IP Library Granted Patent US 11,236,152
Granted Patent B2
US 11,236,152 · App. 15/772,443 · Granted Feb 1, 2022

Neutralizing antibodies to HIV-1 GP41 and their use

Inventors: Peter Kwong (Washington, DC); Young Do Kwon (Kensington, MD); Ivelin Georgiev (Nashville, TN); Gilad Ofek (Gaithersburg, MD); Baoshan Zhang (Bethesda, MD); Krisha McKee (Columbia, MD); John Mascola (Rockville, MD); Mark Connors (Bethesda, MD); Gwo-Yu Chuang (Rockville, MD); Sijy O'Dell (Silver Spring, MD); Robert Bailer (Adamstown, MD); Mark Louder (Mt. Airy, MD); Mangaiarkarasi Asokan (Rockville, MD); Richard Schwartz (Bethesda, MD); Jonathan Cooper (Arlington, VA); Kevin Carlton (Gaithersburg, MD); Michael Bender (Washington, DC); Amarendra Pegu (Potomac, MD); Lawrence Shapiro (New York, NY); Tatyana Gindin (New York, NY); Lisa Kueltzo (Gaithersburg, MD)
Assignees: The United States of America, as represented by the Sectetary, Department of Health and Human Services; The Trustees of Columbia University in the City of New York
C07K16/1063A61P31/18C07K2317/21C07K2317/31C07K2317/33C07K2317/52C07K2317/565C07K2317/567C07K2317/76C07K2317/92C07K2317/94
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,236,152
App. No.
15/772,443
Granted
Feb 1, 2022
Kind
B2
Abstract

Neutralizing antibodies that specifically bind to HIV-1 Env and antigen binding fragments of these antibodies are disclosed. Nucleic acids encoding these antibodies, vectors and host cells are also provided. Methods for detecting HIV-1 using these antibodies are disclosed. In addition, the use of these antibodies, antigen binding fragment, nucleic acids and vectors to prevent and/or treat an HIV-1 infection is disclosed.

Claims (34)

1. An isolated antibody, comprising:

a heavy chain variable region (V H ) comprising a heavy chain complementarity determining region (HCDR)1, a HCDR2, and a HCDR3 of the V H set forth as SEQ ID NO: 75, and a light chain variable region (V L ) comprising a light chain complementarity determining region (LCDR)1, a LCDR2, and a LCDR3 of the V L set forth as SEQ ID NO: 6, wherein the HCDR1, the HCDR2, the HCDR3, the LCDR1, the LCDR2, and the LCDR3 comprise the amino acid sequences set forth as: SEQ ID NOs: 7, 8, 77, 10, 11, and 12, respectively (10E8v4 S100cF CDRs); and

wherein the antibody specifically binds to gp41 and neutralizes HIV-1.

2. The isolated antibody of claim 1 , wherein

the V H comprises arginine, glutamate, serine, lysine, aspartate, threonine, lysine, threonine, valine, threonine, threonine, tyrosine, glutamine, and isoleucine residues at kabat positions 3, 61, 62, 64, 72, 74, 75, 77, 82c, 84, 87, 89, 105, and 110, respectively; and

the V L comprises alanine, serine, aspartate, proline, alanine, lysine, glutamine, valine, isoleucine, threonine, glutamate, and aspartate residues at kabat positions 1, 2, 7, 8, 9, 16, 17, 45, 58, 76, 83, and 85, respectively.

3. The isolated antibody of any of claim 1 , comprising an arginine residue at kabat position 5.

4. An isolated antibody, comprising:

a V H comprising a HCDR1, a HCDR2, and a HCDR3 of the V H set forth as SEQ ID NO: 75, and a light chain variable region (V L ) comprising a LCDR1, a LCDR2, and a LCDR3 of the V L set forth as SEQ ID NO: 6, wherein the HCDR1, the HCDR2, the HCDR3, the LCDR1, the LCDR2, and the LCDR3 comprise the amino acid sequences set forth as: SEQ ID NOs: 7, 8, 77, 10, 11, and 12, respectively (10E8v4 S100cF CDRs);

wherein the V H and the V L framework regions (FRs) further comprise amino acid sequences at least 90% identical to the V H and V L FRs of SEQ ID NOs: 75 and 6, respectively (10E8v4 S100cF); and

wherein the antibody specifically binds to gp41 and neutralizes HIV-1.

