IP Library Granted Patent US 9,765,156
Granted Patent B2
US 9,765,156 · App. 14/410,427 · Granted Sep 19, 2017

Enhancing activity of CAR T cells by co-introducing a bispecific antibody

Inventors: Carl H. June (Merion Station, PA); Yangbing Zhao (Lumberton, NJ); Xiaojun Liu (Swarthmore, PA)
Assignee: The Trustees of the University of Pennsylvania
C07K16/468A61K35/17C07K16/2803C07K16/2809A61K47/48676A61K2039/505C07K2317/21C07K2317/24C07K2317/31C07K2317/622
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Quick Facts
Patent No.
US 9,765,156
App. No.
14/410,427
Granted
Sep 19, 2017
Kind
B2
Abstract

The present invention provides compositions and methods for treating cancer in a human. The invention includes administering a T cell, genetically modified to express a chimeric antigen receptor (CAR), a bispecific antibody, or a combination thereof to a subject. The CAR and bispecific antibody of the invention can comprise a human antibody, a humanized antibody, or antigen-binding fragments thereof.

Claims (12)

1. A method for stimulating a T cell-mediated immune response to a tumor cell population or tumor tissue in a mammal, the method comprising administering to the mammal an effective amount of a T cell, wherein the T cell is genetically modified to coexpress a CAR and a bispecific antibody, wherein the CAR comprises a tumor antigen binding domain, a transmembrane domain, and a CD3 zeta signaling domain, further wherein the tumor antigen binding domain is selected from the group consisting of a human antibody, a humanized antibody, and an antigen binding fragment thereof, thereby stimulating a T cell-mediated immune response to the tumor cell population or tumor tissue in the mammal, and wherein the bispecific antibody comprises a domain that binds a T cell antigen and does not comprise a transmembrane domain.

2. A method for stimulating a T cell-mediated immune response to a target tumor cell population or tumor tissue in a human, the method comprising administering to the human an effective amount of a T cell, wherein the T cell is genetically modified to express a CAR, and wherein the CAR comprises a polypeptide encoded by the nucleic acid sequence selected from the group consisting of SEQ ID NOs: 20, SEQ ID NO: 21, and SEQ ID NO: 22, thereby stimulating a T cell-mediated immune response to the target tumor cell population or tumor tissue in the human.

3. A method of treating a mammal with a tumor or cancer associated with an elevated expression of a tumor antigen, the method comprising administering to the mammal an effective amount of a T cell, wherein the T cell is genetically modified to coexpress a CAR and a bispecific antibody, wherein the CAR comprises a tumor antigen binding domain, a transmembrane domain, and a CD3 zeta signaling domain, further wherein the tumor antigen binding domain is selected from a human antibody, a humanized antibody, and an antigen binding fragment thereof, thereby treating the mammal, and wherein the bispecific antibody comprises a domain that binds a T cell antigen and does not comprise a transmembrane domain.

4. A method of treating a human with a tumor or cancer associated with an elevated expression of a tumor antigen, the method comprising administering to the human an effective amount of a T cell, wherein the T cell is genetically modified to express a CAR, and wherein the CAR comprises a polypeptide encoded by the nucleic acid sequence selected from the group consisting of SEQ ID NOs: 20, SEQ ID NO: 21, and SEQ ID NO: 22, thereby treating the human.

5. A method of treating a human with cancer, the method comprising administering to the human a T cell, wherein the T cell is genetically engineered to coexpress a CAR and a bispecific antibody, wherein the CAR comprises a tumor antigen binding domain, a transmembrane domain, and a CD3 zeta signaling domain, further wherein the tumor antigen binding domain is selected from a human antibody, a humanized antibody, and an antigen binding fragment thereof, and wherein the bispecific antibody comprises a domain that binds a T cell antigen and does not comprise a transmembrane domain.

6. A method of treating a human with cancer, the method comprising administering to the human a T cell, wherein the T cell is genetically engineered to express a CAR, and wherein the CAR comprises a polypeptide encoded by the nucleic acid sequence selected from the group consisting of SEQ ID NOs: 20, SEQ ID NO: 21, and SEQ ID NO: 22.

7. The method of claim 1 , wherein the bispecific antibody binds a tumor antigen.

8. The method of claim 3 , wherein the bispecific antibody binds a tumor antigen.

9. The method of claim 5 , wherein the bispecific antibody binds a tumor antigen.

10. The method of claim 1 , wherein the mammal is a human and the bispecific antibody comprises a polypeptide encoded by the nucleic acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, and SEQ ID NO: 19.

11. The method of claim 3 , wherein the mammal is a human and the bispecific antibody comprises a polypeptide encoded by the nucleic acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, and SEQ ID NO: 19.

12. The method of claim 5 , wherein the bispecific antibody comprises a polypeptide encoded by the nucleic acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, and SEQ ID NO: 19.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2017
From: JUNE, CARL H.; ZHAO, YANGBING; LIU, XIAOJUN
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 043769/0951 →
Continuity (2)
Provisional Application 61671535 · Jul 13, 2012
Related Publication 20150322169A1 · Nov 12, 2015