IP Library Granted Patent US 12,428,472
Granted Patent B2
US 12,428,472 · App. 18/597,018 · Granted Sep 30, 2025

Human immunodeficiency virus neutralizing antibodies and methods of use thereof

Inventors: Johannes Scheid (New York, NY); Michel Nussenzweig (New York, NY); Pamela J. Bjorkman (Altadena, CA); Ron Diskin (Rehovot, IL)
Assignees: The Rockefeller University; California Institute of Technology
C07K16/1045C07K16/1063G01N33/56983A61K2039/505C07K2317/10C07K2317/21C07K2317/34C07K2317/55C07K2317/56C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 12,428,472
App. No.
18/597,018
Granted
Sep 30, 2025
Kind
B2
Abstract

The invention provides broadly neutralizing antibodies directed to epitopes of Human Immunodeficiency Virus, or HIV. The invention further provides compositions containing HIV antibodies used for prophylaxis, and methods for diagnosis and treatment of HIV infection.

Claims (32)

1. A non-naturally occurring anti-HIV gp120 antibody or antigen binding fragment thereof, comprising a heavy chain variable region (VH) comprising the amino acid sequence of SEQ ID NO: 892, and a light chain variable region (VL) comprising the amino acid sequence of SEQ ID NO: 906.

2. The anti-HIV antibody or antigen binding fragment thereof of claim 1 , wherein the antigen binding fragment is selected from the group consisting of Fab, Fab′, F(ab′)2, Fv, sFv and scFv.

3. The anti-HIV antibody or antigen binding fragment thereof of claim 1 , wherein the antibody is a recombinant antibody.

4. The anti-HIV antibody or antigen binding fragment thereof of claim 1 , wherein the antibody or antigen binding fragment thereof is formatted for prolonged serum half life.

5. The anti-HIV antibody of claim 1 , wherein the antibody is an immunoglobulin class or isotype selected from the group consisting of IgG1, IgG2, IgG3, IgG4, IgA, IgD, IgE and IgM.

6. A nucleic acid molecule comprising a sequence encoding the anti-HIV antibody or antigen binding fragment thereof of claim 1 .

7. A vector comprising the nucleic acid molecule of claim 6 .

8. A cultured cell comprising the vector of claim 7 .

9. A method for making an anti-HIV antibody or a fragment thereof, comprising:

obtaining the cultured cell of claim 8 ;

culturing the cell in a medium under conditions permitting expression of a polypeptide encoded by the vector and assembling of an antibody or fragment thereof; and

purifying the antibody or fragment from the cultured cell or the medium of the cell.

10. A pharmaceutical composition comprising (i) the anti-HIV antibody or antigen binding fragment thereof of claim 1 and (ii) a pharmaceutically acceptable carrier.

11. The pharmaceutical composition of claim 10 , further comprising a second therapeutic agent.

12. The pharmaceutical composition of claim 11 , wherein the second therapeutic agent comprises a second anti-HIV antibody or antigen binding fragment thereof.

13. The pharmaceutical composition of claim 12 , wherein the second therapeutic agent comprises an antiviral agent.

14. The pharmaceutical composition of claim 13 , wherein the antiviral agent is selected from the group consisting of a non-nucleoside reverse transcriptase inhibitor, a protease inhibitor, an entry or fusion inhibitor, and an integrase inhibitor.

15. A method of treating an HIV infection or an HIV-related disease comprising the steps of:

identifying a patient in need of such treatment, and

administering to said patient the pharmaceutical composition of claim 10 .

16. A method of treating an HIV infection or an HIV-related disease comprising the steps of:

identifying a patient in need of such treatment, and

administering to said patient a therapeutically effective amount of at least one isolated anti-HIV antibody or antigen binding fragment thereof of claim 1 .

17. The method of claim 16 , further comprising administering to said patient a second therapeutic agent.

18. The method of claim 17 , wherein the second therapeutic agent comprises a second anti-HIV antibody or antigen binding fragment thereof.

19. The method of claim 18 , wherein said second therapeutic agent comprises an antiviral agent.

20. The method of claim 19 , wherein the antiviral agent is selected from the group consisting of a non-nucleoside reverse transcriptase inhibitor, a protease inhibitor, an entry or fusion inhibitor, and an integrase inhibitor.

21. A kit comprising:

a pharmaceutically acceptable dose unit of a pharmaceutically effective amount of the anti-HIV antibody of claim 1 , and

a pharmaceutically acceptable dose unit of a pharmaceutically effective amount of an anti-HIV agent.

22. The kit of claim 21 , wherein the two pharmaceutically acceptable dose units take the form of a single pharmaceutically acceptable dose unit.

23. The kit of claim 22 , wherein the anti-HIV agent is selected from the group consisting of a non-nucleoside reverse transcriptase inhibitor, a protease inhibitor, an entry or fusion inhibitor, and an integrase inhibitor.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 5, 2025
From: SCHEID, JOHANNES; NUSSENZWEIG, MICHEL
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 071328/0135 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 5, 2025
From: BJORKMAN, PAMELA J.; DISKIN, RON
To: CALIFORNIA INSTITUTE OF TECHNOLOGY
Reel/Frame 071328/0364 →
Continuity (6)
Continuation 18172836 · Feb 22, 2023
Continuation 17248143 · Jan 11, 2021
Continuation 15719738 · Sep 29, 2017
Division 14118496
Provisional Application 61486960 · May 17, 2011
Related Publication 20240254206A1 · Aug 1, 2024
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