementary effector VH domain. (E) A SPLIT molecule with monovalent binding to a target antigen and a V-complementary effector VL domain. (F) A SPLIT molecule with monovalent binding to a target antigen and a V-complementary effector VH domain. Circles in the Fc region represent modifications that promote Fc heterodimerization, such as "knob-into-hole" modifications. [Figure 2] Various split anti-CD3 antibody molecules were tested in binding assays using Jurkat cells as target cells. Binding to Jurkat cells was determined by measuring median fluorescence intensity (MFI) by flow cytometry as described in the Methods section. MFI results are shown for the V9 binder (A), P035.093 binder (B), 40G5c binder (C), and C22 binder (D). Complementary molecules are indicated by gray circles, and non-complementary molecules are indicated by black circles. P1AF1375 + P1AF1376: Split molecule with non-complementary V9 binder. P1AF3870 + P1AF3871: Split molecule with complementary V9 binder. P1AF2484 + P1AF2678: Split molecule with non-complementary P035.093 binder. P1AF3868+P1AF3869: SPLIT molecule with V-complementary P035.093 binder. P1AA9518+P1AA9516: SPLIT molecule with non-complementary 40G5c binder. P1AF3865+P1AF3867: SPLIT molecule with V-complementary 40G5c binder. P1AF2678+P1AE6818: SPLIT molecule with non-complementary C22 binder. The format of all molecules is similar to that shown in Table 2. [Figure 3]Tumor cell killing of the ovarian adenocarcinoma cell line SKOV-3 (HER-2 positive) by CD3+ T cells from healthy donors was evaluated when treated with SPLIT molecules bearing various anti-CD3 binders. Tumor cell killing was measured after 48 hours by quantifying cell death using the CytotoxGlo kit (Promega). Cell death results are shown for the V9 binder (A), P035.093 binder (B), and 40G5c binder (C). Pairs are represented by filled symbols, symbols, and single prodrugs. P1AD4471: control molecule (non-SPLIT HER2 x CD3 bispecific antibody (with HER2 bivalent and CD3 monovalent binding)). P1AF3870 + P1AF3871: HER2-targeted SPLIT molecules bearing complementary V9 binders. P1AF3868+P1AF3869: HER2-targeted SPLIT molecule with complementary P035.093 binder. P1AE6814+P1AF2484: HER2-targeted SPLIT molecule with non-complementary P035.093 binder. P1AF3865+P1AF3867: HER2-targeted SPLIT molecule with complementary 40G5c binder. P1AD9224+P1AD9225: HER2-targeted SPLIT molecule with non-complementary 40G5c binder (having charged residues in the VH(Q39E) and VL(Q38K) domains as described hereinabove). The format of all SPLIT molecules is similar to the molecules shown in Table 2. [Figure 4]Tumor cell killing of the ovarian adenocarcinoma cell line SKOV-3 (HER-2 positive) by CD3+ T cells from healthy donors was evaluated when treated with SPLIT molecules containing the anti-CD3 binder P035.093. Tumor cell killing was measured after 48 hours by quantifying cell death using the CytotoxGlo kit (Promega). Cell death results are shown for non-complementary (A) and complementary (B) molecules. The positive control molecule (non-SPLIT HER2 x CD3 bispecific antibody) is shown as a filled square, the HER2+ HER2-producing pair is shown as a filled circle, and the HER2+ irrelevant binder is shown as an open symbol. P1AD4471: Control molecule (non-SPLIT HER2 x CD3 bispecific antibody). P1AE6814 + P1AF2484: HER2-targeted SPLIT molecule with the non-complementary P035.093 binder. P1AF2484 + P1AG7469: A SPLIT molecule with one HER2-targeted prodrug and one non-targeted (DP47) prodrug, and a non-complementary P035.093 binder. P1AF3868 + P1AF3869: A HER2-targeted SPLIT molecule with a complementary P035.093 binder. P1AF3869 + P1AG5786: A SPLIT molecule with one HER2-targeted prodrug and one non-targeted (DP47) prodrug, and a non-complementary P035.093 binder. The formats of all SPLIT molecules are similar to those shown in Table 2. [Figure 5]Tumor cell killing of the ovarian adenocarcinoma cell line SKOV-3 (HER-2 positive) by CD3+ T cells from healthy donors was evaluated. Tumor cell killing was measured after 48 hours by quantifying cell death using the CytotoxGlo kit (Promega). Cell death results are shown for non-complementary molecules containing the 40G5c binder (A) and C22 binder (B). The positive control molecule (non-SPLIT HER2xCD3 bispecific antibody) is shown as a filled square, the HER2+ HER2-producing pair is represented by a filled circle, and the HER2+ irrelevant binder is shown as an open symbol. P1AD4471: Control molecule (non-SPLIT HER2xCD3 bispecific antibody). P1AA9516+P1AA9518: HER2-targeted SPLIT molecules with the non-complementary 40G5c binder. P1AA9518 + P1AG7808: A SPLIT molecule with one HER2-targeted prodrug and one non-targeted (DP47) prodrug, and a non-complementary 40G5c binder. P1AE6814 + P1AE6818: A HER2-targeted SPLIT molecule with a non-complementary C22 binder. P1AE6818 + P1AG7469: A SPLIT molecule with one HER2-targeted prodrug and one non-targeted (DP47) prodrug, and a non-complementary C22 binder. The formats of all SPLIT molecules are similar to those shown in Table 2. [Figure 6]Tumor cell killing of the ovarian adenocarcinoma cell line SKOV-3 (highly HER-2 expressing cells) and the prostate cancer cell line LNCaP (lowly HER-2 expressing cells) by CD3+ T cells from healthy donors was evaluated. Tumor cell killing was measured after 48 hours by quantifying cell death using the CytotoxGlo kit (Promega). Cell death results are shown for the SKOV-3 cell line (A) and the LNCaP cell line (B) along with quantification of their respective antigen-binding sites (C). HER2+ HER2-producing pairs are represented by solid circles, and HER2+ unrelated binder pairs are represented by open symbols. P1AF3868+P1AF3869: HER2-targeted SPLIT molecule with the complementary P035.093 binder. P1AF3869+P1AG5786: A SPLIT molecule with one HER2-targeted prodrug and one non-targeted (DP47) prodrug, and the non-complementary P35.093 binder. The format of all molecules is similar to the molecules shown in Table 2. [Figure 7] Tumor cell killing of the ovarian adenocarcinoma cell line SKOV-3 (highly HER-2 expressing cells) and the prostate cancer cell line LNCaP (lowly HER-2 expressing cells) by CD3+ T cells from healthy donors was evaluated. Tumor cell killing was measured after 48 hours by quantifying cell death using the CytotoxGlo kit (Promega). Cell death results are shown for the SKOV-3 cell line (A) and the LNCaP cell line (B). Non-complementary pairs of various CD3 binders are shown as 40G5c (squares), C22 (circles), and P035.093 (diamonds). P1AA9518 + P1AA9516: HER2-targeted SPLIT molecule with the non-complementary 40G5c binder. P1AE6818 + P1AE6814: HER2-targeted SPLIT molecule with the non-complementary C22 binder. P1AF2484+P1AE6814: HER2-targeted SPLIT molecule with non-complementary P035.093 binder. The format of all molecules is similar to the molecules shown in Table 2. [Figure 8]Ex vivo analysis of human T cells from humanized mice. Mice were injected with equimolar doses of SPLIT molecules, and blood was collected and analyzed 24 hours after treatment to assess the formation of circulating target-independent CD3 binders. T cell-binding molecules were measured by flow cytometry using a PE-labeled anti-human IgG, Fc-specific secondary antibody. Median fluorescence intensity values ​​are shown for CD4+ T cells (A) and CD8+ T cells (B) from blood of animals treated with non-complementary and complementary P035.093 compounds. P1AE6814 + P1AF2484: HER2-targeted SPLIT molecule with non-complementary P035.093 binder. P1AF3868 + P1AF3869: HER2-targeted SPLIT molecule with complementary P035.093 binder. The format of all molecules is similar to that shown in Table 2. [Figure 9] Ex vivo analysis of human T cells from humanized mice. Mice were injected with equimolar doses of SPLIT molecules, and blood was collected and analyzed 24 hours after treatment to assess the formation of target-independent CD3 binders in the circulation. T cell-binding molecules were measured by flow cytometry using a PE-labeled anti-human IgG, Fc-specific secondary antibody. Median fluorescence intensity is shown for CD4+ T cells (A) and CD8+ T cells (B) from the blood of animals treated with non-complementary and complementary V9 compounds. P1AF1375 + P1AF1376: Tumor antigen-targeted SPLIT molecule with non-complementary V9 binder. P1AF3870 + P1AF3871: HER2-targeted SPLIT molecule with complementary V9 binder. The format of all molecules is similar to that shown in Table 2. [Figure 10]Ex vivo analysis of human T cells from humanized mice. Mice were injected with equimolar doses of SPLIT molecules, and blood was collected and analyzed 24 hours after treatment to assess the formation of target-independent CD3 binders in the circulation. T cell-binding molecules were measured by flow cytometry using a PE-labeled anti-human IgG, an Fc-specific secondary antibody. Median fluorescence intensity is shown for CD4+ T cells (A) and CD8+ T cells (B) from the blood of animals treated with non-complementary compounds based on C22 and 40G5c as CD3 binders. P1AF6814 + P1AF6818: HER2-targeted SPLIT molecules with non-complementary C22 binders. P1AF9516 + P1AF9518: HER2-targeted SPLIT molecules with non-complementary 40G5c binders. The format of all molecules is similar to that shown in Table 2. [Example]

