Anti-B7-H3 monoclonal antibodies and methods of use thereof

Abstract

Provided herein are agents such as antibodies, antibody-drug conjugates, or chimeric antigen receptors that target B7-H3. Provided are methods for treating cancer, including administering an effective amount of a B7-H3 targeting agent to a patient in need thereof. If the cancer expresses an increased level of B7-H3, the patient can be selected for treatment.

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority to U.S. Provisional Application No. 62 / 936,783, filed November 18, 2019, the entire contents of which are incorporated herein by reference.

[0002] Reference to sequence listing This application has been submitted via EFS-Web in ASCII format and contains a Sequence Listing, which is incorporated herein by reference in its entirety. The ASCII copy was created on November 4, 2020, is named UTFCP1481WO_ST25.txt, and is 6.9 kilobytes in size. [Background technology]

[0003] 1. Field The present invention relates generally to the fields of medicine, immunology, and cancer biology, and more particularly to antibodies that target B7-H3 and methods of their use.

[0004] 2. Description of Related Art Harnessing the host immune system through attenuation of endogenous immune checkpoints on effector T cells has resulted in dramatic and durable tumor responses in selected patients with solid tumors (Sharma et al., 2011). Antibodies that block co-inhibitory T cell signals, such as those targeting CTLA-4, PD-1, and PD-L1, have demonstrated objective response rates of 10–30% in patients with a variety of otherwise fatal solid tumors, including metastatic melanoma, RCC, NSCLC, and ovarian cancer, and many promising immune checkpoint therapies (ICTs) are currently underway as monotherapy and in combination clinical trials. However, significant toxic side effects remain, and many patients are resistant to ICTs. Therefore, novel approaches to block immune checkpoints for therapeutic purposes are needed. Summary of the Invention

[0005] overview In one embodiment, a monoclonal antibody or antibody fragment is provided herein, wherein the antibody or antibody fragment comprises a heavy chain variable region (VH) comprising the VHCDR1, VHCDR2, and VHCDR3 amino acid sequences from the MIL33B antibody, and a light chain variable region (VL) comprising the VLCDR1, VLCDR2, and VLCDR3 amino acid sequences from the MIL33B antibody.

[0006] In some embodiments, the antibody or antibody fragment comprises a heavy chain variable region (VH) comprising the VHCDR1, VHCDR2, and VHCDR3 amino acid sequences derived from SEQ ID NO: 7, and a light chain variable region (VL) comprising the VLCDR1, VLCDR2, and VLCDR3 amino acid sequences derived from SEQ ID NO: 8. In some embodiments, the antibody or antibody fragment is capable of binding to B7-H3.

[0007] In some embodiments, the antibody or antibody fragment comprises a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 1, the VHCDR2 amino acid sequence of SEQ ID NO: 2, and the VHCDR3 amino acid sequence of SEQ ID NO: 3, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 4, the VLCDR2 amino acid sequence of SEQ ID NO: 5, and the VLCDR3 amino acid sequence of SEQ ID NO: 6.

[0008] In some embodiments, the antibody or antibody fragment comprises a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 11, the VHCDR2 amino acid sequence of SEQ ID NO: 12, and the VHCDR3 amino acid sequence of SEQ ID NO: 13, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 14, the VLCDR2 amino acid sequence of SEQ ID NO: 15, and the VLCDR3 amino acid sequence of SEQ ID NO: 16.

[0009] In some embodiments, the antibody or antibody fragment comprises a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 17, the VHCDR2 amino acid sequence of SEQ ID NO: 18, and the VHCDR3 amino acid sequence of SEQ ID NO: 19, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 20, the VLCDR2 amino acid sequence of SEQ ID NO: 21, and the VLCDR3 amino acid sequence of SEQ ID NO: 6.

[0010] In some embodiments, the antibody or antibody fragment comprises a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 17, the VHCDR2 amino acid sequence of SEQ ID NO: 18, and the VHCDR3 amino acid sequence of SEQ ID NO: 19, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 4, the VLCDR2 amino acid sequence of SEQ ID NO: 5, and the VLCDR3 amino acid sequence of SEQ ID NO: 6.

[0011] In some embodiments, the antibody or antibody fragment comprises a heavy chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 8. In some embodiments, the antibody or antibody fragment comprises a heavy chain variable sequence having at least 95% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 95% identity to SEQ ID NO: 8. In some embodiments, the antibody or antibody fragment comprises a heavy chain variable sequence having the sequence set forth in SEQ ID NO: 7 and a light chain variable sequence having the sequence set forth in SEQ ID NO: 8.

[0012] In some embodiments, the antibody or antibody fragment is humanized. In some embodiments, the antibody fragment is a monovalent scFv (single chain fragment variable) antibody, a bivalent scFv', a Fab fragment, a F(ab')2 fragment, a F(ab')3 fragment, an Fv fragment, or a single-chain antibody. In some embodiments, the antibody is a chimeric antibody, a bispecific antibody, or a BiTE. In some embodiments, the antibody is an IgG antibody or a recombinant IgG antibody or antibody fragment.

[0013] In one embodiment, provided herein is a monoclonal antibody or antibody fragment that competes for binding to the same epitope as a monoclonal antibody or antibody fragment according to any one of the present embodiments.

[0014] In one embodiment, provided herein is a monoclonal antibody or antibody fragment that binds to an epitope on B7-H3 recognized by an antibody of any one of the present embodiments.

[0015] In some embodiments, the antibody or antibody fragment is conjugated or fused to an imaging agent, a cytotoxic agent, a metal, or a radioactive moiety. In some embodiments, the imaging agent is a fluorophore. In some embodiments, the radioactive moiety is Zr-89, Cu-64, F-18, Y-90, Lu-177, At-211, Ac-225, or Pb-212.

[0016] In some embodiments, the antibody or antibody fragment is an immunoconjugate. In some embodiments, the antibody or antibody fragment is conjugated to flagellin or a flagellin derivative.

[0017] In some embodiments, the antibody or antibody fragment is an antibody-drug conjugate.

[0018] In one embodiment, provided herein is an isolated nucleic acid encoding the antibody heavy and / or light chain variable region of any of the antibody molecules of the present embodiments. In some embodiments, the nucleic acid comprises a nucleotide sequence at least 85% identical to SEQ ID NO: 9. In some embodiments, the nucleic acid comprises a nucleotide sequence at least 85% identical to SEQ ID NO: 10.

[0019] In one embodiment, provided herein is an expression vector comprising the nucleic acid of any one of the embodiments.

[0020] In one embodiment, provided herein is a hybridoma or engineered cell comprising nucleic acid encoding the antibody or antibody fragment of any one of the present embodiments.

[0021] In one embodiment, provided herein is a method of making a monoclonal antibody or antibody fragment of any one of the present embodiments, the method comprising culturing a hybridoma or engineered cell of the present embodiments under conditions that allow expression of the antibody, and optionally isolating the antibody from the culture.

[0022] In one embodiment, provided herein is a pharmaceutical formulation comprising one or more antibodies or antibody fragments of any one of the present embodiments.

[0023] In one embodiment, provided herein is a method of treating a patient with cancer, the method comprising administering an effective amount of any one of the antibodies or antibody fragments of the present embodiments. In some embodiments, the cancer is determined to express elevated levels of B7-H3 compared to healthy tissue. In some embodiments, the cancer is renal cancer, pancreatic cancer, colorectal cancer, non-small cell lung cancer, ovarian cancer, bladder cancer, melanoma, prostate cancer, breast cancer, glioma, lymphoma, or neuroectodermal cancer. In some embodiments, the method further comprises administering at least a second anticancer therapy. In certain embodiments, the second anticancer therapy is chemotherapy, targeted anticancer therapy, immunotherapy, radiation therapy, radioimmunotherapy, phototherapy, gene therapy, surgery, hormone therapy, epigenetic modulation, antiangiogenic therapy, or cytokine therapy. In some embodiments, the patient has previously failed to respond to immune checkpoint inhibitors. In some embodiments, the patient has relapsed.

[0024] In one embodiment, provided herein is a chimeric antigen receptor (CAR) protein comprising an antigen-binding domain comprising a heavy chain variable region (VH) comprising the VHCDR1, VHCDR2, and VHCDR3 amino acid sequences from the MIL33B antibody, and a light chain variable region (VL) comprising the VLCDR1, VLCDR2, and VLCDR3 amino acid sequences from the MIL33B antibody.

[0025] In some embodiments, the antigen-binding domain comprises a heavy chain variable region (VH) comprising the VHCDR1, VHCDR2, and VHCDR3 amino acid sequences derived from SEQ ID NO: 7, and a light chain variable region (VL) comprising the VLCDR1, VLCDR2, and VLCDR3 amino acid sequences derived from SEQ ID NO: 8.

[0026] In some embodiments, the antigen-binding domain comprises heavy and light chain CDR sequences as follows: a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 1, the VHCDR2 amino acid sequence of SEQ ID NO: 2, and the VHCDR3 amino acid sequence of SEQ ID NO: 3, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 4, the VLCDR2 amino acid sequence of SEQ ID NO: 5, and the VLCDR3 amino acid sequence of SEQ ID NO: 6.

[0027] In some embodiments, the antigen-binding domain comprises heavy and light chain CDR sequences as follows: a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 11, the VHCDR2 amino acid sequence of SEQ ID NO: 12, and the VHCDR3 amino acid sequence of SEQ ID NO: 13, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 14, the VLCDR2 amino acid sequence of SEQ ID NO: 15, and the VLCDR3 amino acid sequence of SEQ ID NO: 16.

[0028] In some embodiments, the antigen-binding domain comprises heavy and light chain CDR sequences as follows: a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 17, the VHCDR2 amino acid sequence of SEQ ID NO: 18, and the VHCDR3 amino acid sequence of SEQ ID NO: 19, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 20, the VLCDR2 amino acid sequence of SEQ ID NO: 21, and the VLCDR3 amino acid sequence of SEQ ID NO: 6.

[0029] In some embodiments, the antigen-binding domain comprises heavy and light chain CDR sequences as follows: a heavy chain variable region (VH) comprising the VHCDR1 amino acid sequence of SEQ ID NO: 17, the VHCDR2 amino acid sequence of SEQ ID NO: 18, and the VHCDR3 amino acid sequence of SEQ ID NO: 19, and a light chain variable region (VL) comprising the VLCDR1 amino acid sequence of SEQ ID NO: 4, the VLCDR2 amino acid sequence of SEQ ID NO: 5, and the VLCDR3 amino acid sequence of SEQ ID NO: 6.

[0030] In some embodiments, the antigen-binding domain is capable of binding to B7-H3. In some embodiments, the antigen-binding domain is a humanized antigen-binding domain.

[0031] In some embodiments, the antigen binding domain comprises a heavy chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 8. In some embodiments, the antigen binding domain comprises a heavy chain variable sequence having at least 95% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 95% identity to SEQ ID NO: 8. In some embodiments, the antigen binding domain comprises a heavy chain variable sequence having a sequence according to SEQ ID NO: 7 and a light chain variable sequence having a sequence according to SEQ ID NO: 8.

[0032] In some embodiments, the CAR protein further comprises a hinge domain, a transmembrane domain, and an intracellular signaling domain. In some embodiments, the hinge domain is a CD8a hinge domain or an IgG4 hinge domain. In some embodiments, the transmembrane domain is a CD8a transmembrane domain or a CD28 transmembrane domain. In some embodiments, the intracellular signaling domain comprises a CD3z intracellular signaling domain.

[0033] In one embodiment, the present disclosure provides a nucleic acid molecule encoding any one of the CARs of this embodiment.In some embodiments, the sequence encoding the CAR is operably linked to an expression control sequence.In some embodiments, the nucleic acid is further defined as an expression vector.

[0034] In one embodiment, provided herein is an engineered cell comprising a nucleic acid molecule encoding any one of the chimeric antigen receptors (CARs) of the present embodiments. In some embodiments, the cell is a T cell. In some embodiments, the cell is a NK cell. In some embodiments, the nucleic acid is integrated into the genome of the cell. In some embodiments, the cell is a human cell.

[0035] In one embodiment, provided herein is a pharmaceutical composition comprising a cell population according to any one of the present embodiments in a pharmaceutically acceptable carrier.

[0036] In one embodiment, provided herein is a method of treating cancer in a human patient in need thereof, comprising administering to the patient an anti-tumor effective amount of a cell therapy comprising one or more cells according to any one of the present embodiments. In some embodiments, the cells are allogeneic cells. In some embodiments, the cells are autologous cells. In some embodiments, the cells are HLA-matched to the subject. In some embodiments, the cancer is determined to express elevated levels of B7-H3 compared to healthy tissue. In some embodiments, the cancer is renal cancer, pancreatic cancer, colorectal cancer, non-small cell lung cancer, ovarian cancer, bladder cancer, melanoma, prostate cancer, breast cancer, glioma, lymphoma, or neuroectodermal cancer.

[0037] In some embodiments, the method further comprises administering at least a second anticancer therapy. In some embodiments, the second anticancer therapy is chemotherapy, molecular targeted therapy, immunotherapy, radiation therapy, radioimmunotherapy, phototherapy, gene therapy, surgery, hormone therapy, epigenetic modulation, antiangiogenic therapy, or cytokine therapy. In some embodiments, the patient has previously failed to respond to immune checkpoint inhibitors. In some embodiments, the patient has relapsed.

[0038] In one embodiment, provided herein is a method of diagnosing a patient as having a B7-H3-expressing cancer, the method comprising contacting cancer tissue obtained from the patient with the antibody or antibody fragment of any one of the present embodiments and detecting binding of the antibody or antibody fragment to the tissue, wherein if the antibody or antibody fragment binds to the tissue, the patient is diagnosed as having a B7-H3-expressing cancer. In some embodiments, the detecting comprises performing ELISA, immunoblotting, immunohistochemistry, multispectral fluorescence cytometry imaging, FACS, CyTOF mass cytometry (CyTOF), imaging mass cytometry (IMC), optical imaging, PET imaging, SPECT imaging, or MRI. In some embodiments, the method further comprises administering to a patient diagnosed with a B7-H3-expressing cancer an effective amount of an antibody or antibody fragment according to any one of the present embodiments, or an effective amount of a cell therapy comprising one or more cells.

[0039] In one embodiment, provided herein is a method of selecting a patient having cancer for treatment with an anti-B7-H3 antibody, the method comprising: (a) determining whether the cancer expresses B7-H3; and (b) selecting the patient for treatment if B7-H3 is expressed by the cancer. In some embodiments, step (a) comprises (i) obtaining or having obtained a biological sample from the patient; and (ii) performing or having performed an assay on the biological sample to determine whether B7-H3 is expressed in the cancer. In some embodiments, the method further comprises administering to the selected patient an effective amount of an antibody or antibody fragment according to any one of the present embodiments, or an effective amount of a cell therapy comprising one or more cells.

[0040] In some embodiments, whether B7-H3 is expressed in cancer is determined by detecting B7-H3 protein in sample.In some embodiments, protein is detected by mass cytometry, imaging mass cytometry, Western blot, FACS, immunohistochemistry, ELISA, RIA, optical imaging, PET imaging, SPECT imaging or MRI.In some embodiments, protein is detected by contacting cancer sample with any one of the antibodies of the present embodiment.

[0041] In one embodiment, provided herein is a method for detecting the presence of B7-H3 on the surface of a cell, in a tissue, in an organ, or in a biological sample, the method comprising: (a) contacting the cell, tissue, organ, or biological sample with an antibody of any one of the present embodiments; and (b) detecting the presence of the antibody bound to the cell, tissue, organ, or sample. In some embodiments, the contacting and detecting are in vitro. In some embodiments, the contacting and detecting are in vivo and the detecting are in vitro. In certain embodiments, the imaging agent is a fluorophore or chromophore. In some embodiments, the contacting and detecting are in vivo. In certain embodiments, the imaging agent is a radionuclide. In certain embodiments, the detection is by PET, SPECT, MRI, or hyperpolarized MRI. In certain embodiments, the detection is by hyperpolarized MRI and the detectable label is a Si-29 nanoparticle.

[0042] In one embodiment, provided herein is a method of performing fluorescence-guided surgery, the method comprising: (a) administering to a patient a composition comprising the antibody conjugate of the present embodiment under conditions and for a time sufficient to allow the antibody to accumulate at a given surgical site; (b) illuminating the surgical site with excitation light to cause emission of light from the fluorescent moiety; and (c) performing surgical resection of the region that fluoresces upon excitation with the excitation light.

[0043] In one embodiment, provided herein is an antibody molecule or pharmaceutical composition of any one of the embodiments for use in treating cancer in a subject.

[0044] In one embodiment, provided herein is the use of an antibody molecule or pharmaceutical composition of any one of the embodiments in the manufacture of a medicament for treating cancer in a subject.

[0045] As used herein, "essentially free" with respect to a particular component means that none of the particular components are intentionally formulated into the composition and / or are present only as contaminants or in trace amounts.The total amount of the particular component resulting from any unintentional contamination of the composition is therefore well below 0.05%, preferably below 0.01%.Most preferred is a composition in which the amount of the particular component cannot be detected using standard analytical methods.

[0046] As used herein, "a" or "an" may mean one or more. As used herein in the claims, when used in conjunction with the word "comprising," the words "a" or "an" may mean one or more than one.

[0047] Although the use of the term "or" in the claims is used to mean "and / or" unless expressly indicated to refer to alternatives only or the alternatives are not mutually exclusive, the present disclosure supports a definition that refers to alternatives only and "and / or." As used herein, "another" may mean at least a second or more.

[0048] Throughout this application, the term "about" is used to indicate that a value includes the inherent variation of error for the device, the method used to determine the value, the variation that exists between test subjects, or a value within 10% of the stated value.

[0049] [The present invention 1001] A monoclonal antibody or antibody fragment comprising a heavy chain variable region (VH) comprising the VHCDR1, VHCDR2, and VHCDR3 amino acid sequences from the MIL33B antibody, and a light chain variable region (VL) comprising the VLCDR1, VLCDR2, and VLCDR3 amino acid sequences from the MIL33B antibody. [The present invention 1002] A monoclonal antibody or antibody fragment of the present invention, comprising a heavy chain variable region (VH) comprising VHCDR1, VHCDR2, and VHCDR3 amino acid sequences derived from SEQ ID NO: 7, and a light chain variable region (VL) comprising VLCDR1, VLCDR2, and VLCDR3 amino acid sequences derived from SEQ ID NO: 8. [The present invention 1003] The monoclonal antibody or antibody fragment of the present invention 1001 or 1002, comprising a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 1, a VHCDR2 amino acid sequence comprising SEQ ID NO: 2, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 3, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 4, a VLCDR2 amino acid sequence comprising SEQ ID NO: 5, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6. [The present invention 1004] The monoclonal antibody or antibody fragment of the present invention 1001 or 1002, comprising a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 11, a VHCDR2 amino acid sequence comprising SEQ ID NO: 12, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 13, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 14, a VLCDR2 amino acid sequence comprising SEQ ID NO: 15, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 16. [The present invention 1005] The monoclonal antibody or antibody fragment of the present invention 1001 or 1002, comprising a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 17, a VHCDR2 amino acid sequence comprising SEQ ID NO: 18, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 19, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 20, a VLCDR2 amino acid sequence comprising SEQ ID NO: 21, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6. [The present invention 1006] The monoclonal antibody or antibody fragment of the present invention 1001 or 1002, comprising a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 17, a VHCDR2 amino acid sequence comprising SEQ ID NO: 18, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 19, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 4, a VLCDR2 amino acid sequence comprising SEQ ID NO: 5, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6. [The present invention 1007] A monoclonal antibody or antibody fragment of any of claims 1001 to 1006, comprising a heavy chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 8. [The present invention 1008] A monoclonal antibody or antibody fragment of any of claims 1001 to 1006, comprising a heavy chain variable sequence having at least 95% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 95% identity to SEQ ID NO: 8. [The present invention 1009] The monoclonal antibody or antibody fragment of any one of claims 1001 to 1006, comprising a heavy chain variable sequence having the sequence set forth in SEQ ID NO:7 and a light chain variable sequence having the sequence set forth in SEQ ID NO:8. [The present invention 1010] The monoclonal antibody or antibody fragment of any one of claims 1001 to 1009, wherein the antibody is capable of binding to B7-H3. [The present invention 1011] The monoclonal antibody or antibody fragment of any one of 1001 to 1010 of the present invention, which is a humanized antibody. [The present invention 1012] The antibody fragment may be a monovalent scFv (single chain fragment variable) antibody, a bivalent scFv, a Fab fragment, a F(ab') 2 Fragment, F(ab') 3 The monoclonal antibody or antibody fragment of any one of claims 1001 to 1011, which is a fragment, Fv fragment, or single-chain antibody. [The present invention 1013] The monoclonal antibody or antibody fragment of any one of claims 1001 to 1012, wherein the antibody is a chimeric antibody, a bispecific antibody, or a BiTE. [The present invention 1014] The monoclonal antibody or antibody fragment of any of claims 1001 to 1013, wherein the antibody is an IgG antibody or a recombinant IgG antibody or antibody fragment. [The present invention 1015] A monoclonal antibody or antibody fragment that competes with the monoclonal antibody or antibody fragment of any one of the present inventions 1001 to 1014 for binding to the same epitope. [The present invention 1016] A monoclonal antibody or antibody fragment that binds to an epitope on B7-H3 recognized by any of the antibodies of the present inventions 1001 to 1014. [The present invention 1017] 1016. The monoclonal antibody or antibody fragment of any of claims 1001 to 1016, wherein said antibody is conjugated or fused to an imaging agent, a cytotoxic agent, a metal, or a radioactive moiety. [The present invention 1018] 1017. The monoclonal antibody or antibody fragment of the invention, wherein said imaging agent is a fluorophore. [The present invention 1019] 1017. The monoclonal antibody or antibody fragment of the present invention, wherein the radioactive moiety is Zr-89, Cu-64, F-18, Y-90, Lu-177, At-211, Ac-225, or Pb-212. [The present invention 1020] The monoclonal antibody or antibody fragment of any one of claims 1001 to 1016, wherein the antibody is an immunoconjugate. [The present invention 1021] The monoclonal antibody or antibody fragment of the present invention 1020, wherein said antibody is conjugated to flagellin or a flagellin derivative. [The present invention 1022] The monoclonal antibody or antibody fragment of any one of claims 1001 to 1016, wherein the antibody is an antibody-drug conjugate. [The present invention 1023] An isolated nucleic acid encoding an antibody heavy chain and / or light chain variable region of the antibody molecule of any one of 1001 to 1016 of the present invention. [The present invention 1024] 1023. An isolated nucleic acid of the present invention comprising a nucleotide sequence that is at least 85% identical to SEQ ID NO:9. [The present invention 1025] 1023. An isolated nucleic acid of the present invention comprising a nucleotide sequence that is at least 85% identical to SEQ ID NO:10. [The present invention 1026] An expression vector comprising any one of the nucleic acids of the present inventions 1023 to 1025. [The present invention 1027] A hybridoma or engineered cell comprising a nucleic acid encoding the antibody or antibody fragment of any of claims 1001 to 1016. [The present invention 1028] A hybridoma or engineered cell comprising any one of the nucleic acids of the present inventions 1023 to 1025. [The present invention 1029] A method for producing a monoclonal antibody or antibody fragment of any of claims 1001 to 1018, comprising culturing a hybridoma or engineered cell of claim 1027 or 1028 under conditions that allow expression of said antibody, and optionally isolating said antibody from the culture. [The present invention 1030] A pharmaceutical formulation comprising one or more antibodies or antibody fragments according to any one of claims 1001 to 1022. [The present invention 1031] A method for treating a patient with cancer, comprising administering an effective amount of the antibody or antibody fragment of any of claims 1001 to 1022 of the present invention. [The present invention 1032] The method of claim 1031, wherein said cancer is determined to express elevated levels of B7-H3 compared to healthy tissue. [The present invention 1033] 1031. The method of claim 1031, wherein said cancer is renal cancer, pancreatic cancer, colorectal cancer, non-small cell lung cancer, ovarian cancer, bladder cancer, melanoma, prostate cancer, breast cancer, glioma, lymphoma, or neuroectodermal cancer. [The present invention 1034] The method of claim 1031, further comprising administering at least a second anti-cancer therapy. [This invention 1035] 1035. The method of claim 1034, wherein said second anticancer therapy is chemotherapy, targeted anticancer therapy, immunotherapy, radiation therapy, radioimmunotherapy, phototherapy, gene therapy, surgery, hormone therapy, epigenetic modulation, antiangiogenic therapy, or cytokine therapy. [The present invention 1036] The method of claim 1031, wherein said patient has previously failed to respond to an immune checkpoint inhibitor. [This invention 1037] The method of claim 1031, wherein the patient is experiencing a relapse. [The present invention 1038] A chimeric antigen receptor (CAR) protein comprising an antigen-binding domain comprising a heavy chain variable region (VH) comprising the VHCDR1, VHCDR2, and VHCDR3 amino acid sequences from the MIL33B antibody, and a light chain variable region (VL) comprising the VLCDR1, VLCDR2, and VLCDR3 amino acid sequences from the MIL33B antibody. [This invention 1039] A CAR of the present invention 1038, wherein the antigen-binding domain comprises a heavy chain variable region (VH) comprising VHCDR1, VHCDR2, and VHCDR3 amino acid sequences derived from SEQ ID NO: 7, and a light chain variable region (VL) comprising VLCDR1, VLCDR2, and VLCDR3 amino acid sequences derived from SEQ ID NO: 8. [The present invention 1040] the antigen-binding domain comprising: a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 1, a VHCDR2 amino acid sequence comprising SEQ ID NO: 2, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 3, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 4, a VLCDR2 amino acid sequence comprising SEQ ID NO: 5, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6; The CAR of the present invention 1038 or 1039, comprising heavy and light chain CDR sequences as follows: [This invention 1041] the antigen-binding domain comprising: a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 11, a VHCDR2 amino acid sequence comprising SEQ ID NO: 12, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 13, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 14, a VLCDR2 amino acid sequence comprising SEQ ID NO: 15, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 16; The CAR of the present invention 1038 or 1039, comprising heavy and light chain CDR sequences as follows: [The present invention 1042] the antigen-binding domain comprising: a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 17, a VHCDR2 amino acid sequence comprising SEQ ID NO: 18, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 19, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 20, a VLCDR2 amino acid sequence comprising SEQ ID NO: 21, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6; The CAR of the present invention 1038 or 1039, comprising heavy and light chain CDR sequences as follows: [This invention 1043] the antigen-binding domain comprising: a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 17, a VHCDR2 amino acid sequence comprising SEQ ID NO: 18, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 19, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 4, a VLCDR2 amino acid sequence comprising SEQ ID NO: 5, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6; The CAR of the present invention 1038 or 1039, comprising heavy and light chain CDR sequences as follows: [This invention 1044] A CAR of any of claims 1038 to 1043, wherein the antigen-binding domain comprises a heavy chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 70%, 80%, or 90% identity to SEQ ID NO: 8. [This invention 1045] A CAR of any of claims 1038 to 1043, wherein the antigen-binding domain comprises a heavy chain variable sequence having at least 95% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 95% identity to SEQ ID NO: 8. [The present invention 1046] The CAR of any of claims 1038 to 1043, wherein the antigen-binding domain comprises a heavy chain variable sequence having the sequence set forth in SEQ ID NO: 7 and a light chain variable sequence having the sequence set forth in SEQ ID NO: 8. [This invention 1047] The CAR of any one of 1038 to 1046, wherein the antigen-binding domain is capable of binding to B7-H3. [This invention 1048] The CAR of any of claims 1038 to 1047, wherein the antigen-binding domain is a humanized antigen-binding domain. [This invention 1049] The CAR of any one of 1038 to 1048, further comprising a hinge domain, a transmembrane domain, and an intracellular signaling domain. [The present invention 1050] The CAR of the present invention 1049, wherein the hinge domain is a CD8a hinge domain or an IgG4 hinge domain. [This invention 1051] The CAR of the present invention 1049, wherein the transmembrane domain is a CD8a transmembrane domain or a CD28 transmembrane domain. [This invention 1052] The CAR of the present invention 1049, wherein the intracellular signaling domain comprises a CD3z intracellular signaling domain. [This invention 1053] A nucleic acid molecule encoding any one of CARs 1038 to 1052 of the present invention. [This invention 1054] 1053. The nucleic acid molecule of claim 1053, wherein the sequence encoding the CAR is operably linked to an expression control sequence. [This invention 1055] The nucleic acid molecule of the present invention 1053 further defined as an expression vector. [The present invention 1056] An engineered cell comprising a nucleic acid molecule encoding the chimeric antigen receptor (CAR) of any of claims 1038 to 1052. [This invention 1057] The cell of the present invention 1056, which is a T cell. [This invention 1058] The cell of the present invention 1056, which is a NK cell. [This invention 1059] The cell of claim 1056, wherein the nucleic acid is integrated into the genome of the cell. [The present invention 1060] The cell of the present invention 1056, which is a human cell. [The present invention 1061] A pharmaceutical composition comprising a population of cells according to any one of the present inventions 1056 to 1061 in a pharmaceutically acceptable carrier. [The present invention 1062] A method of treating cancer in a human patient in need thereof, comprising administering to said patient an anti-tumor effective amount of a cell therapy comprising one or more cells of any of claims 1056 to 1061 of the present invention. [The present invention 1063] 1063. The method of claim 1062, wherein said cells are allogeneic cells. [The present invention 1064] 1063. The method of claim 1062, wherein the cells are autologous cells. [This invention 1065] 1063. The method of claim 1062, wherein said cells are HLA-matched to said subject. [The present invention 1066] The method of claim 1062, wherein said cancer is determined to express elevated levels of B7-H3 compared to healthy tissue. [This invention 1067] 1063. The method of claim 1062, wherein said cancer is renal cancer, pancreatic cancer, colorectal cancer, non-small cell lung cancer, ovarian cancer, bladder cancer, melanoma, prostate cancer, breast cancer, glioma, lymphoma, or neuroectodermal cancer. [The present invention 1068] The method of claim 1062, further comprising administering at least a second anti-cancer therapy. [This invention 1069] 1068. The method of claim 1068, wherein said second anticancer therapy is chemotherapy, molecular targeted therapy, immunotherapy, radiation therapy, radioimmunotherapy, phototherapy, gene therapy, surgery, hormone therapy, epigenetic modulation, antiangiogenic therapy, or cytokine therapy. [The present invention 1070] The method of claim 1062, wherein said patient has previously failed to respond to an immune checkpoint inhibitor. [This invention 1071] The method of claim 1062, wherein the patient is experiencing a relapse. [This invention 1072] A method for diagnosing a patient as having a cancer that expresses B7-H3, the method comprising the steps of contacting cancer tissue obtained from the patient with any one of the antibodies or antibody fragments of present inventions 1001 to 1022, and detecting binding of the antibody or antibody fragment to the tissue, wherein if the antibody or antibody fragment binds to the tissue, the patient is diagnosed as having a cancer that expresses B7-H3. [This invention 1073] The method of claim 1072, wherein the detecting step comprises performing ELISA, immunoblotting, immunohistochemistry, multispectral fluorescence cytometry imaging, FACS, mass cytometry (CyTOF), imaging mass cytometry (IMC), optical imaging, PET imaging, SPECT imaging, or MRI. [This invention 1074] The method of claim 1072, further comprising administering to said patient diagnosed with a cancer that expresses B7-H3 an effective amount of an antibody or antibody fragment of any of claims 1001 to 1025, or an effective amount of a cell therapy comprising one or more cells of any of claims 1060 to 1065. [This invention 1075] 1. A method for selecting a patient having cancer for treatment with an anti-B7-H3 antibody, comprising: (a) determining whether the cancer expresses B7-H3; and (b) selecting the patient for treatment if B7-H3 is expressed by the cancer. [This invention 1076] The method of claim 1075, wherein step (a) comprises (i) obtaining or having obtained a biological sample from the patient, and (ii) performing or having performed an assay on the biological sample to determine whether B7-H3 is expressed in the cancer. [This invention 1077] The method of claim 1075 or 1076, further comprising administering to the selected patient an effective amount of an antibody or antibody fragment of any of claims 1001 to 1022, or an effective amount of a cell therapy comprising one or more cells of any of claims 1060 to 1065. [This invention 1078] 1077. The method of any one of claims 1075 to 1076, wherein whether B7-H3 is expressed in said cancer is determined by detecting B7-H3 protein in said sample. [This invention 1079] 1078. The method of claim 1078, wherein said protein is detected by mass cytometry, imaging mass cytometry, Western blot, FACS, immunohistochemistry, ELISA, RIA, optical imaging, PET imaging, SPECT imaging, or MRI. [The present invention 1080] The method of claim 1078, wherein said protein is detected by contacting said cancer sample with any of the antibodies of claims 1001 to 1022. [This invention 1081] A method for detecting the presence of B7-H3 on the surface of a cell, in a tissue, in an organ, or in a biological sample, comprising the steps of: (a) contacting the cell, tissue, organ, or biological sample with any of the antibodies of the present inventions 1001 to 1022; and (b) detecting the presence of the antibody bound to the cell, tissue, organ, or sample. [This invention 1082] 1081. The method of claim 1081, wherein said contacting and detecting steps are in vitro. [This invention 1083] 1081. The method of claim 1081, wherein said contacting step is in vivo and said detecting step is in vitro. [This invention 1084] 1084. The method of claim 1082 or 1083, wherein said imaging agent is a fluorophore or chromophore. [This invention 1085] 1081. The method of claim 1081, wherein said contacting and detecting steps are in vivo. [This invention 1086] 1085. The method of claim 105, wherein said imaging agent is a radionuclide or a contrast agent. [This invention 1087] 1085. The method of claim 1085, wherein said detecting is by PET, SPECT, optical, MRI, or hyperpolarized MRI. [This invention 1088] 1087. The method of claim 1087, wherein said detecting is by hyperpolarized MRI and the detectable label is a Si-29 nanoparticle. [This invention 1089] A method for performing fluorescence-guided surgery, comprising: (a) administering to a patient a composition comprising an antibody of the present invention under conditions and for a time sufficient to cause the antibody to accumulate at a given surgical site; (b) illuminating the surgical site with excitation light to cause emission of light from a fluorescent moiety; and (c) performing surgical resection of an area that fluoresces when excited by the excitation light. [The present invention 1090] The antibody molecule of any of claims 1001 to 1022 or the pharmaceutical composition of claim 1030 for use in treating cancer in a subject. [This invention 1091] 10. Use of an antibody molecule of any of claims 1001 to 1022 or a pharmaceutical composition of claim 1030 in the manufacture of a medicament for treating cancer in a subject. Other objects, features, and advantages of the present invention will become apparent from the following detailed description. It should be understood, however, that the detailed description and specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, and that various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description. [Brief explanation of the drawings]