5. An isolated antibody, comprising:

a V H comprising a HCDR1, a HCDR2, and a HCDR3 of the V H set forth as SEQ ID NO: 75, and a light chain variable region (V L ) comprising a LCDR1, a LCDR2, and a LCDR3 of the V L set forth as SEQ ID NO: 6, wherein the HCDR1, the HCDR2, the HCDR3, the LCDR1, the LCDR2, and the LCDR3 comprise the amino acid sequences set forth as: SEQ ID NOs: 7, 8, 77, 10, 11, and 12, respectively (10E8v4 S100cF CDRs);

wherein the V H and the V L framework regions (FRs) further comprise amino acid sequences at least 90% identical to the V H and V L FRs of SEQ ID NOs: 76 and 6, respectively (10E8v4 V5R S100cF) and

wherein the antibody specifically binds to gp41 and neutralizes HIV-1.

6. The isolated antibody of claim 1 , wherein the V H and V L comprise the amino acid sequences set forth as SEQ ID NOs: 75 and 6, respectively (10E8v4 S100cF).

7. The isolated antibody of claim 1 , wherein the V H and V L comprise the amino acid sequences set forth as SEQ ID NOs: 76 and 6, respectively (10E8v4 V5R S100cF).

8. The isolated antibody of claim 1 , wherein the antibody dissolves to a concentration of at least 5 mg/ml in phosphate buffered saline, pH 7.4, at 20° C.

9. The isolated antibody of claim 1 , comprising human framework regions.

10. The isolated antibody of claim 1 , comprising a human constant region.

11. The isolated antibody of claim 1 , wherein the antibody is an IgG, IgM or IgA.

12. The isolated antibody of claim 1 , comprising a recombinant constant region comprising a modification that increases binding to the neonatal Fc receptor.

13. The isolated antibody of claim 12 , wherein the antibody is an IgG1 and the modification that increases binding to the neonatal Fc receptor comprises M428L and N434S amino acid substitutions.

14. An antigen binding fragment of the antibody of claim 1 .

15. The antigen binding fragment of claim 14 , wherein the antigen binding fragment is a Fv, Fab, F(ab′) 2 , scFV or a scFV 2 fragment.

16. The antibody of claim 1 , or an antigen binding fragment thereof, linked to an effector molecule or a detectable marker.

17. A method of detecting an HIV-1 infection in a subject, comprising:

contacting a biological sample from the subject with the antibody of claim 1 or an antigen binding fragment thereof under conditions sufficient to form an immune complex; and

detecting the presence of the immune complex on the sample, wherein the presence of the immune complex on the sample indicates that the subject has the HIV-1 infection.

18. A method of inhibiting or treating an HIV-1 infection in a subject, comprising administering to the subject a therapeutically effective amount of the antibody of claim 1 , or an antigen binding fragment thereof, thereby inhibiting or treating the HIV-1 infection.

19. The method of claim 18 , wherein the subject is at risk of an HIV-1 infection, has an HIV-1 infection, or has AIDS.

20. The method of claim 18 , further comprising administering to the subject an additional antibody that specifically binds to HIV-1 Env and neutralizes HIV-1 infection.

21. The method of claim 20 , wherein the additional antibody is a VRC01-class antibody.

22. The method of claim 21 , wherein the VRC01-class antibody is VRC01 or VRC07-523.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2021
From: SHAPIRO, LAWRENCE; GINDIN, TATYANA
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 058387/0018 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2021
From: KWONG, PETER; KWON, YOUNG DO; GEORGIEV, IVELIN; OFEK, GILAD; ZHANG, BAOSHAN; MCKEE, KRISHA; MASCOLA, JOHN; CHUANG, GWO-YU; O'DELL, SIJY; BAILER, ROBERT; LOUDER, MARK; ASOKAN, MANGAIARKARASI; SCHWARTZ, RICHARD; COOPER, JONATHAN; CARLTON, KEVIN; BENDER, MICHAEL; CONNORS, MARK; PEGU, AMARENDRA; KUELTZO, LISA
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 058964/0700 →
Continuity (2)
Provisional Application 62250360 · Nov 3, 2015
Related Publication 20190077849A1 · Mar 14, 2019