[0289] The following are examples of methods and compositions of the present invention. Given the general description provided above, it will be understood that various other embodiments may be practiced.

[0290] Example 1. Generation of SPLIT molecules with or without V complementarity. 1.1 Construction of expression plasmids for SPLIT molecules For the expression of the SPLIT constructs reported herein, a transcription unit containing the following functional elements was used: - the immediate early enhancer and promoter from human cytomegalovirus (P-CMV) containing intron A, - human heavy chain immunoglobulin 5' untranslated region (5'UTR), - mouse immunoglobulin heavy chain signal sequence, - a nucleic acid encoding each of the fusion polypeptides, and - Bovine growth hormone polyadenylation sequence (BGH pA).

[0291] In addition to the expression unit / cassette containing the desired gene, a basic / standard mammalian expression plasmid is - the origin of replication from the vector pUC18, allowing replication of this plasmid in E. coli, and -Contains the beta-lactamase gene that confers ampicillin resistance to E. coli.

[0292] 1.2 Expression of SPLIT molecules Transient expression of SPLIT molecules was performed in suspension-adapted HEK293F (FreeStyle 293-F cells; Invitrogen) cells or Expi293 (Expi293F™ cells; Thermofisher Scientific) using Transfection Reagent 293-free (Novagen) or ExpiFectamine™ 293 Transfection Kit (ExpiFectamine™ 293 reagent, ExpiFectamine™ 293 transfection enhancers 1 and 2).