[0050] The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.

[0051] [Figure 1] ELISA for binding of MIL33B to human 4Ig-B7-H3 and mouse 2Ig-B7-H3. [Figure 2] Example of MIL33B binding to human 4Ig-B7-H3. The dissociation constant, Kd, ​​was determined using a Biolayer Interferometry (Octet) assay. MIL33B was captured on the surface of an optical sensor. The surface was then placed in a solution of analyte, and the phase transition indicating binding was measured over time. The probe was then transferred to a solution without analyte, and the time course of off-bound binding was measured. This cycle was repeated at multiple analyte concentrations, and Kd was calculated from a global curve fit of the concentration and time dependence of analyte binding to the antibody. [Figure 3] Western blot of human 4Ig-B7-H3 and mouse 2Ig-B7-H3 expression in various cell lines. [Figure 4A]Figures 4A-C. Binding of Alexa594-labeled MIL33B and Alexa594-labeled isotype control IgG2a to cells expressing 4Ig-B7-H3 and / or 2Ig-B7-H3. Figure 4A shows high signal from human HeLa and HCT116 cells expressing native 4Ig-B7-H3. Note the low background fluorescence from cellular autofluorescence or labeled IgG2a. Furthermore, adding Alexa594-labeled MIL33B in the presence of a molar excess of unlabeled MIL33B reduces cellular fluorescence to background, demonstrating specificity. Figure 4B shows murine 4T1 cells expressing moderate native 2Ig-B7-H3 and engineered to express human 4Ig-B7-H3 or an empty vector control. Figure 4C shows murine Pan02 cells expressing 2Ig-B7-H3. [Figure 4B] See legend to Figure 4A. [Figure 4C] See legend to Figure 4A. [Figure 5] Conjugation of MIL33B with flagellin as confirmed by Western blot and its affinity analysis for binding to human 4Ig-B7-H3. [Figure 6]Figures 6A-D. Induction of NF-κB by flagellin-conjugated MIL33B. Figure 6A shows the κB-RE5-IκBα-Fluc reporter. Figure 6B shows the initial loss of light production from the TNF-α-induced (time = 0) loss of the IκBα-Fluc reporter, followed by an increase in light production from the κB response element (RE5)-induced resynthesis of IκBα-Fluc. MIL33B alone does not activate NF-κB signaling. Figure 6C shows the initial loss of light production followed by an increase in light production from the κB response element (RE5) that drives the resynthesis of IκBα-Fluc after treatment with flagellin and flagellin-conjugated MIL33B. Figure 6D shows the levels of IκBα-Fluc-mediated photon flux induced by flagellin-conjugated MIL33B and various concentrations of flagellin alone 4 hours after stimulation. There is signal equivalence between 1.8 nM flagellin and 18.2 nM MIL33B-flagellin conjugate. [Figure 7] In vivo detection of 4T1 murine breast tumors and B16F10 murine melanoma tumors expressing human 4Ig-B7-H3 or vector control by PET imaging using MIL33B conjugated to DFO and radiolabeled with 89Zr compared with isotype control IgG2a conjugated to DFO and radiolabeled with 89Zr. Coronal PET images as maximum intensity projections (MIPs) (left panel) and volumetric analysis (%ID / cc) at 24 and 72 hours after injection of radiolabeled MIL33B or isotype control antibody (center and right panels) are shown. In the center and right panels, in each pair of columns, the left column represents MIL33B, and the right column represents IgG2a. [Figure 8] Survival curves (top) and tumor growth curves (bottom) of mice bearing murine B16F10 tumors expressing 4Ig-B7-H3 treated with MIL33B monotherapy or untreated control (PBS vehicle). DETAILED DESCRIPTION OF THE INVENTION

[0052] Detailed Description B7-H3 is a co-inhibitory ligand expressed on the surface of many tumor cells as well as in the tumor microvasculature (Suh et al., 2003; Zang et al., 2007; Wang et al., 2012). It is thought to actively inhibit the effector function of cytotoxic T lymphocytes (CTLs) or induce the generation of regulatory T cells, all of which downregulate immune responses (Pardoll, 2012). Although both CTLA-4 and B7-H3 are members of the broad CD28 / B7 family, CTLA-4 and B7-H3 have non-redundant functions, and studies conducted in animal models suggest that the two pathways play distinct roles in immune regulation (Zang et al., 2007; Wang et al., 2012).

[0053] B7-H3 protein is expressed in most tumor cell types and tumor-associated vasculature (Seaman et al., 2017). For example, B7-H3 is overexpressed in kidney, pancreatic, colorectal, non-small cell lung, ovarian, bladder, melanoma, and neuroectodermal cancers (Loo et al., 2012), as well as prostate cancer cells (Zang et al., 2007; Koenig, 2014), indicating the broad applicability of targeting B7-H3 for therapy and imaging. For example, in prostatectomy specimens from 803 patients with localized disease, the majority (93%) of prostate tumors expressed B7-H3 (Zang et al., 2007). Furthermore, high levels of B7-H3 (and / or B7-H4, another co-inhibitory ligand) expression have been associated with a higher risk of clinical failure (metastasis) and death within 7 years, implicating these molecules as inhibitory immune checkpoints that act to suppress antitumor immune responses (Zang et al., 2007; Zang et al., 2003). In addition, kidney, melanoma, glioblastoma, thyroid, and pancreatic cancers show up to 99% positive staining for B7-H3 by IHC (Koenig, 2014). Most importantly, limited B7-H3 protein is present in normal human tissues (Koenig, 2014; Zang et al., 2003). B7-H3 is highly expressed on the surface of cancer cells and in the cancer vasculature, but not in normal tissues, providing an excellent target for anti-cancer immunotherapy, positron emission tomography (PET) and immuno-PET imaging, and bifunctional conjugate drug therapy.

[0054] Known anti-B7-H3 antibodies exhibit modest nanomolar affinity for either human or mouse B7-H3 alone [PMID: 22894780, PMID: 26487718, PMID: 28399408, PMID: 22615450]. These antibodies were developed in normal mice bearing murine 2Ig-B7-H3, which shows high homology and domain identity to human 4Ig-B7-H3 and human 2Ig-B7-H3. Therefore, thymus-induced tolerance to self-antigens may limit the repertoire of epitopes that can be discovered in normal mouse strains, such as the common C57B16 strain. Furthermore, B7-H3 shares significant homology with other paralogs of the B7 family, further limiting the accessibility of high-affinity epitopes that can be discovered in either normal or B7-H3 knockout mice.

[0055] While human-only affinity is clearly sufficient for clinical translation and the desired therapeutic use, the inability of human-only antibodies to recognize murine epitopes makes preclinical murine models difficult or impossible to perform. In the current era of combination therapy with immune checkpoint inhibitors, this is particularly problematic, necessitating the use of murine surrogate-active antibodies. On the other hand, antibodies that recognize only murine epitopes allow preclinical analysis in appropriate murine models but preclude translation to humans. An ideal monoclonal antibody would exhibit high affinity for an epitope shared by both the human and murine target, in this case B7-H3.

[0056] Thus, provided herein is the monoclonal antibody MIL33B, which has high dual-species affinity for human 4Ig-B7-H3 (picomolar) and mouse 2Ig-B7-H3 (nanomolar). MIL33B was developed from immunized New Zealand Black / White (NZBWF1 / J) mice, a strain with broken tolerance. The MIL33B antibody has higher affinity for human 4Ig-B7-H3 than any published or commercially available antibody. For moderately abundant targets in tumors and the human immune system, affinity is important for maximizing immune response processes such as antibody-dependent cellular cytotoxicity (ADCC), antibody-drug conjugate (ADC) therapy, radiation therapy, and imaging, and is always beneficial for functional inhibition of coupled biology, especially when the local concentration of competing ligands is high. Published K values ​​for commercially available antibodies, such as ch8H9 mAb (Ahmed et al., 2015) and Macrogenics (Loo et al., 2012), are all >5 nM (or 5,000 pM), representing a >25-fold affinity advantage over MIL33B. MIL33B antibodies can be used, at a minimum, in immunotherapy, combination immune checkpoint therapy, antibody conjugates, antibody-based radiotherapeutics, antibody-based PET / SPECT imaging agents, and antibody-based in vitro diagnostics.

[0057] I. Definition As used herein, "nucleic acid," "nucleic acid sequence," "oligonucleotide," "polynucleotide," or other grammatical equivalents refer to at least two nucleotides, either deoxyribonucleotides or ribonucleotides, or analogs thereof, covalently linked together. A polynucleotide is a polymer of any length, including, for example, 20, 50, 100, 200, 300, 500, 1000, 2000, 3000, 5000, 7000, 10,000, etc. Polynucleotides described herein generally contain phosphodiester bonds, but in some cases include nucleic acid analogs that may have at least one different linkage, such as phosphoramidate, phosphorothioate, phosphorodithioate, or O-methylphosphoramidite linkage, as well as peptide nucleic acid backbones and linkages. Mixtures of naturally occurring polynucleotides and analogs can be made; alternatively, mixtures of different polynucleotide analogs and mixtures of naturally occurring polynucleotides and analogs can be made. Genes or gene fragments, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, ribozymes, cDNA, cRNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers are non-limiting examples of polynucleotides. Polynucleotides may contain modified nucleotides, such as methylated nucleotides and nucleotide analogs. If present, modifications to the nucleotide structure may be imparted before or after assembly of the polymer. The sequence of nucleotides may be interrupted by non-nucleotide components. Polynucleotides may be further modified after polymerization, such as by conjugation with a labeling component. The term also includes both double-stranded and single-stranded molecules. Unless otherwise specified or required, the term polynucleotide encompasses both the double-stranded form and each of the two complementary single-stranded forms known or predicted to constitute the double-stranded form.Polynucleotides are composed of a specific sequence of four nucleotide bases: adenine (A), cytosine (C), guanine (G), thymine (T), and, when the polynucleotide is RNA, uracil (U). Thus, the term "polynucleotide sequence" is the alphabetical representation of a polynucleotide molecule. Unless otherwise indicated, a particular polynucleotide sequence also implicitly encompasses conservatively modified variants thereof (e.g., degenerate codon substitutions) and complementary sequences, as well as the explicitly indicated sequence. Specifically, degenerate codon substitutions can be achieved by generating sequences in which the third position of one or more selected (or all) codons is substituted with mixed-base and / or deoxyinosine residues.

[0058] As used herein, the terms "peptide," "polypeptide," and "protein" refer to a polymer of amino acid residues. These terms also apply to amino acid polymers in which one or more amino acid residues are artificial chemical mimetics of corresponding naturally occurring amino acids, as well as naturally occurring amino acid polymers, those containing modified residues, and non-natural amino acid polymers. In this example, the term "polypeptide" includes antibodies or fragments thereof.

[0059] As used herein, other terms used in the fields of recombinant nucleic acid technology, microbiology, immunology, antibody engineering, and molecular and cell biology will be commonly understood by those skilled in the art.

[0060] II. Antibodies and Antibody Modifications Provided herein are monoclonal antibodies having clone-paired complementarity-determining regions (CDRs) from the heavy and light chains as shown in Tables 1 to 3. Such antibodies can be produced using the methods described herein.

[0061] The monoclonal antibody of the present invention has several applications, including the preparation of diagnostic kits for detecting B7-H3 and the treatment of diseases associated with increased levels of B7-H3.In these contexts, such antibodies can be linked to diagnostic or therapeutic agents and used as capture or competitive agents in competitive assays, or used individually without additional agents bound to them.Antibodies can be mutated or modified, as further described below.Methods for preparing and characterizing antibodies are well known in the art (see, for example, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988, U.S. Patent No. 4,196,265).

[0062] An "antibody" is an immunoglobulin molecule capable of specifically binding to a target, such as a carbohydrate, polynucleotide, lipid, or polypeptide, via at least one antigen recognition site located in the variable region of the immunoglobulin molecule. As used herein, the term encompasses intact polyclonal or monoclonal antibodies, as well as fragments thereof (Fab, Fab', F(ab')2, Fv, Fd, Fd', single-chain antibodies (ScFv), diabodies, linear antibodies, etc.), mutants thereof, naturally occurring variants, fusion proteins comprising an antibody portion having an antigen recognition site of the required specificity, humanized antibodies, chimeric antibodies, and any other modified configuration of an immunoglobulin molecule containing an antigen recognition site of the required specificity.

[0063] An "isolated antibody" is one that has been separated and / or recovered from components of its natural environment. Contaminant components of its natural environment are substances that would interfere with diagnostic or therapeutic uses for the antibody, and may include enzymes, hormones, and other proteinaceous or non-proteinaceous solutes. In particular examples, antibodies are purified to (1) greater than 95% antibody by weight, most particularly greater than 99% by weight, as determined by the Lowry method, or (2) to homogeneity by SDS-PAGE under reducing or non-reducing conditions using Coomassie blue or silver staining. Isolated antibodies include antibodies in situ within recombinant cells, when at least one component of the antibody's natural environment will not be present. Ordinarily, however, isolated antibodies will be prepared by at least one purification step.

[0064] The basic four-chain antibody unit is a heterotetrameric glycoprotein composed of two identical light (L) chains and two identical heavy (H) chains. As used herein, the term "heavy chain" refers to a larger immunoglobulin subunit that is associated through its amino-terminal region with an immunoglobulin light chain. The heavy chain contains a variable region (V H ) and constant region (C H The constant region contains C H 1. Hinge, C H 2, and C H For IgE, IgM, and IgY, the heavy chain contains three domains: C H Heavy chains comprise four domains but lack a hinge domain. Those skilled in the art will understand that heavy chains are classified as gamma, mu, alpha, delta, or epsilon (γ, μ, α, δ, ε), with several subclasses within them (e.g., γ1-γ4, α1-α2). It is the nature of this chain that determines the "class" of an antibody, as IgG, IgM, IgA, IgD, or IgE, respectively. Immunoglobulin subclasses (isotypes), e.g., IgG1, IgG2, IgG3, IgG4, IgA1, etc., are well characterized and are known to confer functional specialization.

[0065] As used herein, the term "light chain" refers to the smaller immunoglobulin subunit associated with the amino-terminal region of a heavy chain. Like heavy chains, light chains contain a variable region (V L ) and constant region (C L The light chains contain their constant domains (C L Light chains are classified as either kappa or lambda (κ, λ) based on the amino acid sequence of their heavy chains. These pairs can associate with any pair of heavy chains to form immunoglobulin molecules. The term light chain also includes a light chain having a lambda variable region (V-lambda) linked to a kappa constant region (C-kappa) or a kappa variable region (V-kappa) linked to a lambda constant region (C-lambda).

[0066] For example, IgM antibodies consist of five basic heterotetrameric units together with an additional polypeptide called the J chain, and therefore contain 10 antigen-binding sites, whereas secretory IgA antibodies can polymerize to form multivalent assemblies containing two to five basic four-chain units together with the J chain. In the case of IgG, the four-chain unit is generally about 150,000 daltons. Each L chain is linked to an H chain by one covalent disulfide bond, and the two H chains are linked to each other by one or more disulfide bonds depending on the H chain isotype. Each H and L chain also has regularly spaced intrachain disulfide bridges. Each H chain contains a variable region (V) at its N-terminus. H ), followed by three constant domains for each of the alpha and gamma chains (C H ), and four Cs in mu and isotype H Each L chain has a variable domain (V L ), followed by a constant domain (C L ) V L is V H Align with C L is the first constant domain of the heavy chain (C H 1). Certain amino acid residues are thought to form an interface between the light-chain variable region and the heavy-chain variable region. V H and V LThe pairing of these two antibodies together forms a single antigen-binding site. For the structure and properties of different classes of antibodies, see, e.g., Basic and Clinical Immunology, 8th edition, Daniel P. Stites, Abba I. Terr and Tristram G. Parslow (eds.), Appleton & Lange, Norwalk, Conn., 1994, page 71 and Chapter 6.

[0067] The "variable region" of an antibody refers to the variable region of the antibody light chain or the variable region of the antibody heavy chain, either alone or in combination. The term "variable" refers to the fact that certain segments of the variable region differ significantly in sequence among antibodies. L ) and heavy chain (V H The variable regions of both heavy and light chains mediate antigen binding and define the specificity of a particular antibody for its particular antigen. However, variability is not uniformly distributed throughout the variable regions. Instead, variable regions consist of relatively invariant sections called framework regions (FRs) separated by shorter regions of extreme variability called complementarity-determining regions (CDRs) or hypervariable regions. Native heavy and light chain variable regions each contain four FRs that primarily adopt a beta-sheet structure, connected by three CDRs, and form loops that connect, and in some cases form part of, the beta-sheet structure. The CDRs complement the shape of the antigen and determine the affinity and specificity of the antibody for the antigen. V L and V H There are six CDRs in both the ribosomal and ribosomal amino acids. The CDRs in each chain are held together in close proximity by FRs and, with the CDRs from the other chain, contribute to the formation of the antigen-binding site of antibodies (see Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1991)).

[0068] As used herein, the term "hypervariable region" refers to the amino acid residues of an antibody that are responsible for antigen binding. Hypervariable regions generally consist of amino acid residues from the "complementarity determining regions" or "CDRs" (e.g., the V and V sequences when numbered according to the Kabat numbering system). L Around residues 24-34 (L1), 50-56 (L2), and 89-97 (L3) in V H These residues are located around approximately 31-35 (H1), 50-65 (H2), and 95-102 (H3) in the H1 sequence (Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1991)), and / or those residues from the "hypervariable loops" (e.g., V1 and V2 when numbered according to the Chothia numbering system). L Residues 24–34 (L1), 50–56 (L2), and 89–97 (L3) in V H 26-32 (H1), 52-56 (H2), and 95-101 (H3) in (Chothia and Lesk, J. Mol. Biol. 196:901-917 (1987)), and / or those residues from the "hypervariable loops" / CDRs (e.g., V when numbered according to the IMGT numbering system). L Residues 27–38 (L1), 56–65 (L2), and 105–120 (L3) in V H 27-38 (H1), 56-65 (H2), and 105-120 (H3) in the V-seq. antibody. Optionally, the antibody is numbered according to A. Ho, Honneger, A., and Plunkthun, A. J. Mol. Biol. 309:657-670 (2001). L 28, 36 (L1), 63, 74-75 (L2), and 123 (L3) in V subThe CDRs have symmetric insertions at one or more of the following positions in H: 28, 36 (H1), 63, 74-75 (H2), and 123 (H3). As used herein, CDRs may refer to CDRs defined by any of these numbering approaches, or by a combination of approaches, or by any other desired approach. In addition, novel definitions of highly conserved core, boundary, and hypervariable regions may be used.

[0069] A "constant region" of an antibody refers to the constant region of the antibody light chain or the constant region of the antibody heavy chain, either alone or in combination. L ) and heavy chain (C H 1. C H 2, or C H 3 or C for IgM and IgE H The constant region of 4) confers important biological properties such as secretion, transplacental mobility, Fc receptor binding, and complement fixation. By convention, the numbering of constant region domains increases as they become more distal from the antigen-binding site or amino-terminus of the antibody. The constant region is not directly involved in binding of the antibody to the antigen, but exhibits various effector functions, such as antibody participation in antibody-dependent cellular cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP), antibody-dependent neutrophil phagocytosis (ADNP), and antibody-dependent complement deposition (ADCD).

