IP Library Granted Patent US 10,316,093
Granted Patent B2
US 10,316,093 · App. 15/505,872 · Granted Jun 11, 2019

Antibodies, compositions, and uses

Inventors: Nai-Kong V. Cheung (New York, NY); Mahiuddin Ahmed (Verona, NJ); Qi Zhao (Tseung Kwan, HK)
Assignee: MEMORIAL SLOAN KETTERING CANCER CENTER
C07K16/2827A61K35/17A61K51/1027C07K16/2809C07K16/32C12N15/85A61K2039/505A61K2039/53A61K2039/552C07K2299/00C07K2317/24C07K2317/31C07K2317/51C07K2317/515C07K2317/55C07K2317/56C07K2317/565C07K2317/567C07K2317/622C07K2317/732C07K2317/76C07K2317/92C07K2317/94
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 10,316,093
App. No.
15/505,872
Granted
Jun 11, 2019
Kind
B2
Abstract

The present disclosure describes anti-B7H3 antibody agents and uses relating thereto. Among other things, the present disclosure demonstrates particular immunomodulatory effectiveness of certain such antibodies. The present disclosure further describes particularly high-affinity or otherwise useful antibodies and antibody agents based thereon, including particularly certain humanized and/or affinity matured versions of an 8H9 antibody. In some embodiments, provided antibody agents are useful, for example, in the treatment of cancer. In some embodiments, provided antibody agents are useful in relieving immunosuppression, for example mediated by B7H3-positive cells.

Claims (41)

1. An antibody agent comprising an immunoglobulin heavy chain and an immunoglobulin light chain, wherein the antibody agent binds specifically to protein 2Ig-B7H3 or 4Ig-B7H3, and wherein said immunoglobulin light chain comprises a sequence as set forth in a SEQ ID NO. selected from the group consisting of SEQ ID NO.: 1, 2, 3, 4, 5, 6, 7 and 8, and said immunoglobulin heavy chain comprises a sequence as set forth in a SEQ ID NO. selected from the group consisting of SEQ ID NO.: 9, 10, 11, 12, 13, 14, 15 and 16.

2. The antibody agent of claim 1 , wherein:

(i) the immunoglobulin light chain is set forth in SEQ ID NO.: 1 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 9;

(ii) the immunoglobulin light chain is set forth in SEQ ID NO.: 2 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 10;

(iii) the immunoglobulin light chain is set forth in SEQ ID NO.: 3 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 11;

(iv) the immunoglobulin light chain is set forth in SEQ ID NO.: 4 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 12;

(v) the immunoglobulin light chain is set forth in SEQ ID NO.: 2 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 11;

(vi) the immunoglobulin light chain is set forth in SEQ ID NO.: 3 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 10;

(vii) the immunoglobulin light chain is set forth in SEQ ID NO.: 5 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 13;

(viii) the immunoglobulin light chain is set forth in SEQ ID NO.: 6 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 14;

(ix) the immunoglobulin light chain is set forth in SEQ ID NO.: 7 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 15; or

(x) the immunoglobulin light chain is set forth in SEQ ID NO.: 8 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 16.

3. The antibody agent of claim 1 , wherein the immunoglobulin light chain is set forth in SEQ ID NO.: 5 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 13.

4. The antibody agent of claim 1 , wherein the immunoglobulin light chain is set forth in SEQ ID NO.: 7 and the immunoglobulin heavy chain is set forth in SEQ ID NO.: 15.

5. The antibody agent of claim 1 , wherein the immunoglobulin light chain is fused to a polypeptide set forth in SEQ ID NO.: 30 or SEQ ID NO.: 31.

6. The antibody agent of claim 1 , conjugated to a therapeutic agent or detection agent.

7. The antibody agent of claim 6 , wherein the antibody is conjugated to a radio-isotope, a drug agent, a nanoparticle, or an immune-toxin.