[0293] After thawing in 125 ml shake flasks (incubated / shaken at 37°C, 7% CO2, 85% humidity, 135 rpm), cells were passaged at least four times (30 ml volume) by dilution. Cells were cultured at 3 x 10 in a 250 ml volume. 5 After 3 days, cells were split and placed in 1 L shake flasks at 1.5 x 10 cells / ml in a 250 ml volume. 6 ~7×10 5 The cells were freshly seeded at a density of approximately 1.4–3.0 × 10 cells / ml. 24 hours after transfection, the cells were transfected to a density of approximately 1.4–3.0 × 10 cells / ml. 6 The cell density was measured in cells / ml.

[0294] Prior to transfection, 250 μg of plasmid DNA was diluted to a final volume of 10 ml with preheated (water bath; 37°C) Opti-MEM (Gibco). The solution was gently mixed and incubated at room temperature for a maximum of 5 minutes. For transfection with ExpiFectamine™, 675 μl of ExpiFectamine™ 293 reagent was added to 12.5 ml of OptiMEM solution and incubated in a separate tube for 5 minutes. The two solutions were then combined, gently mixed, and incubated at room temperature for 15–20 minutes. The complete mixture was then added to a 1 L shake flask containing 250 ml of Expi293 cell culture. For 293-free transfection, 333.3 μl of 293-free transfection reagent was added directly to the DNA-OptiMEM solution. The resulting solution was gently mixed and incubated at room temperature for 15–20 minutes. The entire mixture was added to a 1 L shake flask containing 250 ml of HEK293F cell culture.

[0295] Incubation was carried out by shaking the flasks at 37°C, 7% CO , 85% humidity, and 135 rpm for 6–7 days.

[0296] The supernatant was collected by a first centrifugation step at 2,000 rpm for 10 min at 4° C. The supernatant was then transferred to a new centrifuge flask and centrifuged a second time at 4,000 rpm for 20 min at 4° C. The cell-free supernatant was then filtered through a 0.22 μm bottle-top filter and stored in a freezer (−20° C.).

[0297] 1.3 Purification of SPLIT molecules The culture supernatant containing SPLIT molecules was filtered and purified by two chromatography steps. Antibodies were captured by affinity chromatography using a HiTrap MabSelectSuRe (GE Healthcare) column equilibrated with PBS (1 mM KH2PO4, 10 mM Na2HPO4, 137 mM NaCl, 2.7 mM KCl), pH 7.4. Unbound proteins were removed by washing with the equilibration buffer, and SPLIT molecules were recovered in 50 mM citrate buffer (pH 2.8) and neutralized to pH 6.0 with 1 M Tris base (pH 9.0) immediately after elution. Alternatively, SPLIT molecules were eluted from the MabSelectSuRe column with 100 mM acetic acid, pH 3.0, and adjusted to pH 5.5. Protein samples recovered from affinity chromatography were analyzed by analytical SEC, and depending on the impurity profile, additional purification steps were performed. For additional purification steps, either an ion-exchange column (POROS XS or POROS HS50), a hydroxyapatite column (MacroPrep CHT Type I, BioRad), or a hydrophobic interaction chromatography (HIC) column (TSkgel Ether-5PW, Tosoh Bioscience, Griesheim, Germany) was used. For hydroxyapatite chromatography, the MabSelectSuRe eluate was diluted (1:5 vol / vol) with 10 mM sodium citrate, pH 5.0, and either adjusted to pH 7.5 with 2 M Tris / HCl, pH 9.0, or dialyzed against 50 mM acetate buffer, pH 7.5. After adding a small amount of calcium chloride, the protein solution was loaded onto a MacroPrep column equilibrated with 25 mM HEPES, 5 mM NaHPO, 50 mM NaCl, 0.1 mM CaCl, 100 mM MES, pH 6.8, and eluted with a gradient of the same buffer containing a final concentration of 1500 mM NaCl. The SPLIT protein was purified by POROS XS ion exchange chromatography in 20 mM His / His-HCl buffer at pH 5.5 with a salt gradient of 0 to 550 mM NaCl.Alternatively, VL fusion proteins were best prepared using 40 mM Na acetate buffer with a combined pH / NaCl gradient of 4.5-5 and 125 mM to 600 mM NaCl. VH fusion proteins were best prepared on a POROS XS column in 20 mM Na phosphate buffer, pH 5.5, with a salt gradient of 5-500 mM NaCl. For hydrophobic interaction chromatography, 40 mM sodium acetate buffer (pH 5.5) contained 1.5 M (NH4)2SO4, and elution was achieved with a shallow gradient of 50 column volumes toward no salt content. Size-exclusion chromatography on a Superdex 200™ column (GE Healthcare) was used as the polishing step in all cases. Size-exclusion chromatography was performed in 20 mM histidine buffer, 0.14 M NaCl, pH 6.0. Finally, the SPLIT molecule-containing solution was concentrated with an Ultrafree-CL centrifugal filter unit equipped with a Biomax-SK membrane (Millipore, Billerica, MA) and stored at −80°C.

[0298] 1.4 Mass analysis of SPLIT molecules PNGase F was obtained from Roche Diagnostics GmbH (14.3 U / μl; solution in sodium phosphate, EDTA, and glycerol). The protease, which specifically cleaves in the hinge region of IgG antibodies, was freshly reconstituted from a lyophilizate before digestion.

[0299] Enzymatic deglycosylation by PNGase F 50 μg of SPLIT molecules were diluted to a final concentration of 0.5 mg / ml in 10 mM sodium phosphate buffer (pH 7.1) and deglycosylated with 1 μl of PNGase F at 37° C. for 16 hours.