[0070] An antibody may be an antibody fragment. An "antibody fragment" comprises only a portion of an intact antibody, generally including the antigen-binding site of the intact antibody, and thus retains the ability to bind to antigen. Examples of antibody fragments encompassed by this definition include: (i) V L , C L , V H , and C H1 (ii) a Fab fragment having a C domain; H1 (iii) a Fab' fragment, which is a Fab fragment having one or more cysteine ​​residues at the C-terminus of the V domain; H and C H (iv) Fd fragment having one domain, H and C H 1 domain and CH (v) a Fd' fragment having one or more cysteine ​​residues at the C-terminus of one domain; (v) a V L and V H (vi) Fv fragment having V domains; H (vii) isolated CDR regions; (viii) a F(ab')2 fragment, which is a bivalent fragment comprising two Fab' fragments linked by a disulfide bridge at the hinge region; (ix) a single-chain antibody molecule (e.g., single-chain Fv, scFv); (x) a light chain variable domain (V) on the same polypeptide chain; L ) connected to the heavy chain variable domain (V H (xi) a "diabody" having two antigen-binding sites, comprising a pair of tandem Fd segments (V) that, together with complementary light chain polypeptides, form a pair of antigen-binding regions. H -C H 1-V H -C H 1) and "linear antibodies."

[0071] The antibody may be a chimeric antibody. A "chimeric antibody" refers to an antibody in which one portion of the amino acid sequence of each of the heavy and light chains is homologous to the corresponding sequence in an antibody derived from a particular species or belonging to a particular class, while the remaining segments of the chain are homologous to the corresponding sequence in another antibody. For example, a chimeric antibody may contain an antigen-binding sequence from a non-human donor grafted onto heterologous non-human, human, or humanized sequences (e.g., framework and / or constant domain sequences). Typically, in these chimeric antibodies, the variable regions of both the light and heavy chains mimic the variable regions of antibodies derived from one mammalian species, while the constant regions are homologous to antibody sequences from another species. For example, methods have been developed to replace the light and heavy chain constant domains of a monoclonal antibody with similar domains of human origin, leaving the variable regions of the foreign antibody intact. Alternatively, "fully human" monoclonal antibodies have been produced in mice transgenic with human immunoglobulin genes. Methods have also been developed to convert the variable domains of monoclonal antibodies into more human forms by recombinantly constructing antibody variable domains with both rodent (e.g., mouse) and human amino acid sequences. In "humanized" monoclonal antibodies, only the hypervariable CDRs are derived from mouse monoclonal antibodies, while the framework and constant regions are derived from human amino acid sequences (see U.S. Pat. Nos. 5,091,513 and 6,881,557, incorporated herein by reference). Replacing amino acid sequences in rodent-specific antibodies with amino acid sequences found in the corresponding positions of human antibodies is thought to reduce the likelihood of adverse immune reactions during therapeutic use. Hybridomas or other cells producing antibodies can also be subjected to genetic mutations or other changes, which may or may not alter the binding specificity of the antibodies produced by the hybridoma.

[0072] A. Monoclonal antibodies As used herein, the term "monoclonal antibody" refers to an antibody obtained from a population of substantially homogeneous antibodies, i.e., the individual antibodies comprising the population are identical except for possible naturally occurring mutations that may be present in minor amounts. Monoclonal antibodies are highly specific, being directed against a single antigenic site. Furthermore, in contrast to polyclonal antibody preparations, which include different antibodies directed against different determinants (epitopes), each monoclonal antibody is directed against a single determinant on the antigen. In addition to their specificity, monoclonal antibodies are advantageous in that they may be synthesized uncontaminated by other antibodies. The modifier "monoclonal" should not be construed as requiring production of the antibody by any particular method. For example, monoclonal antibodies useful in the present disclosure can be prepared by the hybridoma methodology first described by Kohler et al., Nature, 256:495 (1975), or can be produced using recombinant DNA methods in bacteria, eukaryotic animal, or plant cells after single-cell sorting of antigen-specific B cells, antigen-specific plasmablasts, or capture of linked heavy and light chains from single cells in bulk-sorted antigen-specific collections in response to infection or immunity (see, for example, U.S. Patent No. 4,816,567). Monoclonal antibodies can be isolated from phage antibody libraries using the techniques described, for example, in Clackson et al., Nature, 352:624-628 (1991) and Marks et al., J. Mol. Biol., 222:581-597 (1991).

[0073] Methods for producing various types of monoclonal antibodies, including humanized, chimeric, and fully human, are known in the art and are highly predictable. For example, the following U.S. patents and patent applications provide enabling descriptions of such methods: U.S. Patent Application Nos. 2004 / 0126828 and 2002 / 0172677, and U.S. Patent Application Nos. 3,817,837, 3,850,752, 3,939,350, 3,996,345, 4,196,265, 4,275,149, 4,277,437, 4,366,241, 4,469,797, 4,472,5 No. 09, No. 4,606,855, No. 4,703,003, No. 4,742,159, No. 4,767,720, No. 4,816,567, No. 4,867,973, No. 4,9 No. 38,948, No. 4,946,778, No. 5,021,236, No. 5,164,296, No. 5,196,066, No. 5,223,409, No. 5,403,484, No. No. 5,420,253, No. 5,565,332, No. 5,571,698, No. 5,627,052, No. 5,656,434, No. 5,770,376, No. 5,789,208 No. 5,821,337, No. 5,844,091, No. 5,858,657, No. 5,861,155, No. 5,871,907, No. 5,969,108, No. 6,054 ,297, 6,165,464, 6,365,157, 6,406,867, 6,709,659, 6,709,873, 6,753,407, 6,814,965, 6,849,259, 6,861,572, 6,875,434, and 6,891,024, each of which is incorporated herein by reference.

[0074] B. Single chain antibody Single-chain variable fragments (scFvs) are fusions of the variable regions of immunoglobulin heavy and light chains linked together with a short linker. This chimeric molecule retains the specificity of the original immunoglobulin despite the removal of the constant region and the introduction of a linker peptide. This modification usually leaves specificity unchanged. scFvs can be produced directly from subcloned heavy and light chains from hybridomas or B cells. Single-chain variable fragments lack the constant Fc region found in intact antibody molecules and therefore lack the consensus binding sites (e.g., protein A / G) used to purify antibodies. These fragments can often be purified / immobilized using protein L because protein L interacts with the variable region of the kappa light chain.

[0075] Flexible linkers are generally composed of helix- and turn-promoting amino acid residues such as alanine, serine, and glycine. However, other residues can function as well. For example, a linker can be V H It may have a proline residue two residues after the C-terminus, as well as multiple arginines and prolines at other positions.

[0076] Single-chain antibodies can also be produced by linking the light and heavy chains of the receptor using a non-peptide linker or chemical unit. Generally, the light and heavy chains are produced in different cells, purified, and then linked together in an appropriate manner (i.e., the N-terminus of the heavy chain is linked to the C-terminus of the light chain via a suitable chemical bridge).

[0077] Cross-linking reagent is used to form a molecular bridge that connects the functional groups of two different molecules, such as stabilizer and coagulant.However, it is contemplated that the same analogue dimer or multimer, or the heteromeric complex of different analogues can be produced.To link two different compounds stepwise, heterobifunctional cross-linking reagent can be used, which eliminates unnecessary homopolymer formation.

[0078] Exemplary heterobifunctional crosslinkers contain two reactive groups, one that reacts with primary amine groups (e.g., N-hydroxysuccinimide) and the other that reacts with thiol groups (e.g., pyridyl disulfide, maleimide, halogen, etc.). Through the primary amine reactive group, the crosslinker can react with a lysine residue of one protein (e.g., a selected antibody or fragment), and through the thiol reactive group, the crosslinker already attached to the first protein reacts with a cysteine ​​residue (free sulfhydryl group) of the other protein (e.g., a selected agent).

[0079] It is preferable to use a crosslinker that has reasonable stability in blood.Many types of disulfide bond-containing linkers are known that can be successfully used to conjugate targeting agents and therapeutic / prophylactic agents.Containing sterically hindered disulfide bonds can be proven to provide greater stability in vivo and prevent the release of targeting peptides before reaching the site of action.Therefore, these linkers are a group of linking agents.

[0080] For example, SMPT is a bifunctional crosslinker containing a disulfide bond that is "sterically hindered" by the adjacent benzene ring and methyl group. It is believed that the steric hindrance of the disulfide bond serves to protect the bond from attack by thiolate anions, such as glutathione, that may be present in tissues and blood, thereby helping to prevent detachment of the conjugate before the attached drug is delivered to the target site. Like many other known crosslinking reagents, the SMPT crosslinking reagent offers the ability to crosslink functional groups such as the SH residue of cysteine ​​or primary amines (e.g., the epsilon-amino group of lysine). Another possible type of crosslinker includes heterobifunctional photoreactive phenyl azides containing a cleavable disulfide bond, such as sulfosuccinimidyl-2-(p-azidosalicylamido)ethyl-1,3'-dithiopropionate. The N-hydroxy-succinimidyl group reacts with primary amino groups, and the phenyl azide (upon photolysis) reacts nonselectively with any amino acid residue.

[0081] In addition to inhibiting crosslinkers, non-inhibiting linkers can also be used in accordance with the present invention. Other useful crosslinkers that are not thought to contain or generate protected disulfides include SATA, SPDP, and 2-iminothiolane. The use of such crosslinkers is well understood in the art. Flexible linkers can also be used.

[0082] U.S. Patent No. 4,680,338 describes bifunctional linkers useful for preparing conjugates of ligands with amine-containing polymers and / or proteins, particularly useful for forming antibody conjugates with chelators, drugs, enzymes, detectable labels, etc. U.S. Patent Nos. 5,141,648 and 5,563,250 disclose cleavable conjugates containing labile bonds that are cleavable under various mild conditions. This linker is particularly useful when a drug of interest can be directly attached to the linker, with cleavage resulting in the release of the active drug. Specific uses include adding free amino or free sulfhydryl groups to proteins such as antibodies or drugs.

[0083] U.S. Patent No. 5,856,456 provides peptide linkers for use in connecting polypeptide components to create fusion proteins, such as single-chain antibodies. The linkers are up to about 50 amino acids in length and contain at least one charged amino acid (preferably arginine or lysine) followed by proline, and are characterized by higher stability and reduced aggregation. U.S. Patent No. 5,880,270 discloses aminooxy-containing linkers useful in various immunodiagnostic and separation techniques.

[0084] C. Bispecific and Multispecific Antibodies Antibodies can be bispecific or multispecific. A "bispecific antibody" is an antibody that has binding specificities for at least two different epitopes. Exemplary bispecific antibodies can bind to two different epitopes of a single antigen. Other such antibodies may combine a first antigen-binding site with a second antigen-binding site. Alternatively, an antigen-specific arm may be combined with an arm that binds to a triggering molecule on leukocytes, such as a T cell receptor molecule (e.g., CD3), or an IgG Fc receptor (FcγR), such as FcγRI (CD64), FcγRII (CD32), and FcγRIII (CD16), to focus and localize cellular defense mechanisms to infected cells. Bispecific antibodies can also be used to localize cytotoxic agents to infected cells. These antibodies have an antigen-binding arm and an arm that binds to a cytotoxic agent (e.g., saporin, anti-interferon α, vinca alkaloid, ricin A chain, methotrexate, or a radioisotope hapten). Bispecific antibodies can be prepared as full-length antibodies or antibody fragments (e.g., F(ab')2 bispecific antibodies). Taki et al. (2015) reported a bispecific anti-B7-H3 / anti-CD3 antibody.

[0085] Methods for producing bispecific antibodies are known in the art. Traditional production of full-length bispecific antibodies is based on the co-expression of two immunoglobulin heavy chain-light chain pairs, with the two chains having different specificities. Due to the unselected combination of immunoglobulin heavy and light chains, these hybridomas (quadromas) produce a potential mixture of 10 different antibody molecules, of which only one has the correct bispecific structure. Purification of the correct molecule is usually performed by affinity chromatography steps, which is quite cumbersome and results in low production yields.

[0086] According to another approach, antibody variable regions with the desired binding specificities (antibody-antigen combining sites) are fused to immunoglobulin constant domain sequences. Preferably, the fusion is with an Ig heavy chain constant domain, including hinge, C H2 , and C H3The first heavy-chain constant region (C) containing the site necessary for light-chain binding, present in at least one of the fusions, H1 ) is preferred. DNA encoding the immunoglobulin heavy chain fusions, and optionally, the immunoglobulin light chain, are inserted into separate expression vectors and co-transfected into suitable host cells. This provides greater flexibility in adjusting the mutual ratios of the three polypeptide fragments when an unequal ratio of the three polypeptide chains used in the construct provides the optimal yield of the desired bispecific antibody. However, it is possible to insert the coding sequences for two or all three polypeptide chains into a single expression vector when expression of at least two polypeptide chains in equal ratios results in high yields, or when the ratio has no significant effect on the yield of the desired chain combination.

[0087] Bispecific antibodies can be composed of a hybrid immunoglobulin heavy chain with a first binding specificity in one arm and a hybrid immunoglobulin heavy chain-light chain pair (providing a second binding specificity) in the other arm. This asymmetric structure facilitates separation of the desired bispecific compound from undesired immunoglobulin chain combinations, as the presence of an immunoglobulin light chain in only one half of the bispecific molecule provides a facile method of separation. This approach is disclosed in WO 94 / 04690. For further details on generating bispecific antibodies, see, for example, Suresh et al., Methods in Enzymology, 121:210 (1986).

[0088] According to another approach described in U.S. Patent No. 5,731,168, the interface between a pair of antibody molecules can be engineered to maximize the percentage of heterodimers which are recovered from recombinant cell culture. A preferred interface is C H3The antibody comprises at least a portion of the antibody domain. In this method, one or more small amino acid side chains from the interface of a first antibody molecule are replaced with larger side chains (e.g., tyrosine or tryptophan). Compensatory "cavities" of identical or similar size to the large side chains are created at the interface of a second antibody molecule by replacing the large amino acid side chains with smaller ones (e.g., alanine or threonine). This provides a mechanism for increasing the yield of heterodimers over other unwanted end-products, such as homodimers.

[0089] Bispecific antibodies include cross-linked or "heteroconjugate" antibodies. For example, one of the antibodies in the heteroconjugate can be bound to avidin, and the other to biotin. Such antibodies have been proposed, for example, to target immune system cells to unwanted cells (U.S. Pat. No. 4,676,980). Heteroconjugate antibodies can be made using any convenient cross-linking method. Suitable cross-linking agents are well known in the art and are disclosed in U.S. Pat. No. 4,676,980, along with several cross-linking techniques.

[0090] Techniques for generating bispecific antibodies from antibody fragments have also been described in the literature. For example, bispecific antibodies can be prepared using chemical linkage. Brennan et al., Science, 229:81 (1985) reported a procedure in which intact antibodies were proteolytically cleaved to generate F(ab')2 fragments. These fragments were reduced in the presence of the dithiol complexing agent sodium arsenite to stabilize vicinal dithiols and prevent intermolecular disulfide formation. The generated Fab' fragments were then converted to thionitrobenzoate (TNB) derivatives. One of the Fab'-TNB derivatives was then reconverted to the Fab'-thiol by reduction with mercaptoethylamine and mixed with an equimolar amount of the other Fab'-TNB derivative to form the bispecific antibody. The resulting bispecific antibody can be used as an agent for the selective immobilization of enzymes.

[0091] Techniques exist to facilitate the direct recovery of Fab'-SH fragments from Escherichia coli (E. coli), which can then be chemically coupled to form bispecific antibodies. Shalaby et al., J. Exp. Med., 175:217-225 (1992) reported the production of humanized bispecific antibody F(ab')2 molecules. Each Fab' fragment was separately secreted from E. coli and subjected to direct chemical coupling in vitro to form the bispecific antibody. The bispecific antibody thus formed was capable of binding to cells overexpressing the ErbB2 receptor and normal human T cells, as well as triggering the lytic activity of human cytotoxic lymphocytes against human breast tumor targets.

[0092] Various techniques for producing and isolating bispecific antibody fragments directly from recombinant cell culture have also been reported (Merchant et al., Nat. Biotechnol. 16, 677-681 (1998)). For example, bispecific antibodies have been produced using leucine zippers (Kostelny et al., J. Immunol., 148(5):1547-1553, 1992). The leucine zipper peptides from Fos and Jun proteins were linked to the Fab' portions of two different antibodies by gene fusion. Antibody homodimers were reduced at the hinge region to form monomers and then reoxidized to form antibody heterodimers. This method can also be used to produce antibody homodimers. "Diabodies," reported by Hollinger et al., Proc. Natl. Acad. Sci. USA, 90:6444-6448 (1993), have provided an alternative mechanism for generating bispecific antibody fragments. The fragments are separated by a linker that is too short to allow pairing between the two domains on the same chain. L V connected to H Therefore, one fragment of V H and V L The domain is a complementary V L and V HThe antibody fragments are then paired with single-chain Fv (sFv) dimers, thereby forming two antigen-binding sites. Another strategy for making bispecific antibody fragments by the use of single-chain Fv (sFv) dimers has also been reported. See Gruber et al., J. Immunol., 152:5368 (1994).

[0093] Bispecific or multispecific antibodies can be formed as DOCK-AND-LOCK™ (DNL™) complexes (see, e.g., U.S. Patent Nos. 7,521,056, 7,527,787, 7,534,866, 7,550,143, and 7,666,400). Generally, this technology utilizes the specific and high-affinity binding interaction between the dimerization and docking domain (DDD) sequence of the regulatory (R) subunit of cAMP-dependent protein kinase (PKA) and the anchor domain (AD) sequence from any of various AKAP proteins (Baillie et al., FEBS Letters. 2005; 579:3264; Wong and Scott, Nat. Rev. Mol. Cell Biol. 2004; 5:959). The DDD and AD peptides can be bound to any protein, peptide, or other molecule. Because DDD sequences spontaneously dimerize and bind to AD sequences, this technique allows the formation of complexes between any selected molecules that can bind to DDD or AD sequences.

[0094] Antibodies with more than two binding valencies are contemplated. For example, trispecific antibodies can be prepared (Tutt et al., J.Immunol.147:60,1991; Xu et al., Science,358(6359):85-90,2017). Antibodies can also contain sequences or moieties that allow receptor dimerization or multimerization. Such sequences include sequences derived from IgA that bind with J chain to allow multimer formation. Another multimerization domain is the Gal4 dimerization domain.

[0095] Multivalent antibodies may be internalized (and / or catabolized) more quickly than bivalent antibodies by cells expressing the antigen to which the antibody binds. The antibodies of the present disclosure can be multivalent antibodies (e.g., tetravalent antibodies) having three or more antigen-binding sites, and can be readily produced by recombinant expression of nucleic acids encoding the antibody polypeptide chains. Multivalent antibodies can comprise a dimerization domain and three or more antigen-binding sites. A preferred dimerization domain comprises (or consists of) an Fc region or hinge region. In this scenario, the antibody comprises an Fc region and three or more antigen-binding sites amino-terminal to the Fc region. Multivalent antibodies can comprise (or consist of) three to about eight, e.g., four, antigen-binding sites. Multivalent antibodies comprise at least one polypeptide chain (preferably two polypeptide chains), and the polypeptide chains comprise two or more variable regions. For example, the polypeptide chains can be VD1-(X1).sub.n-VD2-(X2). n -Fc, where VD1 is a first variable region and VD2 is a second variable region, Fc is one polypeptide chain of the Fc region, X1 and X2 represent amino acids or polypeptides, and n is 0 or 1. For example, the polypeptide chain may comprise a VH-CH1-flexible linker-VH-CH1-Fc region chain or a VH-CH1-VH-CH1-Fc region chain. The multivalent antibody herein may further comprise at least two (preferably four) light chain variable region polypeptides. The multivalent antibody herein may comprise, for example, about two to about eight light chain variable region polypeptides. The light chain variable region polypeptide contemplated herein comprises a light chain variable region and, optionally, a C L Further includes domains.

[0096] Charge modifications are particularly useful in the context of multispecific antibodies, where amino acid substitutions in Fab molecules result in reduced mispairing of light chains with non-matching heavy chains (Bence-Jones by-products), which can occur in the production of Fab-based bi / multispecific antigen-binding molecules with VH / VL exchange in one (or more in the case of molecules comprising more than two antigen-binding Fab molecules) of their binding arms (see also PCT Publication No. 2015 / 150447, especially the Examples therein, which is incorporated herein by reference in its entirety).

[0097] D.BiTE Bispecific T cell engagers (BiTEs®) are engineered bispecific monoclonal antibodies that target disease cells by directing the host's immune system, more specifically the cytotoxic activity of T cells. BiTEs are fusion proteins consisting of two single-chain variable fragments (scFvs) of different antibodies or amino acid sequences from four different genes, in a single peptide chain of approximately 55 kilodaltons. One scFv binds to T cells via the CD3 receptor, while the other binds to infected cells via a specific molecule.

[0098] Like other bispecific antibodies, but unlike conventional monoclonal antibodies, BiTEs form a link between T cells and target cells. This allows T cells to exert cytotoxic activity against target cells by producing proteins such as perforin and granzymes, regardless of the presence of MHCI or costimulatory molecules. These proteins enter target cells and initiate apoptosis. This action mimics the physiological process observed during T cell attack on infected cells.

[0099] E. Antibody Conjugates The antibodies of the present disclosure can be linked to at least one agent to form an antibody conjugate. The conjugate can be, for example, an antibody conjugated to another proteinaceous, carbohydrate, lipid, or mixed moiety. Such antibody conjugates include, but are not limited to, modifications that involve linking the antibody to one or more polymers. For example, the antibody can be linked to one or more water-soluble polymers. Linking to a water-soluble polymer reduces the likelihood that the antibody will precipitate in an aqueous environment, such as a physiological environment. Those skilled in the art can select a suitable water-soluble polymer based on considerations including, but not limited to, whether the polymer / antibody conjugate will be used to treat a patient, and, if so, the pharmacological profile of the antibody (e.g., half-life, dosage, activity, antigenicity, and / or other factors).

[0100] To increase the efficacy of antibody molecules as diagnostic or therapeutic agents, it is common to link, covalently bond, or complex at least one desired molecule or moiety. Such a molecule or moiety can be, but is not limited to, at least one effector or reporter molecule. Effector molecules include molecules with desired activity, such as cytotoxic activity. Non-limiting examples of effector molecules conjugated to antibodies include toxins, antitumor agents, therapeutic enzymes, radionuclides, antiviral agents, chelators, cytokines, growth factors, and oligo- or polynucleotides. In contrast, a reporter molecule is defined as any moiety that can be detected using an assay. Non-limiting examples of reporter molecules conjugated to antibodies include enzymes, radiolabels, haptens, fluorescent labels, phosphorescent molecules, chemiluminescent molecules, chromophores, photoaffinity molecules, colored particles or ligands, enzymes (e.g., that catalyze colorimetric, fluorescent, or bioluminescent reactions), substrates, solid matrices such as biotin, etc. An antibody can contain one, two, or more of any of these labels.

[0101] Antibody conjugates can be used to deliver cytotoxic agents to target cells. This type of cytotoxic agent can improve antibody-mediated cytotoxicity and includes, for example, moieties such as cytokines that directly or indirectly stimulate cell death, radioisotopes, chemotherapeutic drugs (including prodrugs), bacterial toxins (e.g., Pseudomonas exotoxin, diphtheria toxin, etc.), plant toxins (e.g., ricin, gelonin, etc.), chemical conjugates (e.g., maytansinoid toxin, calicheamicin, etc.), radioconjugates, enzyme conjugates (e.g., RNase conjugates, granzyme antibody-directed enzyme / prodrug therapy), etc.

[0102] Antibody conjugates are also used as diagnostic agents.Antibody diagnostics are generally divided into two categories: those for use in in vitro diagnostics such as various immunoassays, and those for use in in vivo diagnostic protocols generally known as "antibody-directed imaging".Many suitable imaging agents are known in the art, as are their binding methods to antibodies (see, for example, U.S. Patent Nos. 5,021,236, 4,938,948 and 4,472,509).The imaging moiety used can be paramagnetic ions, radioisotopes, fluorescent dyes, NMR detectable substances, MR hyperpolarized molecules, targeted ultrasound bubbles, and X-ray imaging agents.

[0103] Paramagnetic ions contemplated for use as conjugates include chromium(III), manganese(II), iron(III), iron(II), cobalt(II), nickel(II), copper(II), neodymium(III), samarium(III), ytterbium(III), gadolinium(III), vanadium(II), terbium(III), dysprosium(III), holmium(III), and / or erbium(III), with gadolinium being particularly preferred. Ions useful in other contexts, such as X-ray imaging, include, but are not limited to, lanthanum(III), gold(III), lead(II), and bismuth(III). Alternative useful isotopes are those used in hyperpolarized MRI, such as carbon-13 and silica-29.

[0104] Radioisotopes contemplated for use in imaging and radiotherapy as conjugates or covalent bonds include astatine-211, actinium-225, carbon-14, bismuth-212, chromium-51, chlorine-36, cobalt-57, cobalt-58, copper-64, copper-67, europium-152, fluorine-18, gallium-68, gallium-67, gold-198, hydrogen-3, iodine-123, iodine-125, iodine-131, indium-111, iron-52, iron-59, lead-2 Radiolabeled monoclonal antibodies and antibody fragments of the present disclosure may be produced according to methods well known in the art. Radiolabeled monoclonal antibodies and antibody fragments of the present disclosure may be produced according to methods well known in the art. For example, monoclonal antibodies can be iodinated by contact with sodium iodide and / or potassium iodide and a chemical oxidizing agent such as sodium hypochlorite, or an enzymatic oxidizing agent such as lactoperoxidase. Monoclonal antibodies according to the present disclosure can be labeled with technetium-99m by a ligand exchange process, for example, by reducing pertechnetate with a zinc solution, chelating the reduced technetium onto a Sephadex column, and adding the antibody to the column. Alternatively, direct labeling techniques can be used, for example, by incubating pertechnetium, a reducing agent such as SNCl2, a buffer solution such as sodium-potassium phthalate solution, and the antibody.Intermediate functional groups incorporating chelators often used to attach radioisotopes present as metal ions to antibodies are diethylene-triamine-pentaacetic acid (DTPA), ethylenediamine-tetraacetic acid (EDTA), monomeric or dendrimeric 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA), 1,4,7-triazacyclononane-1,4,7-triacetic acid (NOTA), deferoxamine (DFO), or 1-hydroxy-2(1H)-pyridinone derivatives (e.g., 3,4,3-LI(1,2-HOPO) or HOPO).

[0105] Exemplary administration regimens can be found in U.S. Patent Nos. 5,595,721 and 6,015,542, each of which is incorporated herein by reference in its entirety. For example, radiolabeled antibodies can be administered in a single dose designed to deliver a high amount of radioactivity. In such a method, it is contemplated that a radiometric dose of more than 200 cGy is delivered to the patient's entire body. This "high-dose" method requires bone marrow transplantation or some other means to reconstitute the patient's hematopoietic function.

[0106] Therapeutic doses of radiolabeled antibodies can be administered, but the radiation dose received by the patient is limited to a level that is not significantly toxic to bone marrow and does not require bone marrow transplantation or other means to reconstitute hematopoiesis. Effective doses for this method range from 25 to 200 cGy, preferably 25 to 150 cGy, delivered to the patient's entire body.

[0107] Alternatively, a large amount of unlabeled antibody can be administered to a patient in addition to a therapeutic dose of labeled antibody, which can be tailored to deliver a radiometric dose of 5-500 cGy, preferably 25-150 cGy, to the patient's whole body.

[0108] A tracer-labeled amount of antibody may be administered to a patient, followed by imaging of the distribution of the antibody in the patient. After imaging, a radiolabeled antibody treatment regimen is administered, designed to deliver a radiometric dose of 25-500 cGy, preferably 25-150 cGy, to the patient's whole body.

