IP Library Granted Patent US 11,274,298
Granted Patent B2
US 11,274,298 · App. 16/559,122 · Granted Mar 15, 2022

RNA engineered T cells for the treatment of cancer

Inventors: Carl H. June (Merion Station, PA); Yangbing Zhao (Lumberton, NJ)
Assignee: The Trustees of the University of Pennsylvania
C12N15/11A61K35/17A61K45/06C07K14/82A61K48/00C07K2319/03C07K2319/72C12N2799/027
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Quick Facts
Patent No.
US 11,274,298
App. No.
16/559,122
Granted
Mar 15, 2022
Kind
B2
Abstract

The present invention relates to compositions and methods for generating RNA Chimeric Antigen Receptor (CAR) transfected T cells. The RNA-engineered T cells can be used in adoptive therapy to treat cancer.

Claims (17)

1. An in vitro transcribed RNA or synthetic RNA, comprising a nucleic acid sequence encoding an extracellular domain, a transmembrane domain, a costimulatory signaling region, and a signaling domain of CD3-zeta, wherein the RNA is transcribed from an in vitro transcription vector or a DNA,

wherein the in vitro transcription vector comprises the nucleic acid sequence of SEQ ID NO: 4, 5, 27, or 28, and

wherein the DNA comprises the nucleic acid sequence of any one of SEQ ID NOs: 6-24.

2. The RNA of claim 1 , wherein the extracellular domain comprises an antigen binding moiety.

3. The RNA of claim 2 , wherein the antigen binding moiety binds to a tumor antigen.

4. The RNA of claim 3 , wherein the tumor antigen is an antigen associated with a cancer selected from the group consisting of brain cancer, bladder cancer, breast cancer, cervical cancer, colorectal cancer, liver cancer, kidney cancer, lymphoma, leukemia, lung cancer, melanoma, metastatic melanoma, mesothelioma, neuroblastoma, ovarian cancer, prostate cancer, pancreatic cancer, renal cancer, skin cancer, thymoma, sarcoma, non-Hodgkin's lymphoma, Hodgkin's lymphoma, uterine cancer, and any combination thereof.

5. The RNA of claim 1 , wherein the vector comprises the nucleic acid sequence of SEQ ID NO: 4.

6. The RNA of claim 1 , wherein the DNA comprises the nucleic acid sequence of SEQ ID NO: 6 or 8.

7. The RNA of claim 1 , wherein the vector comprises the nucleic acid sequence of SEQ ID NO: 5.

8. The RNA of claim 1 , wherein the DNA comprises a sequence selected from the group consisting of SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23 and SEQ ID NO: 24.

9. The RNA of claim 1 , wherein the vector comprises the nucleic acid sequence of SEQ ID NO: 28.

10. The RNA of claim 1 , wherein the DNA comprises a sequence selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13.

11. The RNA of claim 1 , wherein the vector comprises the nucleic acid sequence of SEQ ID NO: 27.

12. The RNA of claim 1 , wherein the DNA comprises a sequence selected from the group consisting of SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17 and SEQ ID NO: 18.

13. The RNA of claim 1 , wherein the costimulatory signaling region comprises the intracellular domain of a costimulatory molecule selected from the group consisting of CD27, CD28, 4-1BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, a ligand that specifically binds with CD83, and any combination thereof.

14. The RNA of claim 1 , wherein the nucleic acid sequence comprises a poly(A) tail comprising about 150 adenosine bases.

15. The RNA of claim 1 , wherein the nucleic acid sequence comprises a 3′UTR comprising at least one repeat of a 3′UTR derived from human beta-globin.

Continuity (3)
Division 14342904
Provisional Application 61535608 · Sep 16, 2011
Related Publication 20200087659A1 · Mar 19, 2020