[0300] ESI-QTOF mass spectrometry The digested samples were then analyzed by LC-MS. Liquid chromatography was performed on a Waters Acquity UPLC (Waters) equipped with a reversed-phase C18 column (Agilent PLRP-S column, 2.1 × 150 mm, 8 μm, 1000 Å (Agilent, catalog number: PL1912-3802)). The aqueous mobile phase (mobile phase A) contained 0.1% (v / v) formic acid (FA) in HPLC-grade water. The organic mobile phase (mobile phase B) contained 0.1% FA in acetonitrile. The gradients utilized in this experiment are plotted in Table 1. [Table 1]

[0301] Further chromatographic settings were as follows: -Flow rate: 0.6mL / min -Column oven temperature: 75℃ -Injection volume: 8μL

[0302] The UPLC was coupled to an ESI-QTOF MS instrument (maXis 4G UHR-QTOF MS system (Bruker Daltonik)). Calibration was performed using sodium iodide. Data acquisition was performed for the digested SPLIT molecules from m / z 800 to 4000 (isCID: 85 eV). Raw mass spectra were evaluated and converted to individual relative molar masses. Deconvoluted mass spectra were generated using proprietary software to visualize the results.

[0303] The SPLIT molecules that were generated are shown in Table 2. The molecules either contained a complementary domain or did not. [Table 2]

[0304] The purification yields of various SPLIT molecules are shown in Table 3. [Table 3]

[0305] In the case of the CD3 binder V9, complementation of the single VH and VL domains with the corresponding DP47 V domains significantly improved the production yield of the SPLIT constructs, specifically improving the purification yield of the V9 SPLIT VH construct from 0.8 mg / L for the non-complementary SPLIT construct P1AE6819 to 20.8 mg / L for the DP47-complementary construct P1AF3870.

[0306] V complementation of the CD3 binder P035.093 with the cognate V domain of DP47 significantly improved the stability and developability of the SPLIT P035.093 construct, although it somewhat reduced the purification yield (see Example 2).

[0307] In the case of 40G5c, V-complementation with DP47 significantly improved the purification procedure, as the non-complementary SPLIT constructs P1AA9518 and P1AA9516 could only be purified in sufficient yield via hydroxyapatite chromatography, whereas the V-complementary constructs P1AF3865 and P1AF3867 did not require this delicate purification method to obtain sufficient quantities.

[0308] Example 2. Developability of SPLIT molecules. 2.1 Physicochemical characterization Apparent hydrophobicity Apparent hydrophobicity was assessed by measuring retention time on a hydrophobic HPLC column in comparison with known highly and less hydrophobic standard molecules.

[0309] Penalty kick prediction Interactions with immobilized FcRn and heparin on specific HPLC columns were evaluated, and the corresponding retention times were compared to established thresholds based on known molecules with good and poor PK.

[0310] Thermal stability and aggregation tendency Molecules are exposed to a controlled gradient of increasing temperature to determine their tendency to aggregate (T by SLS). agg ) was measured.

[0311] The results for apparent hydrophobicity, PK prediction, thermal stability and aggregation tendency are shown in Table 4 below.

[0312] 2.2 Early stability assessment Storage Molecules were stored under conditions that mimicked both physiological and shelf life conditions, and were stored for extended periods at relevant temperatures (physiological and stress conditions). Subsequent analysis focused on changes observed in the stored samples compared to untreated controls.

[0313] analysis Molecular aggregation was assessed using SE-HPLC setup with conditions appropriate for the molecule being evaluated. Fragmentation of molecules was assessed using capillary gel electrophoresis. Functional integrity of molecules was assessed with binding assays specific for the molecule's target.

[0314] The results of the early stability evaluation are shown in Table 5 below. [Table 4] [Table 5]

[0315] The thermostability and stress resistance data of the constructs with the SPLIT CD3 domain of 40G5c already met the criteria for acceptance of the developability analysis for the non-complementary SPLIT constructs P1AA9518 and P1AA9516 without the need for V complementation.

[0316] V complementation of the P035.093 SPLIT constructs (P1AF3868 and P1AF3869) with DP47 significantly improved developability properties compared to the non-complementary SPLIT constructs P1AE6814 and P1AF2484, particularly with respect to apparent hydrophobicity and stress stability as determined by SEC.

[0317] Example 3. Functional characterization of SPLIT molecules. 3.1 Method Flow cytometry binding to human T cells The binding of SPLIT molecules to human T cells was evaluated. A molecular titration in RPMI + 10% FBS was added to the cells at an equimolar ratio for the complementary VH / VL pair of the SPLIT molecule. The plate was incubated in the dark at 4°C for 60 minutes. To remove unbound molecules, the plate was washed twice with cold PBS, and the cell pellet was resuspended in cold FACS buffer containing PE-conjugated anti-human Fc gamma-specific goat IgG F(ab)2 fragment (Jackson ImmunoResearch) and Zombie Aqua (Biolegend) as secondary detection antibodies to identify live cells. The plate was incubated in the dark at 4°C for 30 minutes, washed twice with cold PBS, and resuspended in FACS buffer.

[0318] Cells were acquired using a FORTESSA flow cytometry device (Becton Dickinson) and an automated HTS plate processing system.

[0319] Data were analyzed using FlowJo v10.8.1 for PC (FlowJo LLC), Microsoft Excel (Microsoft Office Standard 2016), and TIBCO SpotFire v10.10.4 (TIBCO Software Inc).

[0320] T cell-mediated tumor cell killing The molecules were tested in a tumor cell killing assay using freshly isolated human CD3+ T cells co-incubated with target cells. Tumor cell lysis was measured by quantification of extracellular protease activity released into the supernatant by apoptotic or necrotic cells as described below.