[0109] The above doses are limited to single administrations. Such administrations may be repeated, thus allowing the patient to receive a higher total cumulative dose over the course of imaging and therapy.

[0110] As an example, the amount of radioactivity providing approximately 500 cGy to the whole body is estimated to be approximately 825 mCi of I-131. The amount of radioactivity administered depends in part on the isotope selected. In treatment regimens using I-131, 5-1500 mCi may be used, with preferred amounts being 5-800 mCi, and 5-250 mCi being most preferred. In Y-90 therapy, amounts of radioactivity between 1 and 200 mCi are considered appropriate, with preferred amounts being 1-150 mCi, and 1-100 mCi being most preferred. The preferred means of estimating tissue dose from the amount of administered radioactivity is to perform imaging or other pharmacokinetic regimens using tracer doses to obtain predictive dosimetry estimates.

[0111] "High-dose" protocols, ranging from 200 to 600 cGy (or more) to the whole body, typically require supportive bone marrow replacement protocols, as bone marrow is the tissue where radiation dose is limited due to toxicity. Preferred doses are in the range of 15 to 150 cGy to the whole body, with the most preferred range being 40 to 120 cGy. Using such "low-dose" protocols, bone marrow toxicity is much lower, and the inventors have observed that complete remissions can be achieved without the need for bone marrow replacement therapy.

[0112] Either or both of the diagnostic and therapeutic administrations can be preceded by a "pre-dose" of unlabeled antibody. It is recognized that the effects of pre-dosing in both imaging and therapy vary between patients. Generally, it is preferred that a series of diagnostic imaging administrations be performed using increasing pre-dose of unlabeled antibody. The pre-dose that provides the best ratio of tumor dose to systemic dose is then used before the administration of the radioimmunotherapy dose.

[0113] Fluorescent labels contemplated for use as conjugates include Alexa350, Alexa430, AMCA, BODIPY630 / 650, BODIPY650 / 665, BODIPY-FL, BODIPY-R6G, BODIPY-TMR, BODIPY-TRX, Cascade Blue, Cy3, Cy5,6-FAM, fluorescein isothiocyanate, HEX, 6-JOE, Oregon Green 488, Oregon Green 500, Oregon Green 514, Pacific Blue, REG, rhodamine green, rhodamine red, renographin, ROX, TAMRA, TET, tetramethylrhodamine, and / or Texas Red.

[0114] Additional types of antibodies contemplated by the present disclosure are intended primarily for in vitro use, in which the antibody is linked to a secondary binding ligand and / or enzyme (enzyme tag) that generates a colored product upon contact with a chromogenic substrate. Examples of suitable enzymes include urease, alkaline phosphatase, (horseradish) hydrogen peroxidase, or glucose oxidase. Preferred secondary binding ligands are biotin and avidin and streptavidin compounds.

[0115] Several methods for binding or conjugating antibodies to their conjugate moieties are known in the art. Some binding methods include, for example, the use of metal chelate complexes using organic chelators such as diethylenetriaminepentaacetic anhydride (DTPA), ethylenediaminetetraacetic acid, monomeric or dendrimeric 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA), 1,4,7-triazacyclononane-1,4,7-triacetic acid (NOTA), DFO, HOPO, N-chloro-p-toluenesulfonamide, and / or tetrachloro-3α-6α-diphenylglycouril-3 (U.S. Patent Nos. 4,472,509 and 4,938,948) bound to antibodies. Monoclonal antibodies can also be reacted with enzymes in the presence of coupling agents such as glutaraldehyde or periodate. Conjugates with fluorescein markers are prepared in the presence of these coupling agents or by reaction with isothiocyanates. In U.S. Patent No. 4,938,948, imaging of breast tumors is achieved using monoclonal antibodies, and a detectable imaging moiety is attached to the antibody using a linker such as methyl-p-hydroxybenzimidate or N-succinimidyl-3-(4-hydroxyphenyl)propionate.

[0116] Another known method for site-specific binding of molecules to antibodies involves reacting the antibody with a hapten-based affinity label. Essentially, the hapten-based affinity label reacts with amino acids in the antigen-binding site, thereby destroying this site and blocking specific antigen reaction. However, this may not be advantageous because it results in loss of antigen binding by the antibody conjugate.

[0117] Molecules containing azide groups can also be used to form covalent bonds with proteins via reactive nitrene intermediates generated by low-intensity ultraviolet light. In particular, 2- and 8-azido analogs of purine nucleotides have been used as site-specific optical probes to identify nucleotide-binding proteins in crude cell extracts. 2- and 8-azido nucleotides have also been used to map nucleotide-binding domains in purified proteins and can be used as antibody binders.

[0118] Derivatization of immunoglobulins by selectively introducing sulfhydryl groups into the Fc region of immunoglobulins using reaction conditions that do not alter the antibody binding site is also contemplated. Antibody conjugates produced according to this method have been disclosed and exhibit improved longevity, specificity, and sensitivity (U.S. Patent No. 5,196,066, incorporated herein by reference). Site-specific conjugation of effector or reporter molecules, in which the reporter or effector molecule is conjugated to carbohydrate residues in the Fc region, has also been disclosed in the literature. This approach has been reported to produce promising antibodies for diagnostic and therapeutic use that are currently undergoing clinical evaluation.

[0119] F. Antibody Drug Conjugates Antibody-drug conjugates (ADCs) are a novel class of highly potent biopharmaceuticals designed as targeted therapies for the treatment of people with disease. ADCs are complex molecules composed of an antibody (whole mAb or antibody fragment such as scFv) linked to a biologically active cytotoxic / antiviral payload or drug via a stable chemical linker with a labile bond. Antibody-drug conjugates are examples of bioconjugates and immunoconjugates.

[0120] By combining the unique targeting capabilities of monoclonal antibodies with the cancer-killing potential of cytotoxic drugs, antibody-drug conjugates enable sensitive discrimination between healthy and diseased tissue, meaning that, in contrast to traditional systemic approaches, antibody-drug conjugates target and attack diseased cells, thereby sparing healthy cells from being more severely affected.

[0121] In the development of ADC-based antitumor therapies, anticancer drugs (e.g., cytotoxins or cytotoxins) are conjugated to antibodies that specifically target specific cellular markers (e.g., proteins found only in or on diseased cells). The antibodies target these proteins in the body and attach themselves to the surface of the diseased cells. A biochemical reaction between the antibody and the target protein (antigen) induces a signal in the target cell, which then absorbs or internalizes the antibody along with the cytotoxin. After the ADC is internalized, the cytotoxic agent is released, killing the cell or impairing cell replication. In other cases, the linker is cleavable on the surface of the target cell or early endosome, so complete internalization is not required. Due to this targeting, ideally, the drug has fewer side effects than other agents and a broader therapeutic window.

[0122] A stable linkage between the antibody and the cytotoxic agent is a key aspect of ADCs. Linkers are based on chemical motifs, including disulfides, hydrazones, or peptides (cleavable), or thioethers (non-cleavable), to control the distribution and delivery of cytotoxic agents to target cells. Both cleavable and non-cleavable linkers have been proven safe in preclinical and clinical studies. Brentuximab vedotin contains an enzyme-sensitive cleavable linker that delivers the synthetic antitumor agent monomethyl auristatin E (MMAE), a potent and highly toxic antimicrotubule agent, to human specific CD30-positive malignant cells. Due to its high toxicity, MMAE, which inhibits cell division by blocking tubulin polymerization, cannot be used as a single-agent chemotherapy agent. However, the combination of MMAE linked to an anti-CD30 monoclonal antibody (cAC10, a cell membrane protein of the tumor necrosis factor or TNF receptor), has proven stable in extracellular fluids, cleavable by cathepsins, and safe for treatment. Another approved ADC, trastuzumab emtansine, is a combination of the microtubule inhibitor mertansine (DM-1), a derivative of maytansine, and the antibody trastuzumab (Herceptin® / Genentech / Roche), linked by a stable, non-cleavable linker.

[0123] The availability of better and more stable linkers is changing the function of chemical bonds. The type of linker, cleavable or non-cleavable, confers specific properties to cytotoxic (e.g., anti-cancer) agents. For example, a non-cleavable linker maintains the drug intracellularly. As a result, the entire antibody, linker, and cytotoxic agent enters the target cell, and the antibody is degraded to the amino acid level. The resulting complex—amino acids, linker, and cytotoxic agent—immediately becomes the active drug. In contrast, a cleavable linker is catalyzed by enzymes in or on the host cell, thereby releasing the cytotoxic agent. Commonly used mechanisms for linker cleavage are protease-sensitive, pH-sensitive, and glutathione-sensitive.

[0124] Another type of cleavable linker adds an additional molecule between the cytotoxic agent and the cleavage site. This linker technology allows researchers to create more flexible ADCs without worrying about altering the cleavage kinetics. Researchers are also developing novel methods for peptide cleavage based on Edman degradation. Future directions in ADC development also include the development of site-specific conjugation (TDC) to further improve stability and therapeutic index, as well as alpha-releasing immunoconjugates and antibody-conjugated nanoparticles.

[0125] G. Intrabody In certain embodiments, the antibody is a recombinant antibody suitable for intracellular action; such antibodies are known as "intrabodies." These antibodies can interfere with target function through various mechanisms, such as altering intracellular protein trafficking, interfering with enzyme function, and blocking protein-protein or protein-DNA interactions. In many respects, their structure mimics or resembles the structure of the single-chain and single-domain antibodies discussed above. Indeed, a single transcript / single chain is a key feature that allows intracellular expression in target cells and makes protein transport across the cell membrane more feasible. However, additional features are required. An additional feature that intrabodies may require is a signal for intracellular targeting. Vectors capable of targeting intrabodies (or other proteins) to subcellular regions such as the cytoplasm, nucleus, mitochondria, and ER have been designed and are commercially available (Invitrogen Corp.).

[0126] Two major issues affecting the implementation of intrabody therapeutics are delivery, including cell / tissue targeting, and stability. Regarding delivery, various approaches have been used, such as tissue-directed delivery, the use of cell-type-specific promoters, viral-based delivery, the use of cell-permeable / membrane-translocating peptides, and delivery using exosomes. One delivery method involves the use of lipid-based nanoparticles or exosomes, as taught in U.S. Patent Application Publication No. 2018 / 0177727, the entire contents of which are incorporated by reference. Regarding stability, approaches generally involve either brute-force screening, including methods involving phage display and possibly sequence maturation or development of consensus sequences, or more directed modifications, such as insertion of stabilizing sequences (e.g., Fc regions, chaperone protein sequences, leucine zippers) and disulfide substitutions / modifications.

[0127] H. Antibody Production and Purification Methods for generating monoclonal antibodies generally begin along the same lines as those for preparing polyclonal antibodies. The first step in both of these methods is immunization of a suitable host. As is well known in the art, a given composition for immunization can vary in its immunogenicity. Therefore, it is often necessary to boost the host's immune system, which can be achieved by coupling a peptide or polypeptide immunogen to a carrier. Exemplary and preferred carriers are keyhole limpet hemocyanin (KLH) and bovine serum albumin (BSA). Other albumins, such as ovalbumin, mouse serum albumin, or rabbit serum albumin, can also be used as carriers. Means for conjugating polypeptides to carrier proteins are known in the art and include glutaraldehyde, m-maleimidobenocoyl-N-hydroxysuccinimide ester, carbodiimide, and bis-biazotized benzidine. As is well known in the art, the immunogenicity of a particular immunogen composition can be enhanced by the use of nonspecific stimulators of the immune response, known as adjuvants. Exemplary and preferred adjuvants in animals include complete Freund's adjuvant (a nonspecific stimulator of the immune response containing killed Mycobacterium tuberculosis), incomplete Freund's adjuvant, and aluminum hydroxide adjuvant. In humans, adjuvants include alum, CpG, MFP59, and combinations of immunostimulatory molecules ("adjuvant systems," e.g., AS01 or AS03). Additional experimental forms of vaccination to induce antigen-specific B cells are possible, including nanoparticle vaccines, or gene-encoded antigens delivered as DNA or RNA genes in physical delivery systems (such as lipid nanoparticles or gold biolistic beads), delivered by needle, gene gun, or transcutaneous electroporation device.The antigen gene can also be carried so as to be encoded by a replication-competent or defective viral vector such as an adenovirus, adeno-associated virus, poxvirus, herpesvirus, or alphavirus replicon, or alternatively a virus-like particle.

[0128] Methods for generating hybrids between antibody-producing cells and myeloma cells typically involve mixing somatic cells and myeloma cells at a 2:1 ratio in the presence of one or more agents (chemical or electrical) that promote cell membrane fusion, although the ratio can vary from approximately 20:1 to approximately 1:1. In some cases, transformation of human B cells with Epstein-Barr virus (EBV) as an initial step increases the size of the B cells and enhances fusion with relatively large myeloma cells. The efficiency of EBV transformation is enhanced by using CpG and Chk2 inhibitors in the transformation medium. Alternatively, human B cells can be activated by co-culture with a transduced cell line expressing CD40 ligand (CD154) in a medium containing additional soluble factors such as IL-21 and human B cell-activating factor (BAFF), a type II member of the TNF superfamily. Fusion methods using Sendai virus or polyethylene glycol (PEG) are also known. Electrically induced fusion is also suitable. The fusion procedure typically involves approximately 1 × 10 -6 ~1×10 -8Although viable hybrids are generated at a low frequency, optimized procedures can achieve fusion efficiencies approaching 1 in 200. However, this relatively low fusion efficiency does not pose a problem because surviving fused hybrids differentiate from the parental injected cells (especially the injected myeloma cells, which would normally continue to divide indefinitely) by culturing them in selective media. Selective media generally contain drugs that block de novo synthesis of nucleotides in tissue culture media. Exemplary and preferred drugs are aminopterin, methotrexate, and azaserine. Aminopterin and methotrexate block de novo synthesis of both purines and pyrimidines, whereas azaserine blocks only purine synthesis. When aminopterin or methotrexate is used, the medium is supplemented with hypoxanthine and thymidine as a source of nucleotides (HAT medium). When azaserine is used, the medium is supplemented with hypoxanthine. If the B cell source is an EBV-transformed human B cell line, ouabain is added to eliminate EBV-transformed cell lines that have not fused to myeloma.

[0129] The preferred selective medium is HAT or HAT supplemented with ouabain. Only cells capable of operating the nucleotide salvage pathway can survive in HAT medium. Myeloma cells lack key enzymes in the salvage pathway, such as hypoxanthine phosphoribosyltransferase (HPRT), and cannot survive. B cells can operate this pathway, but they have a limited lifespan in culture and generally die within about two weeks. Therefore, the only cells that can survive in selective medium are those hybrids formed from myeloma and B cells. When the source of B cells used for fusion is a lineage of EBV-transformed B cells, as here, ouabain can also be used for drug selection of the hybrid, as EBV-transformed B cells are susceptible to drug killing, and the myeloma partner used is selected to be ouabain-resistant.

[0130] Culturing provides a population of hybridomas from which specific hybridomas can be selected. Hybridoma selection is typically performed by culturing cells by single-clone dilution in microtiter plates, followed by testing individual clonal supernatants (after approximately 2–3 weeks) for the desired reactivity. Assays should be sensitive, simple, and rapid, such as radioimmunoassays, enzyme immunoassays, cytotoxicity assays, plaque assays, or dot immunobinding assays. Selected hybridomas are then serially diluted or single-cell sorted by flow cytometry sorting, cloned into individual antibody-producing cell lines, and the clones can then be propagated indefinitely to provide monoclonal antibodies. Cell lines can be utilized for monoclonal antibody production in two basic ways: A sample of the hybridomas can be injected (often intraperitoneally) into an animal (e.g., a mouse). Optionally, the animal is primed with a hydrocarbon, particularly an oil such as pristane (tetramethylpentadecane), prior to injection. When human hybridomas are used in this method, they are optimally injected into immunocompromised mice, such as SCID mice, to prevent tumor rejection. The injected animals develop tumors that secrete the specific monoclonal antibodies produced by the fused cell hybrids. The animal's body fluids, such as serum or ascites, can then be harvested to provide high concentrations of monoclonal antibodies. Individual cell lines can also be cultured in vitro, and the monoclonal antibodies are naturally secreted into the culture medium, where they can be easily obtained in high concentrations. Alternatively, human hybridoma cell lines can be used in vitro to produce immunoglobulins in the cell supernatant. Cell lines can be adapted to growth in serum-free medium to optimize the ability to recover highly pure human monoclonal immunoglobulins.

[0131] Hybridomas are cultured, then the cells are lysed and total RNA is extracted. Random hexamers are used with RT to generate cDNA copies of the RNA, and PCR is then performed using a multiplexed mixture of PCR primers expected to amplify the entire human variable gene sequence. PCR products can be cloned into the pGEM-T Easy vector and then sequenced by automated DNA sequencing using standard vector primers. Binding and neutralization assays can be performed using antibodies collected from hybridoma supernatants and purified by FPLC using a protein G column.

[0132] Recombinant full-length IgG antibodies can be produced by subcloning the heavy and light chain Fv DNA from the cloning vector into an IgG plasmid vector, transfecting 293 (e.g., Freestyle) or CHO cells, and the antibody can be collected and purified from the 293 or CHO cell supernatant. Other suitable host cell systems include bacteria such as E. coli, insect cells (S2, Sf9, Sf29, High Five), plant cells (e.g., tobacco, with or without engineering for human-like glycans), algae, or various non-human transgenic contexts such as mouse, rat, goat, or cow.

[0133] Expression of nucleic acids encoding antibodies is contemplated for both subsequent antibody purification and host immunization. The antibody-encoding sequence can be RNA, such as native or modified RNA. Modified RNAs are specific chemical modifications that confer increased stability and reduced immunogenicity to mRNA, thereby facilitating the expression of therapeutically important proteins. For example, N1-methyl-pseudouridine (N1mψ) outperforms several other nucleoside modifications and their combinations in terms of translational potency. In addition to switching off immune / eIF2α phosphorylation-dependent inhibition of translation, the incorporated N1mψ nucleotide dramatically alters the kinetics of the translation process by increasing ribosome pausing and mRNA density. The increased ribosome load of modified mRNAs makes them more permissive by favoring either ribosome recycling or de novo ribosome recruitment to the same mRNA. Such modifications can be used to enhance antibody expression in vivo after RNA inoculation. Whether native or modified, the RNA can be delivered as naked RNA or in a delivery vehicle such as a lipid nanoparticle.

[0134] Alternatively, DNA encoding an antibody can be used for the same purpose. The DNA is contained in an expression cassette that contains a promoter that is active in the host cell in which it is designed. The expression cassette is effectively contained in a replicable vector, such as a conventional plasmid or minivector. The vector includes viral vectors such as poxvirus, adenovirus, herpesvirus, adeno-associated virus, and lentivirus. Replicons encoding antibody genes, such as alphavirus replicons based on VEE virus or Sindbis virus, are also contemplated. Such vectors can be delivered by needles through intramuscular, subcutaneous, or intradermal routes, or by transcutaneous electroporation if in vivo expression is desired.

[0135] Alternatively, monoclonal antibodies can be generated using a molecular cloning approach. Single B cells labeled with the antigen of interest can be physically sorted using paramagnetic bead selection or flow cytometry, and then RNA can be isolated from the single cells and antibody genes can be amplified by RT-PCR. Alternatively, a population of antigen-specific bulk-sorted cells can be separated into matched heavy and light chain variable genes recovered from single cells using microvesicles and the physical binding of heavy and light chain amplicons, or common barcoding of heavy and light chain genes from vesicles. Matched heavy and light chain genes from single cells can also be obtained from a population of antigen-specific B cells by treating the cells with RT-PCR primers and cell-penetrating nanoparticles bearing barcodes to mark transcripts with one barcode per cell. Antibody variable genes can also be isolated by RNA extraction of hybridoma lines and antibody genes obtained by RT-PCR and cloned into immunoglobulin expression vectors. Alternatively, combinatorial immunoglobulin phagemid libraries are prepared from RNA isolated from cell lines, and phagemids expressing appropriate antibodies are selected by panning using viral antigens. The advantage of this approach over traditional hybridoma techniques is approximately 10 4 The advantages of this approach are that twice as many antibodies can be produced and screened in one go, and new specificities can be generated by combining heavy and light chains, further increasing the chances of finding a suitable antibody.

[0136] Other U.S. patents, each incorporated herein by reference, that teach the production of antibodies useful in the present disclosure include U.S. Pat. No. 5,565,332, which describes the production of chimeric antibodies using a combinatorial approach; U.S. Pat. No. 4,816,567, which describes recombinant immunoglobulin preparations; and U.S. Pat. No. 4,867,973, which describes antibody-therapeutic agent conjugates.

[0137] Monoclonal antibodies produced by any means may be purified, if necessary, using filtration, centrifugation, and various chromatographic methods such as FPLC or affinity chromatography. Fragments of the monoclonal antibodies of the present disclosure can be obtained from purified monoclonal antibodies by methods including digestion with enzymes such as pepsin or papain, and / or by cleavage of disulfide bonds by chemical reduction. Alternatively, monoclonal antibody fragments encompassed by the present disclosure can be synthesized using an automated peptide synthesizer.

[0138] The antibody of the present disclosure can be purified. As used herein, the term "purified" is intended to refer to a composition that can be isolated from other components, and the protein is purified to any degree compared to its naturally obtainable state. Thus, a purified protein also refers to a protein that is free from the environment in which it may naturally exist. When the term "substantially purified" is used, this designation refers to a composition in which the protein or peptide forms the major component of the composition, such as constituting about 50%, about 60%, about 70%, about 80%, about 90%, about 95% or more of the protein in the composition.

[0139] Protein purification techniques are well known to those skilled in the art. These techniques include, at one level, crude fractionation of the cellular environment into polypeptide and non-polypeptide fractions. After separating the polypeptide from other proteins, the polypeptide of interest can be further purified using chromatographic and electrophoretic techniques to achieve partial or complete purification (or purification to homogeneity). Analytical methods particularly suitable for preparing pure peptides include ion exchange chromatography, exclusion chromatography, polyacrylamide gel electrophoresis, and isoelectric focusing. Other methods for protein purification include precipitation using ammonium sulfate, PEG, antibodies, etc., or by heat denaturation, followed by centrifugation; gel filtration, reverse phase, hydroxylapatite, and affinity chromatography; and combinations of such and other techniques.

[0140] When purifying the antibodies of the present disclosure, it may be desirable to express the polypeptide in a prokaryotic or eukaryotic expression system and extract the protein using denaturing conditions. The polypeptide can be purified from other cellular components using an affinity column that binds to the tagged portion of the polypeptide. As is generally known in the art, the order in which various purification steps are performed can be changed, and certain steps can be omitted, and still result in a suitable method for preparing a substantially purified protein or peptide.

[0141] Generally, whole antibodies are fractionated using an agent that binds to the Fc portion of the antibody (i.e., Protein A). Alternatively, antigen can be used to simultaneously purify and select suitable antibodies. Such methods often utilize a selection agent bound to a support, such as a column, filter, or beads. The antibody is bound to the support, contaminants are removed (e.g., washed away), and the antibody is released by applying conditions (salt, heat, etc.).

[0142] Various methods for quantifying the degree of purification of a protein or peptide will be known to those of skill in the art in light of the present disclosure. These include, for example, determining the specific activity of an active fraction or assessing the amount of polypeptide within a fraction by SDS / PAGE analysis. Another way to assess the purity of a fraction is to calculate the specific activity of the fraction and compare it to the specific activity of the initial extract to calculate the degree of purity. The actual units used to express the amount of activity will, of course, depend on the particular assay technique chosen to follow purification, as well as whether the expressed protein or peptide exhibits detectable activity.

[0143] It is known that the migration of polypeptides can vary, sometimes significantly, under different conditions of SDS / PAGE, and therefore it will be understood that the apparent molecular weight of purified or partially purified expression products may vary under different electrophoretic conditions.

[0144] I. Antibody Modification The sequence of the antibody may be modified for various reasons, such as improved expression, improved cross-reactivity, or reduced off-target binding. The modified antibody may be made by any technique known to those skilled in the art, including expression by standard molecular biology techniques or chemical synthesis of polypeptides.

[0145] For example, one may wish to make modifications such as introducing conservative changes into an antibody molecule. When making such changes, the hydropathic amino acid index can be taken into consideration. The importance of the hydropathic amino acid index in conferring interactive biological function to a protein is generally understood in the art (Kyte and Doolittle, 1982). It is recognized that the relative hydropathic properties of amino acids contribute to the secondary structure of the resulting protein, which in turn determines the interaction of the protein with other molecules, such as enzymes, substrates, receptors, DNA, antibodies, antigens, etc.

[0146] Substitution of similar amino acids can be effectively made based on hydrophilicity. U.S. Pat. No. 4,554,101, incorporated herein by reference, states that the greatest local average hydrophilicity of a protein, when governed by the hydrophilicity of its neighboring amino acids, correlates with the biological properties of the protein. As described in detail in U.S. Pat. No. 4,554,101, hydrophilicity values ​​are assigned to amino acid residues, including basic amino acids: arginine (+3.0), lysine (+3.0), and histidine (-0.5); acidic amino acids: aspartic acid (+3.0±1), glutamic acid (+3.0±1), asparagine (+0.2), and glutamine (+0.2); hydrophilic non-ionic amino acids: serine (+0.3), asparagine (+0.2). , glutamine (+0.2), and threonine (-0.4); sulfur-containing amino acids: cysteine ​​(-1.0) and methionine (-1.3); hydrophobic non-aromatic amino acids: valine (-1.5), leucine (-1.8), isoleucine (-1.8), proline (-0.5±1), alanine (-0.5), and glycine (0); hydrophobic aromatic amino acids: tryptophan (-3.4), phenylalanine (-2.5), and tyrosine (-2.3).

[0147] An amino acid can be substituted with another amino acid having a similar hydrophilicity and resulting in a biologically or immunologically altered protein. In such changes, substitution of amino acids with hydrophilicity values ​​within ±2 is preferred, those within ±1 are particularly preferred, and those within ±0.5 are even more particularly preferred.

[0148] Amino acid substitutions are generally based on the relative similarity of the amino acid side-chain substituents, e.g., their hydrophobicity, hydrophilicity, charge, size, etc. Exemplary substitutions that take into account various characteristics such as those mentioned above are well known to those of skill in the art and include arginine for lysine, glutamic acid for aspartic acid, serine for threonine, glutamine for asparagine, and valine for leucine and isoleucine.

[0149] The present disclosure also contemplates isotype modification. By modifying the Fc region to have a different isotype, different functions can be achieved. For example, changing to IgG1 can increase antibody-dependent cellular cytotoxicity, switching to class A can improve tissue distribution, and switching to class M can improve binding valency.

[0150] For example, an Fc region of an antibody can be engineered with altered effector functions by modifying C1q binding and / or FcγR binding, thereby altering CDC and / or ADCC activity. An "effector function" is involved in activating or reducing a biological activity (e.g., in a subject). Examples of effector functions include, but are not limited to, C1q binding, complement-dependent cytotoxicity (CDC), Fc receptor binding, antibody-dependent cell-mediated cytotoxicity (ADCC), phagocytosis, down-regulation of cell surface receptors (e.g., B cell receptors, BCR), and the like. Such effector functions may require binding of the Fc region to a binding domain (e.g., an antibody variable domain) and can be assessed using various assays (e.g., Fc binding assays, ADCC assays, CDC assays, etc.).

