Bispecific antibodies
US-2016145355-A1 · May 26, 2016 · US
US10457732B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10457732-B2 |
| Application number | US-201715588271-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 5, 2017 |
| Priority date | May 6, 2016 |
| Publication date | Oct 29, 2019 |
| Grant date | Oct 29, 2019 |
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The disclosure generally provides proteins that bind two epitopes (e.g., a first and a second epitope) and that are bivalent for binding to each of the first and second epitopes. The disclosure also provides for specific binding proteins, including antibodies, which bind to a target protein. The disclosure also provides compositions comprising such proteins, nucleic acid molecules encoding such proteins and methods of making such proteins. The disclosure provides methods of inducing an immune response in a subject as well as methods for treating or preventing cancer in a subject by administering the proteins, nucleic acid molecules and/or compositions to the subject.
Opening claim text (preview).
What is claimed is: 1. A bispecific binding protein that binds to PD-1 and CTLA-4 comprising a first heavy chain comprising the amino acid sequence of SEQ ID NO: 9, a first light chain comprising the amino acid sequence of SEQ ID NO: 7, a second heavy chain comprising the amino acid sequence of SEQ ID NO: 12, and a second light chain comprising the amino acid sequence of SEQ ID NO: 4. 2. The protein of claim 1 comprising an Fc region, wherein the Fc region is aglycosylated. 3. The protein of claim 1 comprising an Fc region, wherein the Fc region is deglycosylated. 4. The protein of claim 1 comprising an Fc region, wherein the Fc region has reduced fucosylation or is afucosylated. 5. A composition comprising the protein of claim 1 and a pharmaceutically acceptable carrier. 6. A nucleic acid molecule comprising a nucleotide sequence encoding a protein of claim 1 . 7. A vector comprising the nucleic acid molecule of claim 6 . 8. An isolated host cell comprising the vector of claim 7 . 9. A method of treating or preventing cancer in a subject, the method comprising administering the protein of claim 1 to the subject. 10. The method of claim 9 , wherein the cancer is one or more of ovarian cancer, breast cancer, colorectal cancer, prostate cancer, cervical cancer, uterine cancer, testicular cancer, bladder cancer, head and neck cancer, melanoma, pancreatic cancer, renal cell carcinoma, and lung cancer. 11. A method of enhancing an immune response in a subject, the method comprising administering the protein of claim 1 to the subject. 12. The nucleic acid molecule of claim 6 , wherein the nucleotide encoding the protein of claim 1 comprises a nucleotide sequence encoding a first heavy chain, comprising the nucleotide sequence of SEQ ID NO: 10; a nucleotide sequence encoding a first light chain, comprising the nucleotide sequence of SEQ ID NO: 8; a nucleotide sequence encoding a second heavy chain, comprising the nucleotide sequence of SEQ ID NO: 13; and a nucleotide sequence encoding a second light chain, comprising the nucleotide sequence of SEQ ID NO: 11.
Antibody-dependent cellular cytotoxicity [ADCC] · CPC title
Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity · CPC title
against the immunoglobulin superfamily · CPC title
Antineoplastic agents · CPC title
comprising antibodies · CPC title
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