[0321] Target cells were detached using trypsin (Gibco), washed once with PBS, and resuspended at a density of 0.2 mio cells / ml in growth medium (RPMI 1640 (Gibco)) containing 10% FBS and 1% GlutaMax (Gibco). 100 μl of the cell suspension (containing 20,000 cells) was seeded into a 96-well flat-bottom plate and incubated overnight at 37°C in an incubator. After Ficoll isolation from healthy donor blood, CD3+ T cells were isolated from PBMCs and viability was confirmed. Antibodies were diluted in assay medium at the indicated concentrations, and the molecules were added to the target cells.

[0322] Assay medium was added to the appropriate wells to equalize the volume in each well. Isolated CD3+ T cells were resuspended at a density of 4 mio cells / ml and 50 μl was added per well, yielding 200,000 cells / well (E:T 10:1). For measurement of apoptotic cell protease release, CD3+ effector and target cells were co-incubated as a negative control.

[0323] Assays were incubated at 37°C, 5% CO2 for a total of 72 hours. Measurements of dead cell protease activity were performed 24, 48, and / or 72 hours after assay initiation, as indicated in the figures. For this, the CytoTox-Glo™ Cytotoxicity Assay (Promega, no. G9291) was allowed to warm to room temperature before measurement. For analysis, 50 μl of supernatant per well was transferred to a 96-well white flat-bottom plate. 25 μl of substrate was then added to each well, and after 15 minutes of incubation at room temperature, luminescence was measured using a Perkin Elmer EnVision® 2104 instrument.

[0324] Quantification of antigen density on target cells Flow cytometry estimation of antibody bound per cell was performed using BD Quantibrite™ beads (Becton Dickinson #340495) and a monoclonal PE-conjugated antibody targeting human CD340 (HER2) (Biolegend #324406). 200,000 cells of each cell line were harvested and washed twice with 200 μl of FACS buffer. Antibody dilutions were prepared in FACS buffer (1:100). Cells were centrifuged, resuspended in 100 μl of antibody solution, and then incubated at 4°C for 30 minutes. 100 μl of FACS buffer was added before centrifugation, and the cells were washed twice with 200 μl of FACS buffer. Samples were then acquired using a BD LSRFortessa™ Cell Analyzer and BD Quantibrite™ Beads. Calculations and analysis were performed according to the manufacturer's protocol. Data were analyzed using FlowJo v10.8.1 for PC (FlowJo LLC), Microsoft Excel (Microsoft Office Standard 2016), and TIBCO SpotFire v10.10.4 (TIBCO Software Inc).

[0325] Ex vivo analysis of human T cells from treated humanized mice In one study, NSG-huNSG mice were supplied by Charles River and implanted in-house with human stem cells according to internal protocols. 3 When the mice reached a size of 100 μL, they were intravenously injected with complementary VH / VL paired SPLIT molecules. VH and VL molecule administration was separated by approximately 20 minutes, with doses of 1.53–1.71 mg / kg SPLIT molecules in 100 μL of vehicle buffer (20 mM histidine, 140 mM NaCl, pH 6.0), for a total of 200 μL injected. As a negative control, 200 μL of vehicle buffer was injected. In a separate experiment, CD34-transplanted NSG mice were supplied by Jackson Laboratories and injected with complementary VH / VL paired SPLIT molecules (2.5–2.8 mg / kg per molecule in 100 μL) as described above.

[0326] In both studies, blood was collected from 3-4 mice 24 hours after treatment administration and collected in heparin tubes. Red blood cell lysis was performed on the blood samples, and single cells were stained for human CD45, CD8a, CD25, CD69, CD4, and PE-conjugated anti-human IgG (for detection of therapeutic molecules bound to CD4+ and CD8+ T cells). Samples were acquired on a BD LSRFortessa cell analyzer.

[0327] 3.2 Results As shown in Figure 2, without complementation, a molecular pair composed of SPLIT V9 (A) and SPLIT P035.093 (B) assembled and bound to CD3 Jurkat T cells in the absence of target cells, whereas the CD3 binders 40G5c (C) and C22 (D) did not. Importantly, complementation of split P035.093 (A) and split V9 (B) inhibited assembly on T cells in the absence of target tumor cells.

[0328] As shown in Figure 3, treatment with the SPLIT pair (HER2 + HER2) and the positive control (non-SPLIT HER2 x CD3 T cell bispecific antibody (with bivalent HER2 binding and monovalent CD3 binding)) resulted in potent T cell-mediated killing of SKOV-3 tumor cells after 48 hours of co-incubation, whereas the single prodrug showed no activity. Although SPLIT complementation reduced potency compared to the non-complementary pair, this result indicates that the tested SPLIT pairs, including the complementary pair, can induce T cell-mediated tumor cell killing when both molecules bind to target cells and assemble into an active CD3 binder. This also indicates that the prodrugs remain inactive in the absence of their cognate partners.

[0329] The split pair and the non-complementary CD3 binder P035.093 pair (Figure 4(A)) demonstrate that T cell-mediated tumor cell killing occurs not only with the productive pair, but also with the HER2-unrelated binder pair. This result indicates that only one of the two molecules can bind to tumor cells, but that assembly of an active complex can occur with the non-complementary P035.093. This undesired assembly can be prevented by complementation, as shown in Figure 4(B). Indeed, the HER2+HER2-complementary pair induces T cell-mediated tumor cell killing, whereas the complementary HER2+ unrelated binder pair does not. These results demonstrate the importance of P035.093's complementarity in restricting activity to only target cells bound by both molecules, although this comes at the expense of slightly reduced potency.