[0151] For example, a variant Fc region of an antibody can be generated that has improved C1q binding and improved FcγRIII binding (e.g., has both improved ADCC activity and improved CDC activity). Alternatively, if reduced or eliminated effector function is desired, the variant Fc region can be engineered with reduced CDC activity and / or reduced ADCC activity. In other embodiments, only one of these activities can be increased, and optionally, the other activity can be reduced as well (e.g., generating an Fc region variant with improved ADCC activity but reduced CDC activity, or vice versa).

[0152] The isolated monoclonal antibody, or antigen-binding fragment thereof, can contain substantially homogeneous glycans that do not contain sialic acid, galactose, or fucose. The substantially homogeneous glycans can be covalently attached to the heavy chain constant region.

[0153] Monoclonal antibodies can have novel Fc glycosylation patterns. Glycosylation of the Fc region is typically either N-linked or O-linked. N-linked refers to the attachment of a carbohydrate moiety to the side chain of an asparagine residue. O-linked glycosylation refers to the attachment of one of the sugars N-acetylgalactosamine, galactose, or xylose to a hydroxyamino acid, most commonly serine or threonine, although 5-hydroxyproline or 5-hydroxylysine can also be used. The recognition sequences for enzymatic attachment of the carbohydrate moiety to the asparagine side chain peptide sequence are asparagine-X-serine and asparagine-X-threonine, where X is any amino acid except proline. Thus, the presence of either of these peptide sequences in a polypeptide creates a potential glycosylation site.

[0154] The glycosylation pattern can be modified, for example, by deleting one or more glycosylation sites present in the polypeptide and / or adding one or more glycosylation sites that are not present in the polypeptide. Addition of a glycosylation site to the Fc region of an antibody is conveniently achieved by altering the amino acid sequence to include one or more of the above tripeptide sequences (for N-linked glycosylation sites). An exemplary glycosylation variant has an amino acid substitution of residue Asn297 of the heavy chain. Alterations can also be made by adding or substituting one or more serine or threonine residues into the original polypeptide sequence (for O-linked glycosylation sites). Furthermore, one of the glycosylation sites can be removed by changing Asn297 to Ala.

[0155] The isolated monoclonal antibody, or antigen-binding fragment thereof, may be present in a substantially homogeneous composition represented by the GNGN or G1 / G2 glycoforms and exhibit increased binding affinity to Fc gamma RI and Fc gamma RIII compared to glycoforms that do not have substantially homogeneous GNGN glycoforms and contain G0, G1F, G2F, GNF, GNGNF, or GNGNFX. Fc glycosylation plays an important role in the antiviral and anticancer properties of therapeutic mAbs. Removal of core fucose dramatically improves the ADCC activity of mAbs mediated by natural killer (NK) cells but appears to have the opposite effect on ADCC activity of polymorphonuclear cells (PMNs).

[0156] The isolated monoclonal antibody, or its antigen-binding fragment, can be expressed in cells expressing beta(1,4)-N-acetylglucosaminyltransferase III (GnTIII), whereby GnTIII adds GlcNAc to the antibody. Methods for producing antibodies in this manner are provided in WO / 9954342 and WO / 03011878. Cell lines can be modified using genome editing techniques such as clustered regularly interspaced short palindromic repeats (CRISPR) to enhance, reduce, or eliminate specific post-translational modifications, such as glycosylation. For example, CRISPR technology can be used to eliminate genes encoding glycosylation enzymes in 293 or CHO cells used to express monoclonal antibodies.

[0157] Antibody variable gene sequences obtained from human B cells can be engineered to enhance their manufacturability and safety. Potential protein sequence trends can be identified by searching for sequence motifs associated with sites containing: 1) unpaired Cys residue, 2) N-linked glycosylation, 3) Asn deamidation, 4) Asp isomerization, 5) SYE cutting, 6) Met oxidation, 7) Trp oxidation, 8) N-terminal glutamic acid, 9) integrin binding, 10) CD11c / CD18 binding, or 11) Fragmentation Such motifs can be eliminated by modifying the synthetic gene containing the cDNA encoding the antibody.

[0158] Antibodies can be engineered to enhance solubility. For example, some hydrophilic residues, such as aspartic acid, glutamic acid, and serine, contribute significantly more favorably to protein solubility than other hydrophilic residues, such as asparagine, glutamine, threonine, lysine, and arginine.

[0159] Deep sequencing of the B cell repertoire of human B cells from blood donors has been extensively performed. Sequence information for a significant portion of the human antibody repertoire facilitates the statistical evaluation of antibody sequence features common in healthy humans. Knowledge of antibody sequence features in the Human Recombinant Antibody Variable Gene Reference Database allows for the estimation of position-specific "human similarity" (HL) of antibody sequences. HL has been shown to be useful in the development of antibodies for clinical use, such as therapeutic antibodies or antibodies as vaccines. The goal is to increase the human similarity of antibodies to reduce potential adverse effects and anti-antibody immune responses that can lead to a significant reduction in the efficacy of antibody drugs or induce serious health consequences. By assessing the antibody characteristics of the combined antibody repertoire of three healthy human blood donors, totaling approximately 400 million sequences, a new "relative human similarity" (rHL) score can be created that focuses on the hypervariable regions of antibodies. The rHL score allows for easy differentiation between human (positive score) and non-human sequences (negative score). Antibodies can be engineered to eliminate residues that are uncommon in the human repertoire.

[0160] J. Antibody Characterization Antibodies according to the present disclosure can be defined, in a first example, by their binding specificity. One skilled in the art can determine whether a given antibody falls within the scope of the present claims by evaluating the binding specificity / affinity of such an antibody using techniques well known to those skilled in the art. For example, the epitope to which a given antibody binds may consist of a single contiguous sequence of three or more (e.g., 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20) amino acids located within an antigen molecule (e.g., a linear epitope within a domain). Alternatively, the epitope may consist of multiple non-contiguous amino acids (or amino acid sequences) located within an antigen molecule (e.g., a conformational epitope).

[0161] Various techniques known to those skilled in the art can be used to determine whether an antibody "interacts with one or more amino acids" within a polypeptide or protein. Exemplary techniques include routine cross-blocking assays, such as those described in Antibodies, Harlow and Lane (Cold Spring Harbor Press, Cold Spring Harbor, NY). Cross-blocking can be measured by various binding assays, such as ELISA, biolayer interferometry, or surface plasmon resonance. Other methods include alanine scanning mutation analysis, peptide blot analysis (Reineke (2004) Methods Mol. Biol. 248:443-63), peptide truncation analysis, high-resolution electron microscopy using single-particle reconstruction, cryoEM, or tomography, crystallography, and NMR analysis. In addition, methods such as epitope excision, epitope extraction, and chemical modification of antigens can be used (Tomer (2000) Prot. Sci. 9:487-496). Another method that can be used to identify amino acids in a polypeptide with which an antibody interacts is hydrogen / deuterium exchange detected by mass spectrometry. Generally speaking, hydrogen / deuterium exchange involves deuterium-labeling a protein of interest and then binding an antibody to the deuterium-labeled protein. The protein / antibody complex is then transferred to water, and exchangeable protons in amino acids protected by the antibody complex undergo back-exchange from deuterium to hydrogen at a slower rate than exchangeable protons in amino acids that are not part of the interface. As a result, amino acids that form part of the protein / antibody interface can retain deuterium and therefore exhibit a relatively higher mass than amino acids that are not included in the interface. After dissociation of the antibody, the target protein is subjected to protease cleavage and mass spectrometry, thereby revealing deuterium-labeled residues corresponding to the specific amino acids with which the antibody interacts. See, for example, Ehring (1999) Analytical Biochemistry 267:252-259; Engen and Smith (2001) Anal. Chem. 73:256A-265A.

[0162] The term "epitope" refers to a site on an antigen to which B cells and / or T cells respond. B cell epitopes can be formed from both contiguous amino acids or noncontiguous amino acids juxtaposed by tertiary folding of a protein. Epitopes formed from contiguous amino acids are typically retained upon exposure to denaturing solvents, whereas epitopes formed by tertiary folding are typically lost upon treatment with denaturing solvents. Epitopes typically contain at least three, more commonly at least five, or 8-10 amino acids in a unique spatial conformation.

[0163] Modification-assisted profiling (MAP), also known as antigen structure-based antibody profiling (ASAP), is a method for classifying multiple monoclonal antibodies directed against the same antigen according to the similarity of each antibody's binding profile to chemically or enzymatically modified antigen surfaces (see US2004 / 0101920, specifically incorporated herein by reference in its entirety). Each category may reflect a unique epitope that is either distinctly different from or partially overlaps with the epitopes represented by other categories. This technique allows for rapid filtering of genetically identical antibodies, thereby focusing characterization on genetically distinct antibodies. When applied to hybridoma screening, MAP can facilitate the identification of rare hybridoma clones producing monoclonal antibodies with desired characteristics. MAP can be used to classify the antibodies of the present disclosure into groups of antibodies that bind to different epitopes.

[0164] The present disclosure includes antibodies that can bind to the same epitope or a portion of an epitope. Whether an antibody binds to the same epitope as a reference antibody or competes for binding with a reference antibody can be easily determined using routine methods known in the art. For example, to determine whether a test antibody binds to the same epitope as a reference antibody, the reference antibody is bound to a target under saturating conditions. The ability of the test antibody to bind to the target molecule is then evaluated. If the test antibody can bind to the target molecule after saturation binding with the reference antibody, it can be concluded that the test antibody binds to a different epitope from the reference antibody. On the other hand, if the test antibody cannot bind to the target molecule after saturation binding with the reference antibody, the test antibody may bind to the same epitope as the epitope bound by the reference antibody.

[0165] In another embodiment, antibodies can be defined by their variable sequences, including additional "framework" regions. These are provided in Table 4, which represents the complete variable regions. Additionally, antibody sequences can be varied from these sequences, optionally using methods discussed in more detail below. For example, nucleic acid sequences can be varied from those shown above such that (a) the variable regions are separated from the light and heavy chain constant domains; (b) the nucleic acid is varied from those shown above but does not affect the residues encoded thereby; (c) the nucleic acid is varied from those shown above by a given percentage, e.g., 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% homology; or (d) the nucleic acid is varied from those shown above by about 0.02% or less at temperatures between about 50° C. and about 70° C. (e) the amino acids may vary from those set forth above by a given percentage, e.g., 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% homology; or (f) the amino acids may vary from those set forth above by allowing for conservative substitutions.

[0166] When comparing polynucleotide and polypeptide sequences, two sequences are said to be "identical" if the nucleotide or amino acid sequences in the two sequences are the same when aligned for maximum correspondence, as described below. Comparison between two sequences is typically performed by comparing the sequences over a comparison span to identify and compare local regions of sequence similarity. As used herein, "comparison span" refers to a segment of at least about 20 contiguous positions, typically 30 to about 75, 40 to about 50, over which a sequence can be compared to a reference sequence of the same number of contiguous positions after optimal alignment of the two sequences.

[0167] Optimal alignment of sequences for comparison can be performed using the Megalign program in the Lasergene suite of bioinformatics software (DNASTAR, Inc., Madison, Wis.) with default parameters. Alternatively, optimal alignment of sequences for comparison can be performed by the local identity algorithm of Smith and Waterman (1981) Add. APL. Math 2:482, by the identity alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for identity method of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. USA 85:2444, by computerized implementations of these algorithms (GAP, BESTFIT, BLAST, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group (GCG), 575 Science Dr., Madison, Wis.), or by inspection.

[0168] One specific example of an algorithm suitable for determining percent sequence identity and sequence similarity is BLAST and BLAST 2.0, which are described in Altschul et al. (1977) Nucl. Acids Res. 25:3389-3402 and Altschul et al. (1990) J. Mol. Biol. 215:403-410, respectively. BLAST and BLAST 2.0 can be used, for example, with the parameters described herein, to determine percent sequence identity for the polynucleotides and polypeptides of the present disclosure. Software for performing BLAST analysis is publicly available through the National Center for Biotechnology Information. The rearranged nature of antibody sequences and the variable length of each gene necessitates multiple BLAST searches for a single antibody sequence. Furthermore, manual assembly of different genes is difficult and error-prone. The sequence analysis tool IgBLAST (world-wide-web at ncbi.nlm.nih.gov / igblast / ) identifies matches to germline V, D, and J genes, details on rearrangement junctions, delineation of IgV domain framework regions, and complementarity-determining regions. IgBLAST can analyze nucleotide or protein sequences and can process sequences in batches, allowing simultaneous searches against germline gene databases and other sequence databases, minimizing the chance of missing the best matching germline V gene.

[0169] In one approach, "percentage of sequence identity" is determined by comparing two optimally aligned sequences over a comparison span of at least 20 positions, where the portion of the polynucleotide or polypeptide sequence in the comparison span may contain 20 percent or less, typically 5-15 percent, or 10-12 percent, additions or deletions (i.e., gaps) compared to the reference sequence (not including additions or deletions) due to optimal alignment of the two sequences. The percentage is calculated by determining the number of positions where the same nucleic acid base or amino acid residue occurs in both sequences to obtain the number of matched positions, dividing the number of matched positions by the total number of positions in the reference sequence (i.e., the span size), and multiplying the result by 100 to obtain the percentage of sequence identity.

[0170] Another way to further define antibodies is as a "derivative" of any of the antibodies and antigen-binding fragments thereof provided herein. Derivative antibodies or antibody fragments may be modified by chemical modification using techniques known to those skilled in the art, including, but not limited to, specific chemical cleavage, acetylation, formulation, and metabolic synthesis of tunicamycin. In one embodiment, an antibody derivative has similar or identical function as the parent antibody. In another embodiment, an antibody derivative exhibits altered activity compared to the parent antibody. For example, a derivative antibody (or fragment thereof) may bind to its epitope more tightly or be more resistant to proteolysis than the parent antibody.

[0171] The term "derivative" refers to an antibody or antigen-binding fragment thereof that immunospecifically binds to an antigen but contains one, two, three, four, five, or more amino acid substitutions, additions, deletions, or modifications compared to the "parent" (or wild-type) molecule. Such amino acid substitutions or additions may introduce naturally occurring (i.e., DNA-encoded) or non-naturally occurring amino acid residues. The term "derivative" encompasses variants, e.g., having altered CH1, hinge, CH2, CH3, or CH4 regions, thereby forming antibodies with variant Fc regions that exhibit, e.g., enhanced or impaired effector or binding characteristics. The term "derivative" further encompasses non-amino acid modifications, such as amino acids that may be glycosylated (e.g., having altered mannose, 2-N-acetylglucosamine, galactose, fucose, glucose, sialic acid, 5-N-acetylneuraminic acid, 5-glycolneuraminic acid, etc. content), acetylated, pegylated, phosphorylated, amidated, derivatized with known protecting / blocking groups, proteolytic cleavage, linked to cellular ligands or other proteins, etc. In some embodiments, the altered carbohydrate modification modulates one or more of antibody solubilization, promoting intracellular trafficking and secretion of the antibody, promoting antibody assembly, conformational integrity, and antibody-mediated effector function. In certain embodiments, the altered carbohydrate modification enhances antibody-mediated effector function compared to an antibody lacking the carbohydrate modification. Carbohydrate modifications that result in altered antibody-mediated effector function are well known in the art.

[0172] The biophysical properties of antibodies can be determined. Elevated temperatures can be used to unfold the antibody, and the apparent mean melting temperature can be used to determine relative stability. Differential scanning calorimetry (DSC) measures the heat capacity, C p DSC measures the heat required to warm it (the heat per degree required to warm it) as a function of temperature. Using DSC, the thermal stability of antibodies can be tested. DSC data for mAbs shows that it sometimes resolves the unfolding of individual domains within the mAb structure, resulting in up to three peaks in the thermogram (Fab, C). H 2, and CHThis is of particular interest because the unfolding of the Fab domain typically produces the strongest peak. The DSC profiles and relative stability of the Fc portion show characteristic differences among human IgG1, IgG2, IgG3, and IgG4 subclasses (Garber and Demarest, Biochem. Biophys. Res. Commun. 355, 751-757, 2007). Circular dichroism (CD) can also be used to determine the apparent mean melting temperature, which is performed using a CD spectrometer. Far-UV CD spectra are measured for antibodies from 200 to 260 nm with 0.5 nm increments. The final spectrum can be determined as the average of 20 accumulations. Residue ellipticity values ​​can be calculated after background subtraction. Thermal unfolding of antibodies (0.1 mg / mL) can be monitored at 235 nm from 25 to 95 °C and a heating rate of 1 °C / min. Dynamic light scattering (DLS) can be used to assess aggregation propensity. DLS can be used to characterize the size of various particles, including proteins. If the system is not size-dispersed, the average effective diameter of the particles can be determined. This measurement depends on the particle core size, the size of the surface structures, and the particle concentration. DLS essentially measures the variation in scattered light intensity by particles, allowing the particle's diffusion coefficient to be determined. The DLS software of commercially available DLS instruments displays particle populations with different diameters. Stability testing can be conveniently performed using DLS. DLS measurements of a sample can indicate whether particles aggregate over time or with temperature changes by determining whether the hydrodynamic radius of the particles increases. If particles aggregate, a larger population of particles with a larger radius will be indicated. Temperature-dependent stability can be analyzed by controlling the temperature in situ. Capillary electrophoresis (CE) techniques include a proven methodology for characterizing antibody stability. The iCE approach can be used to resolve antibody protein charge variants resulting from deamidation, C-terminal lysine, sialylation, oxidation, glycosylation, and any other modification to the protein that can alter the protein's pI.Each expressed antibody protein can be assessed by high-throughput free-solution isoelectric focusing (IEF) in a capillary column (cIEF) using the Protein Simple Maurice instrument. Whole-column UV absorbance detection can be performed every 30 seconds for real-time monitoring of molecules focused on their isoelectric points (pIs). This approach combines the high resolution of traditional gel-IEF with the quantification and automation benefits of column-based separations, eliminating the need for a mobilization step. This technique provides reproducible quantitative analysis of the identity, purity, and heterogeneity profile of expressed antibodies. Results identify charge heterogeneity and molecular size in antibodies in both absorbance and native fluorescence detection modes, with a detection sensitivity down to 0.7 μg / mL.

[0173] The intrinsic solubility score of an antibody sequence can be determined. This can be calculated using CamSol Intrinsic (Sormanni et al. J. Mol. Biol. 427, 478-490, 2015). The amino acid sequence of residues 95-102 (Kabat numbering) in HCDR3 of each antibody fragment, such as an ScFv, can be evaluated via an online program to calculate a solubility score. Alternatively, solubility can be determined using laboratory techniques. Various techniques exist, including adding lyophilized protein to a solution until the solution is saturated and the solubility limit is reached, or concentrating by ultrafiltration in a microconcentrator with a suitable molecular weight cutoff. The simplest method is the induction of an amorphous precipitate, which measures protein solubility using a method involving protein precipitation using ammonium sulfate (Trevino et al. J. Mol. Biol. 366:449-460, 2007). Ammonium sulfate precipitation provides rapid and accurate information on relative solubility values. Ammonium sulfate precipitation produces a precipitation solution with well-defined aqueous and solid phases and requires a relatively small amount of protein. Solubility measurements performed using ammonium sulfate induction of amorphous precipitates can also be easily performed at different pH values. Protein solubility is highly dependent on pH, and pH is considered to be the most important extrinsic factor affecting solubility.

[0174] Although it is generally thought that autoreactive clones should be eliminated during ontogeny by negative selection, it has become clear that many naturally occurring human antibodies with autoreactivity persist in the mature repertoire, and that autoreactivity can enhance the antiviral function of many antibodies against pathogens. It has been noted that the HCDR3 loop in antibodies during early B cell development is often rich in positive charges and exhibits an autoreactive pattern (Wardemann et al. Science, 301, 1374-1377, 2003). A given antibody can be tested for autoreactivity by assessing the level of binding to cells of human origin in microscopy (using adherent HeLa or HEp-2 epithelial cells) and flow cytometry cell surface staining (using suspension Jurkat T cells and 293S human embryonic kidney cells). Autoreactivity can also be investigated using assessment of tissue binding in tissue arrays.

[0175] III. Chimeric Antigen Receptors Chimeric antigen receptor (CAR) molecules are recombinant fusion proteins distinguished by their ability to both bind antigens and transduce activation signals via immunoreceptor activation motifs (ITAMs) present in their cytoplasmic tails to activate genetically engineered immune effector cells in killing, proliferation, and cytokine production. Receptor constructs utilizing antigen-binding moieties (e.g., generated from single-chain fragments (scFvs)) offer the added advantage of being "universal," in that they bind native antigens on target cell surfaces in an HLA-independent manner.

[0176] The CAR embodiments described herein include nucleic acids encoding antigen-specific CAR polypeptides comprising an intracellular signaling domain, a transmembrane domain, and an extracellular domain comprising an antigen-binding domain. CARs can recognize epitopes consisting of shared spaces between one or more antigens. Optionally, CARs can include a hinge domain located between the transmembrane domain and the antigen-binding domain. CARs can further include a signal peptide that directs CAR expression to the cell surface. For example, CARs can include a signal peptide from GM-CSF. CARs can also be co-expressed with membrane-bound cytokines to improve persistence. For example, CARs can be co-expressed with membrane-bound IL-15.

[0177] Depending on the arrangement of the CAR domains and the particular sequences used in the domains, immune effector cells expressing the CAR can have different levels of activity against target cells. Different CAR sequences are introduced into immune effector cells to generate engineered cells, which can be selected for elevated SRCs, and the selected cells can be tested for activity to identify CAR constructs predicted to have the greatest therapeutic efficacy.

[0178] Chimeric antigen receptors can be produced by any means known in the art, but are preferably produced using recombinant DNA techniques. Nucleic acid sequences encoding several regions of chimeric antigen receptors can be prepared and assembled into complete coding sequences using standard molecular cloning techniques (genomic library screening, PCR, primer-assisted ligation, scFv libraries from yeast and bacteria, site-directed mutagenesis, etc.). The resulting coding regions can be inserted into expression vectors and used to transform suitable expression host allogeneic or autoimmune effector cells, such as T cells or NK cells.

[0179] The chimeric construct can be introduced into immune effector cells as naked DNA or in a suitable vector. Methods for stably transfecting cells by electroporation using naked DNA are known in the art. See, for example, U.S. Patent No. 6,410,319. Naked DNA generally refers to the DNA encoding the chimeric receptor contained in a plasmid expression vector in the appropriate direction for expression. Alternatively, a viral vector (e.g., a retroviral vector, an adenoviral vector, an adeno-associated viral vector, or a lentiviral vector) can be used to introduce the chimeric construct into immune effector cells. The vector suitable for use in the method of the present invention is non-replicative in immune effector cells. Many virus-based vectors are known, and the copy number of the virus maintained in cells is low enough to maintain cell viability, such as, for example, vectors based on HIV, SV40, EBV, HSV, or BPV.

[0180] A. Antigen-binding domain The antigen-binding domain may comprise the complementarity-determining region of a monoclonal antibody, the variable region of a monoclonal antibody, and / or an antigen-binding fragment thereof. The antigen-binding region or domain may comprise the VH and VL chain fragments of a single-chain variable fragment (scFv) derived from a particular mouse, human, or humanized monoclonal antibody. The fragment may also be any number of different antigen-binding domains of an antigen-specific antibody. The fragment may be an antigen-specific scFv encoded by a sequence optimized for human codon usage in expression in human cells. In certain embodiments, the VH and VL domains of the CAR are separated by a linker sequence, such as a Whitlow linker.

[0181] A prototype CAR encodes an scFv comprising VH and VL domains from a single monoclonal antibody (mAb) linked to a transmembrane domain and one or more cytoplasmic signaling domains (e.g., a costimulatory domain and a signaling domain). Thus, the CAR may comprise the LCDR1-3 and HCDR1-3 sequences of an antibody that binds to B7-H3. However, in further embodiments, two of many antibodies that bind to an antigen of interest are identified, and a CAR is constructed comprising (1) the HCDR1-3 sequence of the first antibody that binds to the antigen, and (2) the LCDR1-3 sequence of the second antibody that binds to the antigen. Such a CAR, comprising HCDR and LCDR sequences from two different antigen-binding antibodies, may have the advantage of preferentially binding to a particular conformation of the antigen (e.g., a conformation preferentially associated with cancer cells relative to normal tissues).

[0182] Alternatively, CARs can be engineered using VH and VL chains from different mAbs to generate a panel of CAR+ immune effector cells. The antigen-binding domain of the CAR can comprise any combination of the LCDR1-3 sequences of a first antibody and the HCDR1-3 sequences of a second antibody.

[0183] B. Hinge domain The CAR polypeptide may include a hinge domain located between the antigen-binding domain and the transmembrane domain. In some instances, the hinge domain is included in the CAR polypeptide to provide sufficient distance between the antigen-binding domain and the cell surface, or to alleviate the possibility of steric hindrance that may adversely affect antigen binding or the effector function of the CAR-modified immune effector cell. The hinge domain may include a sequence that binds to an Fc receptor, such as FcγR2a or FcγR1a. For example, the hinge sequence may include an Fc domain from a human immunoglobulin (e.g., IgG1, IgG2, IgG3, IgG4, IgA1, IgA2, IgM, IgD, or IgE) that binds to an Fc receptor.

[0184] The CAR hinge domain can be derived from a human immunoglobulin (Ig) constant region or a portion thereof including an Ig hinge, or can be derived from a human CD8α transmembrane domain and CD8a-hinge region. The CAR hinge domain can include the hinge-CH2-CH3 region of an antibody isotype IgG4. The hinge domain (and / or CAR) may not include the wild-type human IgG4 CH2 and CH3 sequences. Point mutations can be introduced into the antibody heavy chain CH2 domain to reduce glycosylation and nonspecific Fcγ receptor binding of CAR-modified immune effector cells.

[0185] The CAR hinge domain may comprise an Ig Fc domain containing at least one mutation that reduces Fc-receptor binding compared to a wild-type Ig Fc domain. For example, the CAR hinge domain may comprise an IgG4-Fc domain containing at least one mutation that reduces Fc-receptor binding compared to a wild-type IgG4-Fc domain. The CAR hinge domain may comprise an IgG4-Fc domain having a mutation (such as an amino acid deletion or substitution) at a position corresponding to L235 and / or N297 relative to the wild-type IgG4-Fc sequence. For example, the CAR hinge domain may comprise an IgG4-Fc domain having an L235E and / or N297Q mutation relative to the wild-type IgG4-Fc sequence. The CAR hinge domain may comprise an IgG4-Fc domain having an amino acid substitution at position L235 with an amino acid that is hydrophilic, such as R, H, K, D, E, S, T, N, or Q, or has properties similar to "E," such as D. The CAR hinge domain may comprise an IgG4-Fc domain with an amino acid substitution at position N297 with an amino acid with properties similar to "Q", such as S or T.

[0186] The hinge domain may comprise a sequence that is about 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to an IgG4 hinge domain, a CD8a hinge domain, a CD28 hinge domain, or an engineered hinge domain.

