IP Library Granted Patent US 10,166,273
Granted Patent B2
US 10,166,273 · App. 15/501,028 · Granted Jan 1, 2019

Synergistic tumor treatment with antibodies targeting PD-1, PD-L1 or CTLA4 and integrin-binding-Fc-fusion protein

Inventors: Karl Dane Wittrup (Chestnut Hill, MA); Jennifer R. Cochran (Stanford, CA); Byron Hua Kwan (Boston, MA)
Assignee: The Board of Trustees of the Leland Stanford Junior University
A61K38/2013A61K38/16A61K38/179A61K38/385A61K39/39558A61K45/06A61K47/48215C07K14/55C07K16/22C07K16/249C07K16/28C07K16/2803C07K16/2812C07K16/2815C07K16/2818C07K16/30C07K16/3053C07K16/40A61K2039/505A61K2039/507C07K2317/52C07K2317/71C07K2317/76C07K2319/30C07K2319/31C07K2319/70
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Quick Facts
Patent No.
US 10,166,273
App. No.
15/501,028
Granted
Jan 1, 2019
Kind
B2
Abstract

The present invention provides a method of treating cancer with a combination of IL-2 and an integrin-binding-Fc fusion protein. The methods of the invention can be applied to a broad range of cancer types.

Claims (20)

1. A method for inhibiting growth and/or proliferation of tumor cells in a subject comprising administering to the subject an effective amount of an integrin-binding-Fc fusion protein, wherein the integrin-binding-Fc fusion protein comprises (i) an integrin-binding polypeptide comprising an integrin-binding loop and a knottin polypeptide scaffold; and (ii) an immunoglobulin Fc domain, wherein the integrin-binding polypeptide is operably linked to the Fc domain, and an immune checkpoint blocker selected from the group consisting of an antibody or antibody fragment targeting PD-1, an antibody or antibody fragment targeting PD-L1, and an antibody or antibody fragment targeting CTLA4.

2. The method of claim 1 , wherein the immune checkpoint blocker is an antibody or antibody fragment targeting PD-1.

3. The method of claim 1 , wherein the immune checkpoint blocker is an antibody or antibody fragment targeting CTLA4.

4. The method of claim 1 , wherein the integrin-binding polypeptide binds to a tumor-associated integrin selected from the group consisting of: αvβ3, αvβ5, α5β1, and any combination thereof.

5. The method of claim 1 , wherein the integrin-binding polypeptide binds to αvβ3, αvβ5, and α5β1.

6. The method of claim 1 , wherein the knottin polypeptide scaffold comprises at least three cysteine disulfide linkages or crosslinked cysteine residues, and wherein the integrin-binding loop is adjacent to cysteine residues of the knottin polypeptide scaffold.

7. The method of claim 6 , wherein the integrin-binding loop comprises an RGD peptide sequence.

8. The method of claim 6 , wherein the knottin polypeptide scaffold is derived from a knottin protein selected from the group consisting of: EETI-II, AgRP, and agatoxin.

9. The method of claim 8 , wherein the knottin protein is EETI-II.

10. The method of claim 1 , wherein the integrin-binding loop comprises an RGD peptide sequence and the knottin polypeptide scaffold is derived from EETI-II.

11. The method of claim 1 , wherein the integrin-binding polypeptide comprises the amino acid sequence set forth in SEQ ID NO: 42 or 43, wherein X 1 is selected from the group consisting of A, V, L, P, F, Y, S, H, D, and N; X 2 is selected from the group consisting of G, V, L, P, R, E, and Q; X 3 is selected from the group consisting of G, A, and P; X 7 is selected from the group consisting of W and N; X 8 is selected from the group consisting of A, P, and S; X 9 is selected from the group consisting of P and R; X 10 is selected from the group consisting of A, V, L, P, S, T, and E; and X 11 is selected from the group consisting of G, A, W, S, T, K, and E.

12. The method of claim 1 , wherein the integrin-binding polypeptide comprises the amino acid sequence set forth in any one of SEQ ID NOs: 67-133.

13. The method of claim 1 , wherein the integrin-binding polypeptide comprises the amino acid sequence set forth in SEQ ID NO: 94 or 96.

14. The method of claim 1 , wherein the Fc domain is a human IgG1 Fc domain.

15. The method of claim 1 , wherein the integrin-binding polypeptide is operably linked with or without a linker to the Fc domain.

16. The method of claim 1 , wherein the integrin-binding polypeptide is operably linked to the N-terminus of the Fc domain.

17. The method of claim 1 , wherein the integrin-binding polypeptide is operably linked to the C-terminus of the Fc domain.

18. The method of claim 1 , wherein the integrin-binding-Fc fusion protein comprises the amino acid sequence of SEQ ID NO: 48, 49, 50, or 51.

19. The method of claim 1 , further comprising administering an effective amount of an extended pharmacokinetic interleukin (IL)-2.

20. The method of claim 1 , wherein the immune checkpoint blocker is an antibody or antibody fragment targeting PD-L1.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2017
From: WITTRUP, KARL DANE; KWAN, BYRON HUA
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 042570/0970 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2017
From: COCHRAN, JENNIFER R.
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 042570/0974 →
CONFIRMATORY LICENSE Recorded Mar 24, 2017
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042086/0763 →
Continuity (2)
Provisional Application 62036554 · Aug 12, 2014
Related Publication 20170216402A1 · Aug 3, 2017
Cited By (1)
US 50,550