[0330] As shown in Figure 5(A), split pairing with the non-complementary CD3 binder 40G5c demonstrates that T cell-mediated tumor cell killing occurs not only with the productive pair (HER2+HER2) but also with the pairing with an unrelated HER2 binder, albeit to a limited extent at high concentrations. This result suggests that active complex assembly can occur with the non-complementary 40G5c pair when both molecules can bind to tumor cells, but functional complex assembly occurs to a much lesser extent when only one molecule can bind to target cells. Similar results can be observed in Figure 5(B) for the CD3 binder C22. Overall, the data in Figures 4 and 5 demonstrate that functional complex assembly can vary depending on the VH and VL modules and whether complementation is used. This provides engineering opportunities to tune the forces driving complex assembly.

[0331] As shown in Figure 6(A), SPLIT pairing with the complementary CD3-binding agent P035.093 confirms T cell-mediated target cell killing activity when both molecules can bind to the target cell, but no killing is observed when only one molecule can bind. As shown in Figure 6(B,C), assembly of an active complex does not occur at target cells with low antigen density. Indeed, this adds an additional requirement for productive assembly of an active complex. Not only must both molecules bind to the target cell, but the antigen density must be sufficient to trigger T cell activation and target cell killing. Because relevant targets for T cell redirection in oncology are frequently observed in healthy tissues, albeit at lower levels than in tumor cells, the density threshold requirement may provide an additional safety benefit by limiting activity to cells expressing low levels of both targets.

[0332] As shown in Figure 7(B), non-complementary SPLIT molecules, despite being active against high target expressing cells, may or may not be active against low target expressing cells, depending on their CD3 binder (Figure 7(A)).

[0333] Ex vivo analysis of human T cells from humanized mice sampled 24 hours after treatment with SPLIT pairs shows in Figure 8 that non-complementary pairs using P035.093 as a CD3 binder can assemble in the absence of binding to the target pair and bind to CD3 on CD4+ T cells (A) and CD8+ T cells (B) circulating in the blood. Complementarity of the P035.093 CD3 module inhibits pair assembly on circulating T cells.

[0334] Ex vivo analysis of human T cells from humanized mice sampled 24 hours after treatment with SPLIT pairs shows that non-complementary pairs using V9 as a CD3 binder can assemble in the absence of binding to their target pair and bind to CD3 on circulating CD4+ T cells (A) and CD8+ T cells (B), as shown in Figure 9. Complementation of the V9 CD3 module strongly reduced pair assembly on circulating T cells. Overall, Figures 8 and 9 demonstrate that complementation of SPLIT CD3 improves the behavior of circulating SPLIT compounds, limiting assembly on T cells when the molecules are not bound to their target pair.

[0335] Ex vivo analysis of human T cells from humanized mice sampled 24 hours after treatment with SPLIT pairs indicates that other CD3-binding agents (e.g., 40G5c and C22) do not require complementation to prevent binding to CD3 on circulating CD4+ T cells (A) and CD8+ T cells (B), as shown in Figure 10.

[0336] The foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, but these descriptions and examples should not be construed as limiting the scope of the invention. The disclosures of all patent and scientific literature cited herein are expressly incorporated by reference in their entirety.

Claims

1. (a) a first binding molecule comprising (i) a first antigen-binding domain capable of binding to a target antigen, (ii) a first portion of an effector domain, and (iii) a first complementarity domain capable of binding to the first portion of the effector domain; and (b) a binding molecule pair comprising (i) a second antigen-binding domain capable of binding to a target antigen, (ii) a second portion of an effector domain, and (iii) a second binding molecule comprising a second complementarity domain capable of binding to said second portion of said effector domain; the first and second portions of the effector domain are capable of binding to each other to form a functional effector domain when the first antigen-binding domain and the second antigen-binding domain bind to a target antigen on a cell surface; a binding molecule pair, wherein the first complementarity domain and the second complementarity domain are bound to the first and second portions of the effector domain, respectively, and the first and second portions of the effector domain are not bound to each other.

2. The binding molecule pair of claim 1 , wherein the effector domain is an antigen-binding domain.

3. The binding molecule pair of claim 1 or 2, wherein the effector domain is an anti-CD3 antigen-binding domain.

4. The binding molecule pair according to any one of claims 1 to 3, wherein the functional effector domain is capable of binding to an antigen.

5. The binding molecule pair according to claim 4, wherein the antigen is a T cell antigen, in particular an activated T cell antigen.

6. 6. A binding molecule pair according to claim 4 or 5, wherein the antigen is CD3, in particular CD3ε.

7. The binding molecule pair of any one of claims 1 to 6, wherein the first portion of the effector domain comprises a heavy chain variable region (VH) and the second portion of the effector domain comprises a light chain variable region (VL).

8. The binding molecule pair of claim 7, wherein the VH comprises a heavy chain complementarity determining region (HCDR) 1 of SEQ ID NO: 15, a HCDR2 of SEQ ID NO: 16, and a HCDR3 of SEQ ID NO: 17, and the VL comprises a light chain complementarity determining region (LCDR) 1 of SEQ ID NO: 19, a LCDR2 of SEQ ID NO: 20, and a LCDR3 of SEQ ID NO:

21.

9. The binding molecule pair of claim 8, wherein the VH comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 18, and / or the VL comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO:

22.

10. The binding molecule pair of claim 7, wherein the VH comprises a heavy chain complementarity determining region (HCDR) 1 of SEQ ID NO: 23, a HCDR2 of SEQ ID NO: 24, and a HCDR3 of SEQ ID NO: 25, and the VL comprises a light chain complementarity determining region (LCDR) 1 of SEQ ID NO: 27, a LCDR2 of SEQ ID NO: 28, and a LCDR3 of SEQ ID NO:

29.

11. The binding molecule pair of claim 10, wherein the VH comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 26, and / or the VL comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO:

30.