[0187] C. Transmembrane domain The antigen-specific extracellular domain and the intracellular signaling domain can be connected by a transmembrane domain.Polypeptide sequences that can be used as part of the transmembrane domain include, but are not limited to, human CD4 transmembrane domain, human CD28 transmembrane domain, transmembrane human CD3 zeta domain, cysteine-mutated human CD3 zeta domain, or other transmembrane domains from other human transmembrane signaling proteins such as CD16, CD8, and erythropoietin receptor.For example, the transmembrane domain can include a sequence that is at least 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% identical to one of the sequences provided in U.S. Patent Publication No. 2014 / 0274909 (e.g., CD8 and / or CD28 transmembrane domain) or U.S. Patent No. 8,906,682 (e.g., CD8α transmembrane domain), both of which are incorporated herein by reference. The transmembrane region can be derived from (i.e., comprise at least the transmembrane region of) the alpha, beta, or zeta chain of the T cell receptor, CD3 epsilon, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137, CD154. In certain embodiments, the transmembrane domain can be 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to the CD8a transmembrane domain or the CD28 transmembrane domain.

[0188] D. Intracellular signaling domains The intracellular signaling domain of a CAR is responsible for activating at least one of the normal effector functions of immune cells engineered to express the CAR. The term "effector function" refers to the specialized function of a differentiated cell. The effector function of a T cell can be, for example, cytolytic activity or helper activity, including cytokine secretion. The effector function of naive, memory, or memory T cells includes antigen-dependent proliferation. Thus, the term "intracellular signaling domain" refers to the portion of a protein that transmits an effector function signal and induces the cell to perform a specialized function. The intracellular signaling domain can be derived from the intracellular signaling domain of a native receptor. Examples of such native receptors include the zeta chain of the T cell receptor, or any of its homologs (e.g., eta, delta, gamma, or epsilon), MB1 chain, B29, Fc RIII, Fc RI, and combinations of signaling molecules such as CD3ζ and CD28, CD27, 4-1BB / CD137, ICOS / CD278, IL-2Rβ / CD122, IL-2Rα / CD132, DAP10, DAP12, CD40, OX40 / CD134, and combinations thereof, as well as other similar molecules and fragments. Intracellular signaling portions of other members of the family of activating proteins can be used.

[0189] Although the entire intracellular signaling domain can be used, it is often not necessary to use the entire intracellular polypeptide. To the extent that a truncated portion of the intracellular signaling domain is available, such a truncated portion can be used instead of the intact chain, as long as it still transmits an effector function signal. Thus, the term "intracellular signaling domain" refers to a truncated portion of the intracellular signaling domain sufficient to transmit an effector function signal when the CAR binds to a target. One or more cytoplasmic domains can be used as so-called third-generation CARs, having at least two or three signaling domains fused together for additive or synergistic effects; for example, CD28 and 4-1BB can be combined in a CAR construct. In certain embodiments, the intracellular signaling domain comprises a sequence that is 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to a domain comprising a CD3ζ intracellular domain, a CD28 intracellular domain, a CD137 intracellular domain, or a CD28 intracellular domain fused to a 4-1BB intracellular domain.

[0190] E. Immune effector cells Immune effector cells can be T cells (e.g., regulatory T cells, CD4+ T cells, CD8+ T cells, or gamma-delta T cells), natural killer (NK) cells, invariant NK cells, or NKT cells. Also provided herein are methods for producing and manipulating immune effector cells, as well as methods for using and administering cells for adoptive cell therapy, where cells can be autologous or allogeneic. Thus, immune effector cells can be used as immunotherapy, for example, to target cancer cells.

[0191] Immune effector cells can be isolated from a subject, particularly a human subject.Immune effector cells can be obtained from a subject of interest, such as a subject suspected of having a certain disease or condition, a subject suspected of having a predisposition to a certain disease or condition, a subject undergoing therapy for a certain disease or condition, a healthy volunteer or a healthy donor, or from a blood bank.Immune effector cells can be collected, enriched, and / or purified from any tissue or organ that exists in a subject, including but not limited to blood, umbilical cord blood, spleen, thymus, lymph node, bone marrow, tissue removed and / or exposed during surgical procedure, and tissue obtained through biopsy procedure.Isolated immune effector cells can be used directly or can be stored for a certain period of time, such as by freezing.

[0192] The tissues / organs from which immune effector cells are enriched, isolated, and / or purified can be isolated from both living and non-living subjects, and non-living subjects are organ donors.Immune effector cells isolated from umbilical cord blood can have enhanced immunoregulatory ability, as measured by CD4 or CD8 positive T cell suppression.Immune effector cells can be isolated from pooled blood, particularly pooled umbilical cord blood, for enhanced immunoregulatory ability.Pooled blood can be from two or more sources, such as 3, 4, 5, 6, 7, 8, 9, 10 or more sources (e.g., donor subjects).

[0193] The immune cell population can be obtained from the subject who needs therapy or the subject who suffers from the disease related to the decrease of immune effector cell activity.Therefore, the cells are autologous to the subject who needs therapy.Alternatively, the immune effector cell population can be obtained from a donor, preferably an allogeneic donor.Allogeneic donor cells can be human leukocyte antigen (HLA) compatible or not.To make them compatible with the subject, allogeneic cells can be treated to reduce immunogenicity.

[0194] 1.T cells The immune effector cells can be T cells. The T cells can be derived from blood, bone marrow, lymph, umbilical cord, or lymphoid organs. The T cells can be human T cells. The T cells are typically primary cells, such as cells isolated directly from a subject and / or isolated and frozen from a subject. The cells can be selected from the total T cell population, CD4 T cells, CD4+ ... + cells, CD8 + The cells may include one or more subsets of T cells or other cell types, such as cells and their subpopulations.With respect to the subject to be treated, the cells may be allogeneic and / or autologous.In off-the-shelf technology, the cells may be derived from multipotent and / or pluripotent cells, such as stem cells, such as induced pluripotent stem cells (iPSCs).

[0195] T cell subtypes and subpopulations (e.g., CD4 + and / or CD8 + Among T cells, naive T (T N ) cells, effector T cells (T EFF ), memory T cells, and their subtypes, such as stem cell memory T (TSC M ), Central Memory T(TC M ), Effector Memory T(T EM ), or terminally differentiated effector memory T cells, tumor-infiltrating lymphocytes (TILs), immature T cells, mature T cells, helper T cells, cytotoxic T cells, mucosal-associated invariant T (MAIT) cells, natural and adaptive regulatory T (Treg) cells, helper T cells, such as TH1 cells, TH2 cells, TH3 cells, TH17 cells, TH9 cells, TH22 cells, follicular helper T cells, alpha / beta T cells, and delta / gamma T cells.

[0196] One or more of the T cell populations may be enriched or depleted for cells that are positive for a particular marker, such as a surface marker, or negative for a particular marker. In some examples, such markers are absent or expressed at relatively low levels in certain T cell populations (e.g., non-memory cells) but present or expressed at relatively high levels in certain other T cell populations (e.g., memory cells).

[0197] T cells can be isolated from PBMC samples by negative selection for markers expressed on non-T cells, such as B cells, monocytes, or other white blood cells, such as CD14. In some embodiments, CD4 + or CD8 + Using a selection stage, CD4 + Helper and CD8 + Isolate cytotoxic T cells. + and CD8 + The population can be further sorted into subpopulations by positive or negative selection for markers that are expressed or expressed to a relatively high degree in one or more naive, memory, and / or effector T cell subpopulations.

[0198] CD8 + T cells can be further enriched or depleted into naive, central memory, effector memory, and / or central memory stem cells, such as by positive or negative selection based on the surface antigens associated with each subpopulation. CM ) Cell enrichment can be performed to increase efficacy, such as improving long-term survival, expansion, and / or engraftment after administration, and in some embodiments is particularly robust in such subpopulations.

[0199] The T cells can be autologous T cells. In this method, a tumor sample is obtained from the patient to obtain a single cell suspension. The single cell suspension can be obtained by any suitable means, for example, mechanically (e.g., disaggregating the tumor using a gentleMACS™ Dissociator, Miltenyi Biotec, Auburn, Calif.) or enzymatically (e.g., collagenase or DNase). A single cell suspension of the tumor enzymatic digest is cultured in interleukin-2 (IL-2). Cells are grown to confluency (e.g., approximately 2×10 6 The cells are cultured for, for example, about 5 to about 21 days, preferably about 10 to about 14 days, until the number of lymphocytes reaches 10 ...

[0200] Cultured T cells can be pooled and rapidly expanded. Rapid expansion provides at least about a 50-fold (e.g., 50-fold, 60-fold, 70-fold, 80-fold, 90-fold, or 100-fold or more) increase in the number of antigen-specific T cells over a period of about 10 to about 14 days. More preferably, rapid expansion provides at least about a 200-fold (e.g., 200-fold, 300-fold, 400-fold, 500-fold, 600-fold, 700-fold, 800-fold, 900-fold or more) increase in the number of antigen-specific T cells over a period of about 10 to about 14 days.

[0201] Expansion can be achieved by any of several methods known in the art. For example, T cells can be rapidly expanded using nonspecific T cell receptor stimulation in the presence of feeder lymphocytes and either interleukin-2 (IL-2) or interleukin-15 (IL-15), preferably with the addition of IL-2. Nonspecific T cell receptor stimulation can include approximately 30 ng / ml of OKT3, a mouse monoclonal anti-CD3 antibody (available from Ortho-McNeil®, Raritan, NJ). Alternatively, T cells can be rapidly expanded by in vitro stimulation of peripheral blood mononuclear cells (PBMCs) with one or more antigens of cancer (including antigenic portions thereof, such as epitopes, or cells), optionally expressed from a vector, such as a human leukocyte antigen A2 (HLA-A2)-binding peptide, in the presence of a T cell growth factor, such as 300 IU / ml of IL-2 or IL-15, preferably with the addition of IL-2. In vitro-induced T cells are rapidly expanded by restimulating HLA-A2-expressing antigen-presenting cells with the same antigen of the cancer that was pulsed. Alternatively, T cells can be restimulated with, for example, irradiated autologous lymphocytes or irradiated HLA-A2+ allogeneic lymphocytes and IL-2.

[0202] Autologous T cells can be modified to express T cell growth factors that promote the proliferation and activation of autologous T cells. Suitable T cell growth factors include, for example, interleukin (IL)-2, IL-7, IL-15, and IL-12. Suitable modification methods are known in the art. See, for example, Sambrook et al., MOLECULAR CLONING: A LABORATORY MANUAL, 3 rded., Cold Spring Harbor Press, Cold Spring Harbor, NY 2001 and Ausubel et al., CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, Greene Publishing Associates and John Wiley & Sons, NY, 1994. In certain embodiments, the modified autologous T cells express high levels of T cell growth factors. T cell growth factor coding sequences, such as those of IL-12, are readily available in the art, as are promoters, the operably linking of which to the T cell growth factor coding sequence promotes high levels of expression.

[0203] 2.NK cells Immune effector cells can be natural killer (NK) cells. Natural killer (NK) cells are a subpopulation of lymphocytes with natural cytotoxicity against various tumor cells, virus-infected cells, and some normal cells in the bone marrow and thymus. NK cells are important effectors of the early innate immune response against transformed and virus-infected cells. NK cells comprise approximately 10% of lymphocytes in human peripheral blood. When lymphocytes are cultured in the presence of interleukin 2 (IL-2), a strong cytotoxic response develops. NK cells are effector cells known as large granular lymphocytes due to their large size and the presence of characteristic azurophilic granules in their cytoplasm. NK cells differentiate and mature in the bone marrow, lymph nodes, spleen, tonsils, and thymus. NK cells can be detected in humans by specific surface markers, such as CD16, CD56, and CD8. NK cells do not express T cell antigen receptors, the pan-T marker CD3, or surface immunoglobulin B cell receptors.

[0204] NK cell stimulation is achieved through the crosstalk of signals derived from cell surface activating and inhibitory receptors. The activation state of NK cells is regulated by the balance of intracellular signals received from numerous germline-encoded activating and inhibitory receptors. When NK cells encounter abnormal cells (e.g., tumor cells or virus-infected cells) and activating signals prevail, NK cells can rapidly induce apoptosis of the target cell through the directed secretion of perforin-containing cytolytic granules and granzymes or through the binding of death domain-containing receptors. Activated NK cells can also secrete type I cytokines, such as interferon-γ, tumor necrosis factor-α, and granulocyte-macrophage colony-stimulating factor (GM-CSF), which activate both innate and adaptive immune cells as well as other cytokines. The production of these soluble factors by NK cells during the early innate immune response significantly influences the recruitment and function of other hematopoietic cells. Through physical contact and cytokine production, NK cells also play a central role in a regulatory crosstalk network with dendritic cells and neutrophils to promote or suppress immune responses.

[0205] NK cells can be derived from human peripheral blood mononuclear cells (PBMCs), unstimulated leukapheresis products (PBSCs), human embryonic stem cells (hESCs), induced pluripotent stem cells (iPSCs), bone marrow, or umbilical cord blood by methods well known in the art. In certain embodiments, NK cells are isolated and expanded ex vivo. For example, CB mononuclear cells can be isolated by Ficoll density gradient centrifugation and cultured in a bioreactor with IL-2 and artificial antigen-presenting cells (aAPCs). After 7 days, the cell culture can be depleted of any cells expressing CD3 and re-cultured for another 7 days. The cells can be again depleted for CD3 and CD56 expression. + / CD3 - In another method, umbilical cord CB can be used to characterize the CD34 + Isolation of CD56 cells by culturing them in medium containing SCF, IL-7, IL-15, and IL-2+ / CD3 - Differentiation into cells can lead to NK cells.

[0206] F. Manipulation of Immune Effector Cells Immune effector cells (e.g., autologous or allogeneic T cells (e.g., regulatory T cells, CD4+ T cells, CD8+ T cells, or gamma-delta T cells), NK cells, invariant NK cells, or NKT cells) can be genetically engineered to express an antigen receptor, such as a chimeric antigen receptor (CAR). For example, host cells (e.g., autologous or allogeneic T cells) can be modified to express a CAR with antigen specificity for B7-H3. In certain embodiments, NK cells are engineered to express a CAR. Multiple CARs, such as those directed against different antigens, can be added to a single cell type, such as a T cell or an NK cell.

[0207] The cells may contain one or more nucleic acids introduced via genetic engineering that encode one or more antigen receptors, as well as the genetically engineered products of such nucleic acids. The nucleic acids may be heterologous, i.e., not normally present in the cell or sample obtained from the cell, such as those obtained from another organism or cell not normally found in the genetically engineered cell and / or the organism from which the cell is derived. The nucleic acids may not be naturally occurring, such as nucleic acids not found in nature (e.g., chimeras).

[0208] IV. Pharmaceutical Preparations The present disclosure provides pharmaceutical compositions comprising an antibody that selectively targets B7-H3. Such compositions comprise a prophylactically or therapeutically effective amount of the antibody or a fragment thereof and a pharmaceutically acceptable carrier. Also provided herein are pharmaceutical compositions and formulations comprising immune cells (e.g., T cells or NK cells) expressing a CAR and a pharmaceutically acceptable carrier.

[0209] The phrases "pharmaceutically or pharmacologically acceptable" refer to molecular entities and compositions that do not produce adverse, allergic, or other untoward reactions when administered to an animal, such as a human, as appropriate. The preparation of pharmaceutical compositions containing an antibody or additional active ingredient will be known to those of skill in the art in light of the present disclosure. Moreover, it will be understood that for animal (e.g., human) administration, preparations should meet sterility, pyrogenicity, general safety, and purity standards as required by the FDA Office of Biological Standards.

[0210] As used herein, "pharmaceutically acceptable carriers" include any aqueous solvents (e.g., water, alcoholic / aqueous solutions, saline, parenteral vehicles such as sodium chloride, Ringer's dextrose, etc.), non-aqueous solvents (e.g., propylene glycol, polyethylene glycol, vegetable oils, and injectable organic esters such as ethyl oleate), dispersion media, coatings, surfactants, antioxidants, preservatives (e.g., antibacterial or antifungal agents, antioxidants, chelating agents, and inert gases), isotonic agents, absorption delaying agents, salts, drugs, drug stabilizers, gels, binders, excipients, disintegrants, lubricants, sweeteners, flavoring agents, dyes, fluid and nutrient supplements, such similar materials and combinations thereof, which will be known to those skilled in the art. The pH and exact concentration of the various components in a pharmaceutical composition are adjusted according to well-known parameters.

[0211] The active ingredient can be formulated for parenteral administration, for example, for injection via intravenous, intramuscular, intratumoral, subcutaneous, or even intraperitoneal routes. Typically, such compositions can be prepared as either liquid solutions or suspensions, and solid forms suitable for use in preparing solutions or suspensions by addition of liquid prior to injection can also be prepared, and the preparations can also be emulsified.

[0212] The therapeutic compositions of the present embodiments are advantageously administered in the form of injectable compositions, either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid prior to injection can also be prepared. These preparations can also be emulsified.

[0213] Pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions, formulations including sesame oil, peanut oil, or aqueous propylene glycol, and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases, the form must be sterile and fluid to the extent that easy syringability exists. It must also be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi.

[0214] Proteinaceous compositions can be formulated in neutral or salt form.Pharmaceutically acceptable salts include acid addition salts (formed with free amino groups of protein), for example, with inorganic acids such as hydrochloric acid or phosphoric acid, or organic acids such as acetic acid, oxalic acid, tartaric acid, mandelic acid, etc.Salts formed with free carboxyl groups can also be derived from inorganic bases such as sodium, potassium, ammonium, calcium, or ferric hydroxide, and organic bases such as isopropylamine, trimethylamine, histidine, procaine, etc.

[0215] Pharmaceutical compositions can contain solvents or dispersion media containing, for example, water, ethanol, polyols (e.g., glycerol, propylene glycol, and liquid polyethylene glycol, etc.), suitable mixtures thereof, and vegetable oils. Proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by maintaining the required particle size in the case of dispersion, and by the use of surfactants. Prevention of microbial action can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it is preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of injectable compositions can be achieved by using agents that delay absorption, for example, aluminum monostearate and gelatin, in the composition.

[0216] If desired, the compositions can also contain minor amounts of wetting or emulsifying agents, or pH buffering agents. These compositions can take the form of solutions, suspensions, emulsions, tablets, pills, capsules, powders, sustained-release formulations, and the like. Oral formulations can include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharin, cellulose, magnesium carbonate, and the like. Examples of suitable pharmaceuticals are described in Remington's Pharmaceutical Sciences. Such compositions contain a prophylactically or therapeutically effective amount of the antibody or fragment thereof, preferably in purified form, together with a suitable amount of carrier so as to provide the form for proper administration to the patient.

[0217] Passive transfer of antibodies generally involves the use of intravenous or intramuscular injections. The antibody form can be monoclonal. Such immunity is generally short-lived and carries the potential risk of hypersensitivity reactions and serum sickness, particularly from gamma globulins of non-human origin. The antibody is formulated in a carrier suitable for injection, i.e., sterile and injectable.

[0218] Generally, the components of the compositions of the present disclosure are supplied separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water-free concentrate in a sealed container such as an ampoule or sachet indicating the quantity of active agent. When the composition is administered by infusion, it can be dispensed in an infusion bottle containing sterile pharmaceutical-grade water or saline. When the composition is administered by injection, an ampoule of sterile water for injection or saline is provided, allowing the components to be mixed prior to administration.

[0219] In certain embodiments, pharmaceutical compositions may contain, for example, at least about 0.1% of the active ingredient. In other embodiments, the active ingredient may comprise between about 2% to about 75% of the weight of the unit, or between about 25% to about 60%, for example, and any range derivable therein.

[0220] The term "unit dose" or "dosage" refers to a physically discrete unit suitable for use in a subject, each unit containing a predetermined amount of a therapeutic composition calculated to produce the desired response, as described above, in conjunction with its administration, i.e., the appropriate route and treatment regimen. The amount administered depends on the desired effect, depending both on the number of treatments and the unit dose. The actual dosage of the compositions of the present embodiments administered to a patient or subject can be determined by physical and physiological factors, such as the subject's weight, age, health, and sex, the type of disease being treated, the degree of disease penetration, prior or concurrent therapeutic interventions, the patient's idiopathic disease, the route of administration, and the efficacy, stability, and toxicity of the particular therapeutic agent. For example, dosages can range from about 1 μg / kg / body weight to about 1000 mg / kg / body weight per administration (including any intermediate doses), or any range derivable therein. Non-limiting examples of ranges that may be derived from the values ​​recited herein include ranges of about 5 μg / kg / body weight to about 100 mg / kg / body weight, about 5 μg / kg / body weight to about 500 mg / kg / body weight, etc. The practitioner responsible for administration will, in any event, determine the concentration of active ingredient(s) in a composition and appropriate dose in the individual subject.

[0221] V. Treatment method Certain aspects of this embodiment can be used to prevent or treat diseases or disorders associated with elevated levels of B7-H3, such as renal, pancreatic, colorectal, non-small cell lung, ovarian, bladder, melanoma, prostate, and neuroectodermal cancers. B7-H3 function can be reduced by any suitable drug. Preferably, such a substance is an anti-B7-H3 antibody, an anti-B7-H3 antibody-drug conjugate, B7-H3-specific CAR T cells, or B7-H3-specific CAR NK cells.

[0222] "Treatment" and "treating" refer to the administration or application of a therapeutic agent to a subject, or the performance of a procedure or modality on a subject, for the purpose of obtaining a therapeutic benefit for a disease or health-related condition. For example, treatment can include the administration of a pharmaceutically effective amount of an antibody targeting B7-H3, either alone or in combination with the administration of chemotherapy, immunotherapy, or radiation therapy, surgery, or any combination thereof.

[0223] The term " subject " as used herein refers to any individual or patient that the method of interest is carried out.Generally, subject is human, but as those skilled in the art will understand, subject can also be animal.Therefore, other animals, including mammals such as rodents (including mice, rats, hamsters and guinea pigs), cats, dogs, rabbits, livestock (including cows, horses, goats, sheep, pigs, etc.), and primates (including monkeys, chimpanzees, orangutans and gorillas), are included in the definition of subject.

[0224] The term "therapeutic benefit" or "therapeutically effective" as used throughout this application refers to anything that promotes or enhances the health of a subject with respect to the medical treatment of the condition. This includes, but is not limited to, reducing the frequency or severity of signs or symptoms of the disease. For example, treating cancer can include, for example, reducing tumor size, reducing tumor invasiveness, reducing the rate of cancer growth, or preventing metastasis. Treating cancer can also refer to extending the survival of a subject with cancer.

[0225] As used herein, the term "cancer" can be used to describe a solid tumor, a metastatic cancer, or a non-metastatic cancer. In certain embodiments, the cancer can originate in the bladder, blood, bone, bone marrow, brain, breast, colon, esophagus, duodenum, small intestine, large intestine, colon, rectum, anus, gums, head, kidney, liver, lung, nasopharynx, cervix, ovary, pancreas, prostate, skin, stomach, testicles, tongue, or uterus.

[0226] Cancers, specifically, include the following histological types: neoplasm, malignant; carcinoma; carcinoma, undifferentiated; giant and spindle cell carcinoma; small cell carcinoma; papillary carcinoma; squamous cell carcinoma; lymphoepithelial carcinoma; basal cell carcinoma; ciliary body carcinoma; transitional cell carcinoma; papillary transitional cell carcinoma; adenocarcinoma; gastrinoma, malignant; cholangiocarcinoma; hepatocellular carcinoma; combined hepatocellular carcinoma and cholangiocarcinoma; trabecular adenocarcinoma; adenoid cystic carcinoma; adenocarcinoma of adenomatous polyps; adenocarcinoma, familial adenomatous polyposis; solid tumor; carcinoid tumor, malignant; branchial-gingival adenocarcinoma; papillary adenocarcinoma; chromophobe carcinoma; eosinophilic carcinoma; eosinophilic adenocarcinoma; basophilic carcinoma; clear cell Adenocarcinoma;Granular cell carcinoma;Follicular adenocarcinoma;Papillary and follicular adenocarcinoma;Non-encapsulated sclerosing carcinoma;Adrenal cortical carcinoma;Endometrial carcinoma;Cutaneous adenocarcinoma;Apocrine adenocarcinoma;Sebaceous gland carcinoma;Cervical adenocarcinoma;Mucous epidermoid carcinoma;Cystadenocarcinoma;Papillary cystadenocarcinoma;Papillary serous cystadenocarcinoma;Mucinous cystadenocarcinoma;Mucinous adenocarcinoma;Signet ring cell carcinoma;Invasive ductal carcinoma;Medullary carcinoma;Lobular carcinoma;Inflammatory carcinoma;Paget's disease of the breast;Adenocyte carcinoma;Adenosquamous carcinoma;Adenocarcinoma with squamous metaplasia;Thymoma, malignant;Ovarian stromal tumor, malignant;Capsular, malignant;Granulosa cell tumor, malignant;Androblastoma, malignant; Sertoli cell carcinoma; Leydig cell tumor, malignant; Lipid cell tumor, malignant; Paraganglioma, malignant; Extramammary paraganglioma, malignant; Pheochromocytoma; Hemangiosarcoma; Malignant melanoma; Amelanotic melanoma; Superficial melanoma; Malignant melanoma in giant pigmented nevus; Epithelioid cell melanoma; Blue nevus, malignant; Sarcoma; Fibrosarcoma; Fibrous histiocytoma, malignant; Myxosarcoma; Liposarcoma; Leiomyosarcoma; Rhabdomyosarcoma; Embryonic rhabdomyosarcoma; Alveolar rhabdomyosarcoma; Stromal sarcoma; Mixed tumor, malignant; Müllerian mixed tumor; Nephroblastoma; Hepatoblastoma; Carcinosarcoma; Mesenchymoma, malignant; Brenner tumor, malignant; Phyllodes tumor, malignant; Synovial sarcoma; Interstitial Dysgerminoma, malignant; Dysgerminoma; Embryonic carcinoma; Teratoma, malignant; Ovarian goiter, malignant; Choriocarcinoma; Mesonephroma, malignant; Angiosarcoma; Hemangioendothelioma, malignant; Kaposi's sarcoma; Hemangiopericytoma, malignant; Lymphangiosarcoma; Osteosarcoma; Paracortical osteosarcoma; Chondrosarcoma; Chondroblastoma, malignant; Mesenchymal chondrosarcoma; Giant cell tumor of bone; Ewing's sarcoma; Odontogenic tumor, malignant; Ameloblastic odontosarcoma; Ameloblastoma, malignant; Ameloblastic fibrosarcoma; Pineal tumor, malignant; Chordoma; Glioma, malignant; Ependymoma; Astrocytoma; Protoplasmic astrocytoma; Fibrillar astrocytoma; Astroblastoma; Glioblastoma; Oligodendroglioma;Oligodendroglioma;Primitive neuroectodermal;Cerebellar sarcoma;Ganglioneuroblastoma;Neuroblastoma;Retinoblastoma;Olfactory neurogenic tumor;Meningioma, malignant;Neurofibrosarcoma;Neurilemoma, malignant;Granular cell tumor, malignant;Malignant lymphoma;Hodgkin's disease;Hodgkin's lymphoma;Paragranuloma;Malignant lymphoma, small lymphocytic;Malignant lymphoma, large cell, diffuse;Malignant lymphoma, follicular;Mycosis fungoides;Other The present invention may be used to treat, but is not limited to, certain non-Hodgkin's lymphomas, malignant histiocytosis, multiple myeloma, mast cell sarcoma, immunoproliferative small intestinal disease, leukemia, lymphocytic leukemia, plasma cell leukemia, erythroleukemia, lymphosarcoma cell leukemia, myeloid leukemia, basophilic leukemia, eosinophilic leukemia, monocytic leukemia, mast cell leukemia, megakaryoblastic leukemia, myeloid sarcoma, and hairy cell leukemia. Nevertheless, it is recognized that the present invention may also be used to treat non-cancerous diseases (e.g., fungal infections, bacterial infections, viral infections, neurodegenerative diseases, and / or genetic disorders).