8. The antibody agent of claim 6 , wherein the antibody is conjugated to a diagnostic or imaging agent, or both.

9. The antibody agent of claim 1 , wherein the antibody agent is a bispecific antibody.

10. The antibody agent of claim 9 , having a first and a second specificity, and wherein the first specificity binds to protein 2Ig-B7H3 or 4Ig-B7H3, and the second specificity binds to CD3 on T cells or 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA).

11. An scFv that binds specifically to protein 2Ig-B7H3 or 4Ig-B7H3 and comprising the polypeptide set forth in a SEQ ID NO. selected from the group consisting of SEQ ID NO.: 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 and 27.

12. The scFv of claim 11 , wherein the polypeptide is fused to a second polypeptide set forth in SEQ ID NO.: 28 or SEQ ID NO.: 29.

13. The scFv of claim 11 , wherein the scFv is conjugated to a therapeutic agent or detection agent.

14. A pharmaceutical composition comprising the antibody agent of claim 1 and a pharmaceutically acceptable carrier.

15. A method of treating cancer, comprising administering to a patient in need thereof a therapeutically effective amount of the antibody agent of claim 1 .

16. A method of modulating the immune system, comprising administering to a patient in need thereof a therapeutically effective amount of the antibody agent of claim 1 .

17. The method of claim 15 , wherein the cancer is or comprises a neuroblastoma.

18. The method of claim 15 , wherein the cancer is or comprises a cervical cancer.

19. The method of claim 15 , wherein the cancer comprises B7H3-positive tumor cells.

20. A method of enhancing T-cell mediated cytotoxicity in a subject, the method comprising steps of:

administering to a subject a composition comprising an antibody agent that binds to B7H3's FG-loop, wherein the antibody agent comprises:

(i) light chain CDR1, CDR2, and CDR3 as set forth in SEQ ID NOs: 34, 36, and 38, respectively, and heavy chain CDR1, CDR2, and CDR3 as set forth in 58, 60, and 62, respectively;

(ii) light chain CDR1, CDR2, and CDR3 as set forth in SEQ ID NOs: 40, 42, and 44, respectively, and heavy chain CDR1, CDR2, and CDR3 as set forth in 64, 66, and 68, respectively;

(iii) light chain CDR1, CDR2, and CDR3 as set forth in SEQ ID NOs: 46, 48, and 50, respectively, and heavy chain CDR1, CDR2, and CDR3 as set forth in 70, 72, and 74, respectively; or

(iv) light chain CDR1, CDR2, and CDR3 as set forth in SEQ ID NOs: 52, 54, and 56, respectively, and heavy chain CDR1, CDR2, and CDR3 as set forth in 76, 78, and 80, respectively.

21. The method of claim 20 , wherein the antibody agent comprises an immunoglobulin heavy chain and an immunoglobulin light chain, wherein said immunoglobulin heavy chain comprises a sequence as set forth in SEQ ID NO: 13 or 15, and said immunoglobulin light chain comprises a sequence as set forth in SEQ ID NO: 5 or 7.

22. A DNA or RNA encoding an antibody agent claim 1 .

23. A cell that expresses an antibody agent of claim 1 .

24. A method of preparing a cell that expresses an antibody agent, comprising transfecting or virally transducing a cell with the DNA of claim 22 .

25. A method of treating a patient by compartmental radioimmunotherapy (cRIT), comprising administering an antibody agent of claim 1 to a patient in need thereof.

26. The method of claim 25 , wherein the antibody is administered intrathecally, intraperitoneally, or by convection enhanced delivery.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2017
From: CHEUNG, NAI-KONG V.; AHMED, MAHIUDDIN; ZHAO, QI
To: MEMORIAL SLOAN KETTERING CANCER CENTER
Reel/Frame 041614/0319 →
Continuity (2)
Provisional Application 62042457 · Aug 27, 2014
Related Publication 20170240637A1 · Aug 24, 2017
Cited By (1)
US 12,565,529