12. The binding molecule pair of claim 7, wherein the VH comprises a heavy chain complementarity determining region (HCDR) 1 of SEQ ID NO: 31, a HCDR2 of SEQ ID NO: 32, and a HCDR3 of SEQ ID NO: 33, and the VL comprises a light chain complementarity determining region (LCDR) 1 of SEQ ID NO: 35, a LCDR2 of SEQ ID NO: 36, and a LCDR3 of SEQ ID NO:

37.

13. The binding molecule pair of claim 12, wherein the VH comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 34, and / or the VL comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO:

38.

14. The binding molecule pair of claim 7, wherein the VH comprises a heavy chain complementarity determining region (HCDR) 1 of SEQ ID NO: 23, a HCDR2 of SEQ ID NO: 24, and a HCDR3 of SEQ ID NO: 60, and the VL comprises a light chain complementarity determining region (LCDR) 1 of SEQ ID NO: 27, a LCDR2 of SEQ ID NO: 28, and a LCDR3 of SEQ ID NO:

29.

15. The binding molecule pair of claim 14, wherein the VH comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 61, and / or the VL comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO:

30.

16. The binding molecule pair according to any one of claims 1 to 15, wherein the first complementarity domain and the second complementarity domain are incapable of forming a functional effector domain with a part of the effector domain.

17. 17. The binding molecule pair of any one of claims 1 to 16, wherein the first complementary domain comprises a VL and the second complementary domain comprises a VH.

18. The binding molecule pair of claim 17, wherein the VH and the VL are non-antigen binding.

19. The binding molecule pair of claim 17 or 18, wherein the VH comprises a heavy chain complementarity determining region (HCDR) 1 of SEQ ID NO: 47, a HCDR2 of SEQ ID NO: 48, and a HCDR3 of SEQ ID NO: 49, and the VL comprises a light chain complementarity determining region (LCDR) 1 of SEQ ID NO: 51, a LCDR2 of SEQ ID NO: 52, and a LCDR3 of SEQ ID NO:

53.

20. 20. The binding molecule pair of claim 19, wherein the VH comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 50, and / or the VL comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO:

54.

21. 21. The binding molecule pair of any one of claims 1 to 20, wherein the first portion of the effector domain comprises a first VH, the first complementary domain comprises a first VL, the second portion of the effector domain comprises a second VL, and the second complementary domain comprises a second VH.

22. 22. The binding molecule pair of claim 21, wherein each of the second VH and the first VL and / or each of the first VH and the second VL, particularly each of the second VH and the first VL, comprises an amino acid substitution in which an amino acid residue is replaced with a charged replacement amino acid residue, and (i) the substituted amino acid residue in the VH and the VL has an opposite charge, or (ii) the substituted amino acid residue in the VH and the VL has the same charge.

23. 23. The binding molecule pair of any one of claims 1 to 22, wherein the first binding molecule comprises a third antigen-binding domain capable of binding to a target antigen, and / or the second binding molecule comprises a fourth antigen-binding domain capable of binding to a target antigen.

24. The binding molecule pair of any one of claims 1 to 23, wherein the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and / or the fourth antigen-binding domain (if present) is an antigen-binding domain selected from the group consisting of an Fv molecule, an scFv molecule, an Fab molecule, and a single-domain antibody.

25. 25. The binding molecule pair of any one of claims 1 to 24, wherein the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present) and / or the fourth antigen-binding domain (if present) are Fab molecules.

26. The binding molecule pair of any one of claims 1 to 25, wherein the first antigen-binding domain and the second antigen-binding domain bind to the same target antigen.

27. The binding molecule pair of any one of claims 1 to 26, wherein the first antigen-binding domain and the second antigen-binding domain bind to the same target antigen, the third antigen-binding domain (if present) and the fourth antigen-binding domain (if present) bind to the same target antigen, and the target antigen bound by the first antigen-binding domain and the second antigen-binding domain is different from the target antigen bound by the third antigen-binding domain (if present) and the fourth antigen-binding domain (if present).

28. The binding molecule pair of any one of claims 1 to 25, wherein the first antigen-binding domain and the second antigen-binding domain bind to different target antigens.

29. 29. The binding molecule pair of any one of claims 1 to 25 or 28, wherein the first antigen-binding domain and the third antigen-binding domain (if present) bind to the same target antigen, the second antigen-binding domain and the fourth antigen-binding domain (if present) bind to the same target antigen, and the target antigen bound by the first antigen-binding domain and the third antigen-binding domain (if present) is different from the target antigen bound by the second antigen-binding domain and the fourth antigen-binding domain (if present).

30. 30. The binding molecule pair of any one of claims 1 to 29, wherein the target antigens of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) are tumor antigens.

31. The binding molecule pair of any one of claims 1 to 30, wherein the target antigen of the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present), and the fourth antigen-binding domain (if present) is HER2.

32. 32. The binding molecule pair of any one of claims 1 to 31, wherein the first antigen-binding domain, the second antigen-binding domain, the third antigen-binding domain (if present) and / or the fourth antigen-binding domain (if present) comprise a heavy chain variable region (VH) and a light chain variable region (VL).

33. The binding molecule pair of claim 32, wherein the VH comprises a heavy chain complementarity determining region (HCDR) 1 of SEQ ID NO: 39, a HCDR2 of SEQ ID NO: 40, and a HCDR3 of SEQ ID NO: 41, and the VL comprises a light chain complementarity determining region (LCDR) 1 of SEQ ID NO: 43, a LCDR2 of SEQ ID NO: 44, and a LCDR3 of SEQ ID NO:

45.