[0227] In certain embodiments, the compositions and methods of this embodiment comprise an antibody or antibody fragment against B7-H3 in combination with a second or additional therapy, such as chemotherapy or immunotherapy. Such therapy can be applied to the treatment of any disease associated with elevated B7-H3. For example, the disease can be cancer.

[0228] Methods and compositions involving combination therapy enhance the therapeutic or protective effect and / or increase the therapeutic efficacy of another anti-cancer or anti-hyperproliferative therapy. Therapeutic and prophylactic methods and compositions can be provided in combined amounts effective to achieve a desired effect, such as killing cancer cells and / or inhibiting cellular hyperproliferation. This process can include contacting cells with both an antibody or antibody fragment and a second therapy. Tissues, tumors, or cells can be contacted with one or more compositions or pharmacological formulations containing one or more agents (i.e., antibodies or antibody fragments or anti-cancer agents), or by contacting tissues, tumors, and / or cells with two or more different compositions or formulations, where one composition provides 1) an antibody or antibody fragment, 2) an anti-cancer agent, or 3) both an antibody or antibody fragment and an anti-cancer agent. It is also contemplated that such combination therapy can be used in conjunction with chemotherapy, radiation therapy, surgery, immunotherapy, or radioimmunotherapy.

[0229] The terms "contacted" and "exposed" when applied to a cell are used herein to describe the process by which a therapeutic construct and a chemotherapeutic or radiotherapeutic agent are delivered to or directly juxtaposed with a target cell. To achieve cell killing, for example, both agents are delivered to the cell in a combined amount effective to kill the cell or prevent it from dividing.

[0230] The antibody may be administered before, during, or after the anti-cancer therapy, or in various combinations. Administration may occur at intervals ranging from simultaneous administration to minutes, days, or weeks. In embodiments in which the antibody or antibody fragment is provided to the patient separately from the anti-cancer drug, it is generally best to ensure that there is no significant time between each delivery, allowing the two compounds to still exert their beneficially combined effect on the patient. In such instances, it is contemplated that the antibody therapy and anti-cancer therapy may be provided to the patient within about 12-24 or 72 hours of each other, more specifically within about 6-12 hours of each other. In some situations, where several days (2, 3, 4, 5, 6, or 7) to several weeks (1, 2, 3, 4, 5, 6, 7, or 8) elapse between each administration, significantly extending the treatment period may be desirable.

[0231] In certain embodiments, the course of treatment lasts from 1 to 90 days or more (such ranges are inclusive). It is contemplated that one agent may be given on any day from day 1 to day 90 (such ranges are inclusive), or any combination thereof, and another agent may be given on any day from day 1 to day 90 (such ranges are inclusive), or any combination thereof. Within a single day (24-hour period), a patient may receive one or more doses of an agent. It is further contemplated that, following the course of treatment, there will be a period during which no anti-cancer drug therapy is administered. This period can last from 1 to 7 days, and / or from 1 to 5 weeks, and / or from 1 to 12 months or more (such ranges are inclusive), depending on the patient's prognosis, strength, health, and other conditions. It is anticipated that the treatment cycle will be repeated as necessary.

[0232] Various combinations can be used. In the example below, the antibody therapy is "A" and the anti-cancer therapy is "B". TIFF0007779484000001.tif17128

[0233] Administration of any compound or therapy of the present embodiments to a patient will follow general protocols for administration of such compounds, taking into account the toxicity, if any, of the agent. Thus, in some embodiments, there is a step of monitoring for toxicity resulting from the combination therapy.

[0234] A. Chemotherapy A wide variety of chemotherapeutic agents can be used in accordance with this embodiment. The term "chemotherapy" refers to the use of drugs to treat cancer. "Chemotherapeutic agent" is used to refer to a compound or composition administered to treat cancer. These agents or drugs are classified by their mode of activity within cells, such as whether and at what stage they affect the cell cycle. Alternatively, agents can be characterized based on their ability to directly crosslink DNA, intercalate DNA, or induce chromosomal and mitotic abnormalities by affecting nucleic acid synthesis. Alternatively, agents can inhibit specific enzyme activity within cells, such as kinases, phosphatases, lipases, methyltransferases, ethyltransferases, and dioxygenases. Alternatively, agents can block hormone activity, inhibit signal transduction, alter gene expression, induce apoptosis, or inhibit angiogenesis. Alternatively, agents can include cancer vaccines or gene therapies.

[0235] Examples of chemotherapeutic agents include alkylating agents such as thiotepa and cyclosphosphamide; alkyl sulfonates such as busulfan, improsulfan, and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; ethylenimines and methylamelamines, including altretamine, triethylenemelamine, triethylenephosphoramide, triethylenethiophosphoramide, and trimethylolmelamine; acetogenins (particularly bullatacin and bullatacinone); camptothecins (including the synthetic analog topotecan); bryostatin; kallistatin; CC-1065 (including its adozelesin, carzelesin, and bizelesin synthetic analogs); cryptophycins (particularly cryptophycin 1 and cryptophycin 8); dolastatins; duocarmycins (synthetic analogs, including KW-2189 and CB1-TM1); eleutherobin; pancratistatin; sarkozyme; spongistatin; nitrogen mustards such as chlorambucil, chlornaphazine, colofosfamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine hydrochloride, melphalan, nobembine, fenesterine, prednimustine, trofosfamide, and uracil mustard; nitrosoureas such as carmustine, chlorozotocin, fotemustine, lomustine, nimustine, and ranimnustine; antibiotics such as enediyne antibiotics (e.g., calicheamicin, especially calicheamicin gamma 1I and calicheamicin omega 1I); dynemicins, including dynemicin A; bisphosphonates such as clodronate; esperamicin;Neocarzinostatin chromophore and related chromoprotein enediyne antibiotic chromophores, aclacinomycin, actinomycin, autarrhalicin, azaserine, bleomycin, cactinomycin, carabicin, carminomycin, carzinophilin, chromomycin, dactinomycin, daunorubicin, detorubicin, 6-diazo-5-oxo-L-norleucine, doxorubicin (including morpholino-doxorubicin, cyanomorpholino-doxorubicin, 2-pyrrolino-doxorubicin, and deoxydoxorubicin), epirubicin Mitomycins such as esorubicin, idarubicin, marcelomycin, mitomycin C, mycophenolic acid, nogalarmicin, olivomycin, peplomycin, potfilomycin, puromycin, keramicin, rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex, zinostatin, and zorubicin; antimetabolites such as methotrexate and 5-fluorouracil (5-FU); folic acid analogs such as denopterin, pteropterin, and trimetrexate; fludarabine, 6-mercaptopurine Purine analogues such as ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, doxifluridine, enocitabine, and floxuridine; androgens such as calucelone, drostanolone propionate, epitiostanol, mepitiostane, and testolactone; antiadrenal agents such as mitotane and trilostane; folic acid supplements such as furoic acid; aceglatone; aldophosphamide glycosides; aminolevulinic acid; eniluracyl; amsacrine; bess Trabucil; Bisantrene; Edatraxate; Defofamine; Demecolcine; Diaziquone; Elformitin; Elliptinium acetate; Epothilone; Etoglucide; Gallium nitrate; Hydroxyurea; Lentinan; Lonidynin; Maytansinoids such as maytansine and ansamitocin; Mitoguazone; Mitoxantrone; Mopidanmol; Nitraerin; Pentostatin; Fenamet; Pirarubicin; Rosoxantrone; Podophyllic acid; 2-ethylhydrazide; Procarbazine; PSK polysaccharide complex; Razoxane; Rhizoxin; Sizofiran;Spirogermanium; tenuazonic acid; triaziquone; 2,2',2''-trichlorotriethylamine; trichothecenes (especially T-2 toxin, veracrine A, roridin A, and anguidine); urethane; vindesine; dacarbazine; mannomustine; mitobronitol; mitolactol; pipobroman; gacytosine; arabinoside ("Ara-C"); cyclophosphamide; taxoids, e.g., paclitaxel and docetaxel; gemcitabine; 6-thioguanine; mercaptopurine; platinum coordination complexes, such as cisplatin, oxaliplatin, and carboplatin; vinblastine; platinum; etoposide (VP-16 ); ifosfamide; mitoxantrone; vincristine; vinorelbine; novantrone; teniposide; edatrexate; daunomycin; aminopterin; xeloda; ibandronic acid; irinotecan (e.g., CPT-11); topoisomerase inhibitor RFS2000; difluoromethyl methylproline (DMFO); retinoids such as retinoic acid; capecitabine; carboplatin, procarbazine, plicomycin, gemcitabine, navelbine, farnesyl protein tranferase inhibitors, transplatin, and pharmaceutically acceptable salts, acids, or derivatives of any of the above.

[0236] Alternatively, any of a variety of molecular targeted therapeutic agents may be used in accordance with this embodiment, including, but not limited to, tyrosine kinase inhibitors (TKIs), PARP1 / 2 inhibitors, angiogenesis inhibitors, hormone blockers, gene expression regulators, epigenetic modifiers, and signal transduction inhibitors.

[0237] B. Radiation therapy Other factors that cause DNA damage and have been widely used include gamma rays, X-rays, and / or what are commonly known as directed delivery of radioisotopes to tumor cells. Other forms of DNA damage, such as microwaves, proton beam irradiation (U.S. Patent Nos. 5,760,395 and 4,870,287), and ultraviolet radiation, are also contemplated. All of these factors most likely cause widespread damage to DNA, DNA precursors, DNA replication and repair, and chromosome assembly and maintenance. X-ray doses range from daily doses of 50–200 roentgens over prolonged periods (3–4 weeks) to single doses of 2000–6000 roentgens. Dose ranges for radioisotopes vary widely and depend on the half-life of the isotope, the strength and type of radiation emitted, and uptake by neoplastic cells.

[0238] C. Immunotherapy Those skilled in the art will understand that immunotherapy can be used in conjunction with or in combination with the methods of the embodiments. In the context of cancer treatment, immunotherapy generally relies on the use of immune effector cells and molecules to target and destroy cancer cells. Rituximab (RITUXAN®) is one such example. The immune effector can be, for example, an antibody specific to some marker on the surface of tumor cells. The antibody alone can function as the therapeutic effector or can recruit other cells to actually affect cell killing. The antibody can also be conjugated to a drug or toxin (such as a chemotherapeutic agent, a radionuclide, ricin A chain, cholera toxin, pertussis toxin, etc.) and function simply as a targeting agent. Alternatively, the effector can be a lymphocyte bearing a surface molecule that interacts either directly or indirectly with the tumor cell target. Various effector cells include cytotoxic T cells and NK cells.

[0239] In one aspect of immunotherapy, tumor cells must have some marker that is amenable to targeting, i.e., not present on the majority of other cells. Many tumor markers exist, any of which may be suitable for targeting in the context of this embodiment. Common tumor markers include CD20, carcinoembryonic antigen, tyrosinase (p97), gp68, TAG-72, HMFG, sialyl Lewis antigen, MucA, MucB, PLAP, laminin receptor, erbB, and p155. An alternative aspect of immunotherapy is to combine anti-cancer effects with immunostimulatory effects. Immune stimulatory molecules also exist, including IL-2, IL-4, IL-12, GM-CSF, gamma-IFN, chemokines such as MIP-1, MCP-1, IL-8, and growth factors such as FLT3 ligand.

[0240] Examples of immunotherapies currently under investigation or in use include immune adjuvants such as Mycobacterium bovis, Plasmodium falciparum, dinitrochlorobenzene, and aromatic compounds (U.S. Patent Nos. 5,801,005 and 5,739,169; Hui and Hashimoto, 1998; Christodoulides et al., 1998); cytokine therapy such as interferon α, β, and γ, IL-1, GM-CSF, and TNF (Bukowski et al., 1998; Davidson et al., 1998; Hellstrand et al., 1998); gene therapy such as TNF, IL-1, IL-2, and p53 (Qin et al., 1998; Austin-Ward and Antibodies that have been used include antibodies against tumor cells, such as anti-CD20, anti-ganglioside GM2, and anti-p185 (Villaseca, 1998; U.S. Patent Nos. 5,830,880 and 5,846,945), and monoclonal antibodies, such as anti-CD20, anti-ganglioside GM2, and anti-p185 (Hollander, 2012; Hanibuchi et al., 1998; U.S. Patent No. 5,824,311). Alternatively, blocking the "don't eat me" signal (CD24) on tumor cells represents another strategy [PMID: 31367043]. It is contemplated that one or more anti-cancer therapies may be used in conjunction with the antibody therapies described herein.

[0241] In some embodiments, the immunotherapy can be an immune checkpoint inhibitor. Immune checkpoints either increase or decrease signals (e.g., costimulatory molecules). Immune checkpoint proteins that can be targeted by immune checkpoint blockade include adenosine A2A receptor (A2AR), B7-H3 (also known as CD276), B and T lymphocyte attenuator (BTLA), CCL5, CD27, CD38, CD8A, CMKLR1, cytotoxic T lymphocyte-associated protein 4 (CTLA-4, also known as CD152), CXCL9, CXCR5, glucocorticoid-inducible tumor necrosis factor receptor-related protein (GITR), HLA-DRB1, ICOS (also known as CD278), HLA-DQA1, HLA-E, indoleamine 2,3-dioxygenase 1 (IDO1 These include killer immunoglobulin (KIR), lymphocyte-activation gene-3 (LAG-3, also known as CD223), Mer tyrosine kinase (MerTK), NKG7, OX40 (also known as CD134), programmed death 1 (PD-1), programmed death-ligand 1 (PD-L1, also known as CD274), PDCD1LG2, PSMB10, STAT1, T cell immunoreceptor with Ig and ITIM domains (TIGIT), T cell immunoglobulin domain and mucin domain 3 (TIM-3), and V domain Ig suppressor of T cell activation (VISTA, also known as C10orf54). In particular, immune checkpoint inhibitors target the PD-1 axis and / or CTLA-4.

[0242] The immune checkpoint inhibitor can be a drug such as a small molecule, a recombinant form of a ligand or receptor, or an antibody such as a human antibody (e.g., International Patent Publication No. 2015 / 016718; Pardoll, Nat Rev Cancer, 12(4):252-264, 2012, both of which are incorporated herein by reference). Known inhibitors of immune checkpoint proteins or analogs thereof can be used, and in particular, chimeric, humanized, or human forms of antibodies can be used. As will be appreciated by those skilled in the art, alternative and / or synonymous names can be used for specific antibodies referred to in this disclosure. Such alternative and / or synonymous names are interchangeable within the context of this disclosure. For example, lambrolizumab is also known by the alternative and synonymous names MK-3475 and pembrolizumab.

[0243] In some embodiments, the PD-1 binding antagonist is a molecule that inhibits the binding of PD-1 to its ligand-binding partner. In certain embodiments, the PD-1 ligand-binding partner is PD-L1 and / or PD-L2. In another embodiment, the PD-L1 binding antagonist is a molecule that inhibits the binding of PD-L1 to its binding partner. In certain embodiments, the PD-L1 binding partner is PD-1 and / or B7-1. In another embodiment, the PD-L2 binding antagonist is a molecule that inhibits the binding of PD-L2 to its binding partner. In certain embodiments, the PD-L2 binding partner is PD-1. The antagonist can be an antibody, antigen-binding fragment thereof, immunoadhesin, fusion protein, or oligopeptide. Exemplary antibodies are described in U.S. Patent Nos. 8,735,553, 8,354,509, and 8,008,449, all of which are incorporated herein by reference. Other PD-1 axis antagonists for use in the methods provided herein are known in the art, such as those described in U.S. Patent Application Publication Nos. 2014 / 0294898, 2014 / 022021, and 2011 / 0008369, all of which are incorporated herein by reference.

[0244] In some embodiments, the PD-1 binding antagonist is an anti-PD-1 antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody). In some embodiments, the anti-PD-1 antibody is selected from the group consisting of nivolumab, pembrolizumab, and CT-011. In some embodiments, the PD-1 binding antagonist is an immunoadhesin (e.g., an immunoadhesin comprising the extracellular portion or PD-1-binding portion of PD-L1 or PD-L2 fused to a constant region (e.g., an Fc region of an immunoglobulin sequence)). In some embodiments, the PD-1 binding antagonist is AMP-224. Nivolumab, also known as MDX-1106-04, MDX-1106, ONO-4538, BMS-936558, and OPDIVO®, is an anti-PD-1 antibody described in WO 2006 / 121168. Pembrolizumab, also known as MK-3475, Merck3475, lambrolizumab, KEYTRUDA®, and SCH-900475, is an anti-PD-1 antibody described in WO2009 / 114335. CT-011, also known as hBAT or hBAT-1, is an anti-PD-1 antibody described in WO2009 / 101611. AMP-224, also known as B7-DCIg, is a PD-L2-Fc fusion soluble receptor described in WO2010 / 027827 and WO2011 / 066342.

[0245] Another immune checkpoint protein that can be targeted in the methods provided herein is cytotoxic T lymphocyte-associated protein 4 (CTLA-4), also known as CD152. The complete cDNA sequence of human CTLA-4 has Genbank accession number L15006. CTLA-4 is found on the surface of T cells and acts as an "off" switch when bound to CD80 or CD86 on the surface of antigen-presenting cells. CTLA-4 is similar to the T cell costimulatory protein CD28; both molecules bind to CD80 and CD86, also known as B7-1 and B7-2, respectively, on antigen-presenting cells. CTLA-4 transmits inhibitory signals to T cells, while CD28 transmits stimulatory signals. Intracellular CTLA-4 is also found on regulatory T cells and may be important for their function. T cell activation via the T cell receptor and CD28 results in increased expression of CTLA-4, an inhibitory receptor for the B7 molecule.

[0246] In some embodiments, the immune checkpoint inhibitor is an anti-CTLA-4 antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide.An anti-human CTLA-4 antibody (or a VH and / or VL domain derived therefrom) suitable for use in the present method can be generated using methods well known in the art.Alternatively, art-recognized anti-CTLA-4 antibodies can be used. For example, the anti-CTLA-4 antibodies disclosed in U.S. Patent No. 8,119,129, PCT Publication No. 01 / 14424, PCT Publication No. 98 / 42752, PCT Publication No. 00 / 37504 (CP675,206, also known as tremelimumab, formerly known as ticilimumab), U.S. Patent No. 6,207,156, Hurwitz et al. (1998) Proc Natl Acad Sci USA, 95(17): 10067-10071, Camacho et al. (2004) J Clin Oncology, 22(145): Abstract No. 2505 (antibody CP-675206), and Mokyr et al. (1998) Cancer Res, 58: 5301-5304 can be used in the methods disclosed herein.The teachings of each of the above publications are incorporated herein by reference. Antibodies that compete with any of these art-recognized antibodies for binding to CTLA-4 can also be used. For example, humanized CTLA-4 antibodies are described in International Patent Applications Nos. 2001 / 014424, 2000 / 037504, and U.S. Patent No. 8,017,114, all of which are incorporated herein by reference.

[0247] An exemplary anti-CTLA-4 antibody is ipilimumab (also known as 10D1, MDX-010, MDX-101, and Yervoy®) or antigen-binding fragments and variants thereof (see, e.g., WO01 / 14424). In other embodiments, the antibody comprises the heavy and light chain CDRs or VRs of ipilimumab. Thus, in one embodiment, the antibody comprises the CDR1, CDR2, and CDR3 domains of the VH region of ipilimumab and the CDR1, CDR2, and CDR3 domains of the VL region of ipilimumab. In another embodiment, the antibody competes for binding with and / or binds to the same epitope on CTLA-4 as the antibody. In another embodiment, the antibody has at least about 90% variable region amino acid sequence identity to the antibody (e.g., at least about 90%, 95%, or 99% variable region identity to ipilimumab). Other molecules for modulating CTLA-4 include CTLA-4 ligands and receptors such as those described in U.S. Pat. Nos. 5,844,905, 5,885,796, and International Patent Applications Nos. 1995 / 001994 and 1998 / 042752, all of which are incorporated herein by reference, and immunoadhesins such as those described in U.S. Pat. No. 8,329,867, which is incorporated herein by reference.

[0248] Another immune checkpoint protein that can be targeted in the methods provided herein is lymphocyte-activation gene 3 (LAG-3), also known as CD223. The complete protein sequence of human LAG-3 has Genbank accession number NP-002277. LAG-3 is found on the surface of activated T cells, natural killer cells, B cells, and plasmacytoid dendritic cells. LAG-3 functions as an "off" switch when bound to MHC class II on the surface of antigen-presenting cells. Inhibition of LAG-3 activates both effector T cells and inhibitory regulatory T cells. In some embodiments, the immune checkpoint inhibitor is an anti-LAG-3 antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide. Anti-human LAG-3 antibodies (or VH and / or VL domains derived therefrom) suitable for use in the present methods can be generated using methods well known in the art. Alternatively, art-recognized anti-LAG-3 antibodies can be used. An exemplary anti-LAG-3 antibody is leratolimab (also known as BMS-986016) or its antigen-binding fragments and variants thereof (see, e.g., WO2015 / 116539). Other exemplary anti-LAG-3 antibodies include TSR-033 (see, e.g., WO2018 / 201096), MK-4280, and REGN3767. MGD013 is an anti-LAG-3 / PD-1 bispecific antibody described in WO2017 / 019846. FS118 is an anti-LAG-3 / PD-L1 bispecific antibody described in WO2017 / 220569.

[0249] Another immune checkpoint protein that can be targeted in the methods provided herein is V-domain Ig suppressor of T-cell activation (VISTA), also known as C10orf54. The complete protein sequence of human VISTA has Genbank accession number NP_071436. VISTA is found in leukocytes and inhibits T-cell effector function. In some embodiments, the immune checkpoint inhibitor is an anti-VISTA antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide. Anti-VISTA antibodies (or VH and / or VL domains derived therefrom) suitable for use in the present methods can be generated using methods well known in the art. Alternatively, art-recognized anti-VISTA antibodies can be used. An exemplary anti-VISTA antibody is JNJ-61610588 (also known as onvatilimab) (see, e.g., WO2015 / 097536, WO2016 / 207717, WO2017 / 137830, WO2017 / 175058). VISTA can also be inhibited with the small molecule CA-170, which selectively targets both PD-L1 and VISTA (see, e.g., WO2015 / 033299, WO2015 / 033301).

[0250] Another metabolic protein with immune function that can be targeted by the methods provided herein is indoleamine 2,3-dioxygenase (IDO). The complete protein sequence of human IDO has Genbank accession number NP_002155. In some embodiments, the immune inhibitor is a small molecule IDO inhibitor. Exemplary small molecules include BMS-986205, epacadostat (INCB24360), and navoximod (GDC-0919).

[0251] Another immune checkpoint protein that can be targeted by the methods provided herein is CD38. The complete protein sequence of human CD38 has Genbank accession number NP_001766. In some embodiments, the immune checkpoint inhibitor is an anti-CD38 antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide. Anti-CD38 antibodies (or VH and / or VL domains derived therefrom) suitable for use in the present methods can be generated using methods well known in the art. Alternatively, art-recognized anti-CD38 antibodies can be used. An exemplary anti-CD38 antibody is daratumumab (see, e.g., U.S. Patent No. 7,829,673).

[0252] Another immune checkpoint protein that can be targeted by the methods provided herein is ICOS, also known as CD278. The complete protein sequence of human ICOS has Genbank accession number NP_036224. In some embodiments, the immune checkpoint inhibitor is an anti-ICOS antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide. Anti-ICOS antibodies (or VH and / or VL domains derived therefrom) suitable for use in the present methods can be generated using methods well known in the art. Alternatively, art-recognized anti-ICOS antibodies can be used. Exemplary anti-ICOS antibodies include JTX-2011 (see, e.g., WO2016 / 154177, WO2018 / 187191) and GSK3359609 (see, e.g., WO2016 / 059602).

[0253] Another immune checkpoint protein that can be targeted by the methods provided herein is T cell immunoreceptor (TIGIT) with Ig and ITIM domains. The complete protein sequence of human TIGIT has Genbank accession number NP_776160. In some embodiments, the immune checkpoint inhibitor is an anti-TIGIT antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide. Anti-TIGIT antibodies (or VH and / or VL domains derived therefrom) suitable for use in the present methods can be generated using methods well known in the art. Alternatively, art-recognized anti-TIGIT antibodies can be used. An exemplary anti-TIGIT antibody is MK-7684 (see, e.g., WO2017 / 030823, WO2016 / 028656).

[0254] Another immune checkpoint protein that can be targeted by the methods provided herein is OX40, also known as CD134. The complete protein sequence of human OX40 has Genbank accession number NP_003318. In some embodiments, the immune checkpoint inhibitor is an anti-OX40 antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide. Anti-OX40 antibodies (or VH and / or VL domains derived therefrom) suitable for use in the present methods can be generated using methods well known in the art. Alternatively, art-recognized anti-OX40 antibodies can be used. An exemplary anti-OX40 antibody is PF-04518600 (see, e.g., WO2017 / 130076). ATOR-1015 is a bispecific antibody that targets CTLA4 and OX40 (see, e.g., WO2017 / 182672, WO2018 / 091740, WO2018 / 202649, WO2018 / 002339).

[0255] Another immune checkpoint protein that can be targeted in the methods provided herein is glucocorticoid-induced tumor necrosis factor receptor-related protein (GITR), also known as TNFRSF18 and AITR. The complete protein sequence of human GITR has Genbank accession number NP_004186. In some embodiments, the immune checkpoint inhibitor is an anti-GITR antibody (e.g., a human antibody, a humanized antibody, or a chimeric antibody), an antigen-binding fragment thereof, an immunoadhesin, a fusion protein, or an oligopeptide. Anti-human GITR antibodies (or VH and / or VL domains derived therefrom) suitable for use in the present methods can be generated using methods well known in the art. Alternatively, art-recognized anti-GITR antibodies can be used. An exemplary anti-GITR antibody is TRX518 (see, e.g., WO2006 / 105021).

[0256] In some embodiments, immunotherapy can be adoptive immunotherapy, involving the transfer of ex vivo generated autoantigen-specific T cells. T cells used in adoptive immunotherapy can be generated either by expansion of antigen-specific T cells or by redirection of T cells through genetic engineering (Park, Rosenberg et al. 2011). Isolation and transfer of tumor-specific T cells has been shown to be successful in treating melanoma. Novel specificities in T cells have been successfully generated through the gene transfer of transgenic T cell receptors or chimeric antigen receptors (CARs) (Jena, Dotti et al. 2010). CARs are synthetic receptors consisting of a targeting moiety associated with one or more signaling domains in a single fusion molecule. Generally, the binding portion of a CAR consists of the antigen-binding domain of a single-chain antibody (scFv), which contains the light chain and variable fragment of a monoclonal antibody joined by a flexible linker. Binding moieties based on receptor or ligand domains have also been successfully used. The signaling domain in first-generation CARs is derived from the cytoplasmic region of CD3 zeta or the Fc receptor gamma chain. CARs have been successfully used to redirect T cells against antigens expressed on the surface of tumor cells from a variety of malignancies, including lymphomas and solid tumors (Jena, Dotti et al. 2010).

[0257] In one embodiment, the present application provides a combination therapy for the treatment of cancer, the combination therapy comprising adoptive T cell therapy and a checkpoint inhibitor. In one aspect, the adoptive T cell therapy comprises autologous and / or allogeneic T cells. In another aspect, the autologous and / or allogeneic T cells target tumor antigens.

[0258] D.Surgery Approximately 60% of patients with cancer undergo some type of surgery, including preventive, diagnostic, staging, curative, and palliative surgery. Curative surgery includes resection, in which all or part of the cancerous tissue is physically removed, excised, and / or destroyed, and may be used in conjunction with other therapies, such as the treatment of the present invention, chemotherapy, radiation therapy, hormone therapy, gene therapy, immunotherapy, and / or alternative therapies. Tumor resection refers to the physical removal of at least part of the tumor. In addition to tumor resection, surgical treatments include laser surgery, cryosurgery, electrosurgery, and microsurgery (Mohs surgery).

[0259] The removal of part or all of the cancerous cells, tissue, or tumor may result in the formation of a cavity in the body. Treatment may be achieved by perfusion, direct injection, or local application of additional anti-cancer therapy to the site. Such treatment may be repeated, for example, every 1, 2, 3, 4, 5, 6, or 7 days, or every 1, 2, 3, 4, and 5 weeks, or every 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 months. These treatments may also be at various dosages.

[0260] E. Other drugs It is contemplated that other agents may be used in combination with certain aspects of the present embodiment to improve the therapeutic efficacy of the treatment. These additional agents include agents that affect the upregulation of cell surface receptors and GAP junctions, cytostatic and differentiation agents, cell adhesion inhibitors, agents that sensitize hyperproliferative cells to apoptosis inducers, or other biological agents. Increasing intercellular signaling by increasing the number of GAP junctions increases the anti-hyperproliferative effect on adjacent hyperproliferative cell populations. In other embodiments, cytostatic or differentiation agents may be used in combination with certain aspects of the present embodiment to improve the anti-hyperproliferative efficacy of the treatment. Cell adhesion inhibitors are contemplated to improve the efficacy of the present embodiment. Examples of cell adhesion inhibitors are focal adhesion kinase (FAK) inhibitors and lovastatin. Furthermore, it is contemplated that other agents that sensitize hyperproliferative cells to apoptosis, such as the antibody c225, may be used in combination with certain aspects of the present embodiment to improve the therapeutic efficacy.

[0261] VI. Detection Methods In some embodiments, the present disclosure relates to immunodetection methods for detecting B7-H3 expression. A wide variety of assay formats are contemplated for detecting protein products, including immunohistochemistry, enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), immunoradiometric assay, fluorescent immunoassay, chemiluminescence assay, bioluminescence assay, dot blotting, FACS analysis, mass cytometry (CyTOF), imaging mass cytometry (IMC), and Western blot, to name a few. The steps of various useful immunodetection methods are described in the scientific literature. In general, immunobinding methods involve obtaining a sample and contacting the sample with an antibody specific to the protein to be detected, optionally under conditions effective to allow the formation of an immune complex. In general, detection of immune complex formation is well known in the art and can be achieved by applying a number of approaches. These methods are generally based on the detection of labels or markers, such as radioactive, metallic, fluorescent, biological, and enzymatic tags. Detection methods may include ex vivo imaging, such as CyTOF or IMC. Alternatively, detection methods may involve in vivo imaging, such as PET or SPECT imaging. Of course, as is known in the art, further advantages may be found through the use of a second antibody and / or a second binding ligand, such as a biotin / avidin ligand binding arrangement.

[0262] The antibody used for detection can itself be conjugated to a detectable label, which can then be easily detected, thereby allowing the amount of primary immune complexes in the composition to be determined. Alternatively, the first antibody that becomes bound within the primary immune complex can be detected by a second binding ligand that has binding affinity for the antibody. In these cases, the second binding ligand can be conjugated to a detectable label. The second binding ligand is often itself an antibody and can therefore be called a "secondary" antibody. The primary immune complexes are contacted with a labeled second binding ligand or antibody under conditions and for a period of time sufficient to allow the formation of secondary immune complexes. The secondary immune complexes are then generally washed to remove any non-specifically bound labeled second antibody or ligand, and the label remaining in the secondary immune complexes is then detected.

[0263] In some embodiments, the present disclosure provides imaging methods using the compounds and compositions of the present disclosure. In some embodiments, the imaging is positron emission tomography. Positron emission tomography (PET) imaging is based on detecting two simultaneous high-energy photons from the emission of positron-emitting radioisotopes. PET imaging is unparalleled in its extremely high sensitivity and accurate assessment of the in vivo concentration of radiotracers. PET imaging has been widely adopted as an important clinical modality for oncological, cardiovascular, and neurological applications. PET imaging has also become an important tool in preclinical studies, especially for investigating murine and other small animal models of disease.

[0264] As used herein, the term "sample" refers to any sample suitable for the detection methods provided by the present invention. A sample can be any sample containing material suitable for detection or isolation. Sample sources include blood, pleural fluid, peritoneal fluid, urine, saliva, malignant ascites, bronchopulmonary lavage fluid, synovial fluid, and bronchial washings. In one embodiment, the sample is a blood sample, for example, including whole blood or any fraction or component thereof. Blood samples suitable for use in the present invention can be extracted from any known source containing blood cells or components thereof, such as venous, arterial, peripheral, tissue, umbilical cord, etc. For example, samples can be obtained and processed using well-known and routine clinical methods (e.g., procedures for collecting and processing whole blood). In one embodiment, an exemplary sample can be peripheral blood collected from a subject with cancer. In some embodiments, a biological sample contains a plurality of cells. In certain embodiments, a biological sample comprises fresh or frozen tissue. In certain embodiments, a biological sample comprises formalin-fixed, paraffin-embedded tissue. In some embodiments, the biological sample is a tissue biopsy, fine needle aspirate, blood, serum, plasma, cerebrospinal fluid, urine, feces, saliva, circulating tumor cells, exosomes, or bodily secretions such as aspirates and sweat. In some embodiments, the biological sample contains cell-free DNA.

[0265] VII. Formulations and Routes of Administration In another embodiment, for administration to a patient in need of diagnostic evaluation and / or treatment, a radiopharmaceutical formulation (also referred to as a radiopharmaceutical preparation, radiopharmaceutical composition, radiopharmaceutical, or radiopharmaceutical product) comprises a diagnostically or therapeutically effective amount of a radiolabeled compound disclosed herein formulated with one or more excipients and / or drug carriers appropriate for the indicated route of administration.

[0266] In some embodiments, the radiolabeled compounds disclosed herein are formulated in a manner acceptable for diagnostic evaluation or treatment of human and / or veterinary subjects. In some embodiments, the formulation comprises mixing or combining one or more of the radiolabeled compounds disclosed herein with one or more of the following excipients: lactose, sucrose, starch powder, cellulose esters of alkanoic acids, cellulose alkyl esters, talc, stearic acid, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphate and sulfate, gelatin, acacia, sodium alginate, polyvinylpyrrolidone, and / or polyvinyl alcohol. In some embodiments, the compounds may be dissolved or slurried in water, polyethylene glycol, propylene glycol, ethanol, corn oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride, and / or various buffers. In some embodiments, pharmaceutical formulations may be subjected to pharmaceutical operations such as sterilization and / or may contain drug carriers and / or excipients such as preservatives, stabilizers, wetting agents, emulsifiers, encapsulating agents such as lipids, dendrimers, polymers, proteins such as albumin, nucleic acids, and buffers.

[0267] Radiopharmaceutical formulations can be administered by various methods, such as injection (e.g., subcutaneous, intravenous, intratumoral, and intraperitoneal). Depending on the route of administration, the radiolabeled compounds disclosed herein can be administered to patients in an appropriate carrier, such as liposomes, or a diluent. Pharmaceutically acceptable diluents include saline and aqueous buffer solutions. Liposomes include water-in-oil-in-water CGF emulsions and conventional liposomes. The radiolabeled compounds disclosed herein can also be administered parenterally, intraperitoneally, intratumorally, intraspinally, or intracerebrally. Dispersions can be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof, as well as in oils. Under ordinary conditions of storage and use, these preparations may contain a preservative to prevent the growth of microorganisms.

[0268] Radiopharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (such as glycerol, propylene glycol, and liquid polyethylene glycol), suitable mixtures thereof, and vegetable oils. Proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants. Prevention of microbial action can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it is preferable to include isotonic agents, for example, sugars, sodium chloride, or polyalcohols such as mannitol and sorbitol, in the composition. Prolonged absorption of injectable compositions can be achieved by including in the composition an agent that delays absorption, for example, aluminum monostearate or gelatin.

[0269] In some embodiments, it may be advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. As used herein, dosage unit form refers to physically discrete units suitable as a single dose for a patient to be treated, each unit containing a predetermined amount of radiopharmaceutical calculated to produce a desired imaging effect in association with the necessary pharmaceutical carrier. In some embodiments, the specifications for the dosage unit forms of the present disclosure are determined by and directly depend on (a) the unique characteristics of the radiopharmaceutical and the particular imaging effect to be achieved, and (b) the limitations inherent in the art of formulating such radiopharmaceuticals for patient imaging. In some embodiments, the active compound is administered at an effective dose sufficient to generate PET images of immune activity in a patient. For example, the efficacy of the compound can be evaluated in an animal model system that can predict efficacy for imaging immune activity in humans or another animal.

[0270] VIII. Kit In various aspects of the present embodiment, kits containing therapeutic and / or other therapeutic agents and delivery agents are contemplated. In some embodiments, kits are provided for preparing and / or administering the therapies of the embodiments. The kits may include one or more sealed vials containing any of the pharmaceutical compositions of the present embodiments. The kits may include, for example, at least one B7-H3 antibody or B7-H3-specific CAR construct, as well as reagents for preparing, formulating, and / or administering the components of the embodiments or performing one or more steps of the methods of the present invention. In some embodiments, the kits may also include suitable containers that do not react with the components of the kit, such as Eppendorf tubes, assay plates, syringes, bottles, or tubes. The containers may be made of sterilizable materials such as plastic or glass.

[0271] The kits may further include instructions outlining the procedural steps of the methods set forth herein, following substantially the same procedures described herein or known to those of skill in the art. The instructional information may be present in a computer-readable medium containing machine-readable instructions that, when executed using a computer, cause the display of a real or virtual procedure for delivering a pharmaceutically effective amount of a therapeutic agent. [Example]

[0272] IX. Working Example The following examples are included to demonstrate preferred embodiments of the invention. It should be understood by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventors to function well in the practice of the invention, and as such can be considered to constitute preferred modes for its practice. However, those skilled in the art will, in light of the present disclosure, understand that numerous changes can be made in the specific embodiments which are disclosed and still obtain like or similar results without departing from the spirit and scope of the invention.

[0273] Example 1 Generation of Therapeutic Antibodies Targeting B7-H3 New Zealand Black / White F1 hybrid mice (NZBWF1 / J, Jackson Labs, stock no. 100008) were used to generate antibodies against B7-H3. NZBW mice are widely used as a model for autoimmune diseases similar to human systemic lupus erythematosus (SLEU), resulting in elevated levels of immunoglobulins, antinuclear antibodies, antithymocyte antibodies, and severe, progressive glomerulonephritis. These autoimmune characteristics arise from defective self-tolerance. Here, the disrupted tolerance to self-antigens in the NZBWF1 / J strain was exploited by vaccinating animals with a suitable source containing cells expressing both murine and human B7-H3, ensuring that candidate murine autoantibodies against B7-H3 epitopes or biosimilars are not eliminated by host immune processing. Therefore, the probability of recovering high-affinity monoclonal antibodies from serum that react with both human (foreign) and murine (self) epitopes was increased.

[0274] Murine L cells (ATCC) were engineered to express human 4Ig-B7-H3 on the cell surface in addition to native murine 2Ig-B7-H3 by transduction with a custom lentivirus encoding human 4Ig-B7-H3 (GeneCopoeia, Inc.). 10 × 10 total cells were injected into NZBWF1 / J mice. 6 Six rounds of inoculations yielded 1,440 hybridoma clones. Screening yielded 14 candidate hybridoma cell lines that were found to bind to 4Ig-B7-H3L cells by standard ELISA immunoscreening. Of these candidates, secondary testing of the supernatant on HeLa cells (which express high levels of human 4Ig-B7-H3) yielded one high-affinity candidate. After expansion and antibody purification, further analysis by biolayer interferometry resulted in the discovery and characterization of MIL33B as a candidate with pM affinity for human 4Ig-B7-H3 and nM affinity for murine 2Ig-B7-H3.

[0275] The MIL33B hybridoma pellet was frozen and sent to a sequencing core facility (Vanderbilt Sequencing Center, Nashville, TN) for sequencing of both the heavy and light chain hypervariable regions. The isotype of MIL33B has been determined to be IgG2a. The complementarity-determining regions (CDRs) and variable regions of the MIL33B antibody are provided in Tables 1-3.

[0276] Table 1. CDRs of variable sequences of MIL33B antibody predicted by IMGT / DomainGapAlign (Ehrenmann et al., 2010; Ehrenmann & Lefranc, 2011). TIFF0007779484000002.tif29150

[0277] Table 2. CDRs of variable sequences of MIL33B antibody predicted by Paratome (Kunik et al., 2012a, Kunik et al., 2012b). TIFF0007779484000003.tif29150

[0278] Table 3: CDRs of variable sequences of MIL33B antibody predicted by Chothia TIFF0007779484000004.tif29150

[0279] Table 4: Protein sequences in the MIL33B variable region TIFF0007779484000005.tif41150

[0280] Table 5: Nucleotide sequences in the MIL33B variable region TIFF0007779484000006.tif82150

[0281] Example 2 MIL33B binds to human 4Ig-B7-H3 with pM affinity The in vitro binding affinity of MIL33B for human 4Ig-B7-H3 and murine 2Ig-B7-H3 was evaluated by ELISA. The extracellular domains of human 4Ig-B7-H3 and murine 2Ig-B7-H3 were purchased and added to a 96-well plate. The plate was then incubated with various concentrations of purified MIL33B. The plate was then washed and antibody binding was assessed via absorbance measurements. This experiment was completed for three independent preparations and purifications of MIL33B. The EC50 for each curve for each lot was calculated and plotted (logarithmic plot) (Figure 1). MIL33B has picomolar affinity for human 4Ig-B7-H3 and nanomolar affinity for murine 2Ig-B7-H3.

[0282] Example 3 MIL33B selectively binds to human 4Ig-B7-H3 The extracellular domains of the indicated B7 family proteins were purchased from R&D Systems. All proteins were verified by the vendor to be both pure and functional. Kd values ​​were determined using capture biolayer interferometry (Octet, Molecular Devices) in "affinity" mode, where the MIL33B antibody was captured on the tip of a probe and placed in a solution containing different concentrations of the target extracellular domain. Kd, Kd error, and R 2 The values ​​are reported in Table 6. An example of a fitted diagram of MIL33B binding to human 4Ig-B7-H3 is shown in Figure 2. These data show that MIL33B binds to 4Ig-B7-H3 at least 1000-fold better than other B7 family members.

[0283] Table 6. Binding of MIL33B to various B7 family members TIFF0007779484000007.tif70150

[0284] Example 4 Fluorescently Labeled MIL33B Selectively Binds to B7-H3-Expressing Cells Compared to Isotype Control Using live-cell immunofluorescence microscopy, we demonstrated selective, blockable binding of MIL33B to both human and murine B7-H3 expressed in tumor cells. 4T1 cells (ATCC), a murine breast tumor, were stably transduced with human 4Ig-B7-H3 or an empty vector using lentiviral constructs. Cells were selected that showed levels of 4Ig-B7-H3 expression consistent with those found endogenously in human solid tumors known to express B7-H3, such as cervical carcinoma (HeLa) or colorectal carcinoma (HCT116) (Figure 3). These engineered cells provide relevant models.

[0285] MIL33B or isotype control IgG2a was labeled with Alexa594 fluorophore at 1 mg / mL using a commercially available kit (Life Technologies) and purified through a size-exclusion column. The resulting product was designated MIL33B-A594 or IgG2a-A594. Labeling yield was quantified by UV / Vis spectroscopy.

[0286] Cells expressing human 4Ig-B7-H3 were incubated with either labeled MIL33B (1 μg / mL) or murine isotype control IgG2a (1 μg / mL) alone for 1 hour at 37°C. Blocking experiments were performed by incubating cells with 50 μg / mL unlabeled MIL33B before adding 1 μg / mL MIL33B-A594. Cells were washed and imaged by fluorescence microscopy (TiE, Nikon). Antibody binding (red) was co-depicted with nuclear staining (blue) (Figure 4A and B).

[0287] Pan02 cells, a pancreatic tumor of murine origin known to express murine 2Ig-B7-H3, were similarly imaged with MIL33B-A594 using 100 μg / mL MIL33B-A594, reflecting an approximately 100-fold shift in Kd from human 4Ig-B7-H3 to murine 2Ig-B7-H3 (Fig. 4C).

[0288] Example 5 Flagellin-conjugated MIL33B induces the NF-κB pathway via TLR5 MIL33B conjugated to the TLR5 agonist flagellin maintained nM binding affinity and was able to induce inflammatory pathways, such as NF-κB, through TLR5 in live-cell assays.

[0289] Purified flagellin (InvivoGen) was conjugated to MIL33B via a commercially available linker kit (see figure). Conjugation was verified by UV-Vis spectroscopy, and dual Western blot analysis confirmed that >90% of the antibody was conjugated to higher molecular weight species, which also contained flagellin (Figure 5). A loss of affinity is expected upon conjugation of the antibody to a ligand. Due to the antibody's initial pM affinity, the conjugate maintained an EC50 of 36 nM against human 4Ig-B7-H3 after conjugation to flagellin, as determined by ELISA (Figure 5, right panel).

[0290] HCT116 cells expressing endogenous human 4Ig-B7-H3 and TLR5, the native cognate receptor for flagellin, were stably transduced with the κB-RE5-IκBα-Fluc reporter. This cell line allows for the examination of both IκBα activation via initial degradation of the IκBα-luciferase (IκBα-Fluc) fusion protein, as readout by loss of light production, and subsequent activation of NF-κB transcriptional targets via resynthesis of IκBα-Fluc, as readout by a secondary increase in light production from the κB response element (RE5) (Figure 6A-B). The MIL33B-flgn conjugate was able to induce NF-κB activation via TLR5 at 18.2 nM, with a response potency similar to that of 1.8 nM purified flagellin (Figure 6C-D). Therefore, MIL33B conjugates can be used for tumor-specific delivery of immune stimulators to the tumor microenvironment.

[0291] Example 6 MIL33B mAb was conjugated with DFO 89Radiolabeling with Zr allows selective detection of tumor expression of human 4Ig-B7-H3 in syngeneic animal tumor models by PET imaging. MIL33B was radiolabeled with Zr-89 for PET imaging of B7-H3-expressing tumors and demonstrated robust signal-to-noise ratios in two different immunocompetent syngeneic murine tumor models.

[0292] MIL33B (blue) or IgG2a isotype control (red) antibodies were conjugated with DFO using standard conjugation methods. MIL33B-DFO or IgG2a-DFO 89 Radiolabeling was performed by incubation with Zr in acetate buffer (pH 7) for 1 hour and purified by size-exclusion chromatography. Labeling was confirmed by radio-TLC.

[0293] We utilized immunocompetent mice bearing subcutaneous 4T1 tumors expressing human 4Ig-B7-H3 or a negative vector (see Western blot in Figure 3). The 4T1 tumors also contained low but detectable levels of murine 2Ig (see Western blot in Figure 3). Mice were intravenously injected with approximately 30 μCi of radiolabeled MIL33B antibody or an IgG2a control antibody and imaged 24 and 72 hours postinjection using a dedicated small-animal PET / SPECT / CT scanner (Albira, Bruker Corp). Similarly, B16F10 cells were transduced with human 4Ig-B7-H3 or an empty vector. These cells contained less endogenous murine 2Ig-B7H3 than 4T1 tumors. MIL33B was both qualitatively and quantitatively superior to the isotype control for binding to tumors expressing human 4Ig-B7-H3, giving the correct rank order of binding for the negative vector, as predicted by their low background murine 2Ig-B7-H3 expression levels (Fig. 7).

[0294] Example 7 MIL33B mAb monotherapy cured aggressive ICT-resistant humanized B16F10 tumors Administration of MIL33B antibody (ip) demonstrated therapeutic potential as a single-agent immunotherapy in a highly ICT-resistant syngeneic murine breast cancer model.

[0295] Murine B16F10 melanoma tumors represent a non-inflammatory "cold" tumor type and are known to be resistant to combination immune checkpoint therapy (ICT) when treated with both anti-PD-1 and anti-CTLA-4. Humanized B16F10 tumors (as described above), engineered to express endogenous levels of human B7-H3, were implanted subcutaneously into immunocompetent C57B16 mice using 10,000 cells per implant. On days 3, 6, and 9 after tumor inoculation, mice were treated with either PBS alone (n=5, i.p.) or 200 μg, 100 μg, and 100 μg / mouse of MIL33B (n=10, i.p.), respectively. Mice were then followed until day 150 after inoculation. Mice were euthanized when the maximum tumor axis was >1.5 cm, when tumor ulceration was >3 mm, or when the mice were moribund as determined by independent veterinary staff. Overall survival curves and individual tumor growth curves are shown in FIG.

[0296] All of the methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of the present invention have been described in terms of preferred embodiments, it will be apparent to those skilled in the art that modifications can be applied to the methods and method steps or sequence of steps described herein without departing from the concept, spirit, and scope of the invention. More specifically, it will be apparent that certain agents that are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope, and concept of the invention as defined by the appended claims.

[0297] References The following references, to the extent that they provide exemplary procedural or other details supplementary to those set forth herein, are specifically incorporated herein by reference. TIFF0007779484000008.tif182150TIFF0007779484000009.tif86150

Claims

1. A monoclonal antibody or antibody fragment thereof, wherein the monoclonal antibody or antibody fragment thereof comprises a heavy chain variable region (VH) comprising VHCDR1, VHCDR2, and VHCDR3 amino acid sequences derived from SEQ ID NO: 7, and a light chain variable region (VL) comprising VLCDR1, VLCDR2, and VLCDR3 amino acid sequences derived from SEQ ID NO: 8, and is capable of binding to B7-H3.

2. (a) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 1, a VHCDR2 amino acid sequence comprising SEQ ID NO: 2, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 3; and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 4, a VLCDR2 amino acid sequence comprising SEQ ID NO: 5, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6; (b) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 11, a VHCDR2 amino acid sequence comprising SEQ ID NO: 12, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 13, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 14, a VLCDR2 amino acid sequence comprising SEQ ID NO: 15, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 16; (c) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 17, a VHCDR2 amino acid sequence comprising SEQ ID NO: 18, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 19, and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 20, a VLCDR2 amino acid sequence comprising SEQ ID NO: 21, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 6; or (d) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 17, a VHCDR2 amino acid sequence comprising SEQ ID NO: 18, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 19; and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 4, a VLCDR2 amino acid sequence comprising SEQ ID NO: 5, and a VLCDR3 amino acid sequence comprising SEQ ID NO:

6. The monoclonal antibody or antibody fragment thereof according to claim 1, comprising:

3. A monoclonal antibody or antibody fragment thereof according to claim 1 or 2, comprising a heavy chain variable sequence having at least 70% identity to SEQ ID NO: 7 and a light chain variable sequence having at least 70% identity to SEQ ID NO:

8.

4. The monoclonal antibody or antibody fragment thereof according to any one of claims 1 to 3, which is a humanized antibody.

5. The antibody fragment may be a monovalent scFv (single chain fragment variable) antibody, a bivalent scFv, a Fab fragment, an F(ab') ２ Fragment, F(ab') ３ The monoclonal antibody or antibody fragment thereof according to any one of claims 1 to 4, which is a fragment, Fv fragment, or single-chain antibody.

6. The monoclonal antibody or antibody fragment thereof according to any one of claims 1 to 5, wherein the antibody is a chimeric antibody, a bispecific antibody, or a BiTE, and / or the antibody is an IgG antibody or a recombinant IgG antibody or an antibody fragment thereof.

7. The monoclonal antibody or antibody fragment thereof according to any one of claims 1 to 6, wherein the antibody is conjugated or fused to an imaging agent, a cytotoxic agent, a metal, or a radioactive moiety.

8. The monoclonal antibody or antibody fragment thereof of claim 7, wherein the imaging agent is a fluorophore.

9. 8. The monoclonal antibody or antibody fragment thereof of claim 7, wherein the radioactive moiety is Zr-89, Cu-64, F-18, Y-90, Lu-177, At-211, Ac-225, or Pb-212.

10. The monoclonal antibody or antibody fragment thereof according to any one of claims 1 to 6, wherein the antibody is an immunoconjugate.

11. The monoclonal antibody or antibody fragment thereof of claim 10, wherein the antibody is conjugated to flagellin or a flagellin derivative.

12. The monoclonal antibody or antibody fragment thereof according to any one of claims 1 to 6, wherein the antibody is an antibody-drug conjugate.

13. An isolated nucleic acid encoding the antibody heavy and / or light chain variable region of the antibody molecule of any one of claims 1 to 6.

14. A hybridoma or engineered cell comprising a nucleic acid encoding the antibody or antibody fragment thereof according to any one of claims 1 to 6, or the nucleic acid according to claim 13.

15. A pharmaceutical formulation comprising one or more antibodies or antibody fragments thereof according to any one of claims 1 to 12.

16. 16. The pharmaceutical preparation of claim 15 for treating cancer in a patient.

17. 13. A method for determining whether a patient with cancer has a cancer that expresses B7-H3, the method comprising the steps of contacting cancer tissue obtained from the patient with the antibody or antibody fragment thereof according to any one of claims 1 to 12, and detecting binding of the antibody or antibody fragment thereof to the tissue, wherein the binding of the antibody or antibody fragment thereof to the tissue indicates that the patient has a cancer that expresses B7-H3.

18. 18. A method of aiding in the selection of a patient having cancer for treatment with an anti-B7-H3 antibody, comprising determining whether the cancer expresses B7-H3 by the method of claim 17, wherein expression of B7-H3 by the cancer indicates that the patient should be selected for treatment with an anti-B7-H3 therapy.

19. 13. A method for detecting the presence of B7-H3 on the surface of a cell, in a tissue, in an organ, or in a biological sample, ex vivo or in vitro, comprising: (a) contacting the cell, tissue, organ, or biological sample with an antibody of any one of claims 1-12; and (b) detecting the presence of the antibody bound to the cell, tissue, organ, or sample.

20. A composition for use in detecting the presence of B7-H3 in vivo on the surface of a cell, in a tissue, in an organ, or in a biological sample, the composition comprising one or more antibodies or antibody fragments thereof described in any one of claims 1 to 12.

Images