34. The binding molecule pair of claim 33, wherein the VH comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO: 42, and / or the VL comprises an amino acid sequence that is at least about 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequence of SEQ ID NO:

46.

35. 35. The binding molecule pair of any one of claims 1 to 34, wherein the first binding molecule comprises a first Fc domain composed of a first subunit and a second subunit, and / or the second binding molecule comprises a second Fc domain composed of a first subunit and a second subunit.

36. The Fc domain is IgG, particularly IgG １ 36. The binding molecule pair of claim 35, which is an Fc domain.

37. 37. The binding molecule pair of claim 35 or 36, wherein the Fc domain is a human Fc domain.

38. The Fc domain is human IgG １ The binding molecule pair according to any one of claims 35 to 37, which is an Fc domain.

39. 39. The binding molecule pair of any one of claims 35 to 38, wherein the Fc domain comprises a modification that promotes binding of the first subunit and the second subunit of the Fc domain.

40. 40. The binding molecule pair of any one of claims 35 to 39, wherein the Fc domain comprises one or more amino acid substitutions that reduce binding to an Fc receptor and / or effector function.

41. the first binding molecule comprising: (i) a first antigen-binding domain and optionally a third antigen-binding domain; (ii) an Fc domain composed of a first subunit and a second subunit; (iii) a first portion of an effector domain; and (iv) a first complementarity domain; (a) the first antigen-binding domain and the third antigen-binding domain (if present) are fused at their C-termini to the N-terminus of one of the subunits of the Fc domain; (b) the first portion of the effector domain is fused at its N-terminus to the C-terminus of one of the subunits of the Fc domain; (c) the first complementarity domain is fused at its N-terminus to the C-terminus of the first portion of the effector domain; the second binding molecule comprising: (i) a second antigen-binding domain and optionally a fourth antigen-binding domain; (ii) an Fc domain composed of a first subunit and a second subunit; (iii) a second portion of the effector domain; and (iv) a second complementarity domain; (a) the second antigen-binding domain and the fourth antigen-binding domain (if present) are fused at their C-termini to the N-terminus of one of the subunits of the Fc domain; (b) the second portion of the effector domain is fused at its N-terminus to the C-terminus of one of the subunits of the Fc domain; (c) the second complementarity domain is fused at its N-terminus to the C-terminus of the second part of the effector domain.

42. 42. The binding molecule pair of any one of claims 1 to 41, wherein the first part of the effector domain and the first complementary domain, and / or the second part of the effector domain and the second complementary domain are fused via a peptide linker.

43. 43. The binding molecule pair of claim 42, wherein the peptide linker comprises the sequence of SEQ ID NO:

56.

44. A binding molecule forming part of a binding molecule pair according to any one of claims 1 to 43.

45. An isolated polynucleotide encoding a pair of binding molecules according to any one of claims 1 to 43 or a binding molecule according to claim 44.

46. 46. ​​A host cell comprising the isolated polynucleotide of claim 45.

47. 47. A method for producing a binding molecule (pair), comprising: (a) culturing the host cell of claim 46 under conditions suitable for expression of the binding molecule (pair), and optionally (b) recovering the binding molecule (pair).

48. A pharmaceutical composition comprising the binding molecule pair of any one of claims 1 to 43 or the binding molecule of claim 44, and a pharmaceutically acceptable carrier.

49. A binding molecule pair according to any one of claims 1 to 43, a binding molecule according to claim 44, or a pharmaceutical composition according to claim 48 for use as a medicament.

50. A binding molecule pair according to any one of claims 1 to 43, a binding molecule according to claim 44, or a pharmaceutical composition according to claim 48 for use in the treatment of a disease.

51. 51. The binding molecule pair, binding molecule or pharmaceutical composition for use according to claim 50, wherein the disease is cancer.

52. 49. Use of a binding molecule pair according to any one of claims 1 to 43, a binding molecule according to claim 44, or a pharmaceutical composition according to claim 48 in the manufacture of a medicament.

53. 49. Use of a binding molecule pair according to any one of claims 1 to 43, a binding molecule according to claim 44, or a pharmaceutical composition according to claim 48 in the manufacture of a medicament for treating a disease.

54. 54. The use of claim 53, wherein the disease is cancer.

55. 44. A method of treating a disease in an individual, comprising administering to said individual an effective amount of a binding molecule pair according to any one of claims 1 to 43.

56. 56. The method of claim 55, wherein the disease is cancer.

57. 10. An article of manufacture (kit) for the treatment of a disease, comprising: (i) a container containing a pharmaceutical composition comprising the binding molecule pair of any one of claims 1 to 43 and an optional pharmaceutically acceptable carrier; and optionally (ii) a label or package insert containing instructions for using the pharmaceutical composition in the treatment of said disease.

58. 10. An article of manufacture (kit) for treating a disease, comprising: (i) a first container containing a first pharmaceutical composition comprising the first binding molecule of the binding molecule pair of any one of claims 1 to 43 and an optional pharmaceutically acceptable carrier; (ii) a second container containing a second pharmaceutical composition comprising the second binding molecule of the binding molecule pair of any one of claims 1 to 43 and an optional pharmaceutically acceptable carrier; and optionally (iii) a label or package insert containing instructions for using the first pharmaceutical composition and the second pharmaceutical composition in combination in treating the disease.

59. 59. The article of manufacture of claim 57 or 58, wherein the disease is cancer.

60. 44. A method for forming a functional effector domain, comprising contacting the binding molecule pair of any one of claims 1 to 43 with a cell expressing the target antigens of the first and second antigen-binding domains under conditions that allow the first and second antigen-binding domains to bind to their target antigens on the surface of the cell.

61. 10. The invention as hereinbefore described.

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