IP Library Granted Patent US 10,716,811
Granted Patent B2
US 10,716,811 · App. 16/207,568 · Granted Jul 21, 2020

Compositions and methods related to multimodal therapeutic cancer indications

Inventors: Avak Kahvejian (Lexington, MA); Jordi Mata-Fink (Somerville, MA); Robert J. Deans (Riverside, CA); Tiffany F. Chen (Cambridge, MA); John Round (Cambridge, MA); Noubar B. Afeyan (Lexington, MA); Torben Straight Nissen (Chestnut Hill, MA); Nathan Dowden (Winchester, MA); Tom Wickham (Groton, MA); Sivan Elloul (Newton, MA)
Assignee: Rubius Therapeutics Inc.
A61K35/18A61K35/12A61K38/191A61K39/0011A61K39/3955A61P17/00C07K14/705C12N5/0641A61K2039/505A61K2039/515C07K2319/00C12N2510/00
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Quick Facts
Patent No.
US 10,716,811
App. No.
16/207,568
Granted
Jul 21, 2020
Kind
B2
Abstract

The invention includes compositions and methods related to multimodal therapies, e.g., for treating a cancer. A multimodal therapy described herein provides and/or administers a plurality of agents that function in a coordinated manner to provide a therapeutic benefit to a subject in need thereof, e.g., a subject having a cancer.

Claims (22)

1. An enucleated erythroid cell comprising an exogenous polypeptide that comprises IL-12, or a receptor-binding fragment thereof, at the surface of the enucleated erythroid cell, wherein the exogenous polypeptide does not comprise a sortase transfer signature.

2. The enucleated erythroid cell of claim 1 , wherein the exogenous polypeptide comprises a transmembrane domain.

3. The enucleated erythroid cell of claim 1 , which is a reticulocyte.

4. The enucleated erythroid cell of claim 1 , which is an erythrocyte.

5. The enucleated erythroid cell of claim 1 , wherein the enucleated erythroid cell exhibits substantially the same osmotic membrane fragility as a corresponding isolated, unmodified, uncultured erythroid cell.

6. A pharmaceutical composition comprising (i) a plurality of the enucleated erythroid cells of claim 1 , wherein at least 70% of cells in the pharmaceutical composition are enucleated, and (ii) a pharmaceutically acceptable carrier.

7. The pharmaceutical composition of claim 6 , wherein at least 70% of enucleated erythroid cells in the pharmaceutical composition comprise the exogenous polypeptide.

8. The pharmaceutical composition of claim 6 , which comprises about 1×10 9 -1×10 13 cells.

9. A method of treating cancer in a subject, comprising administering to the subject a pharmaceutical composition of claim 6 , in an amount effective to treat cancer in the subject.

10. The method of claim 9 , wherein the cancer is a leukemia, a lymphoma, or a solid tumor.

11. The method of claim 9 , further comprising administering an anti-neoplastic drug to the subject.

12. The method of claim 9 , wherein the anti-neoplastic drug is a chemotherapeutic drug, a cancer growth blocker, a cancer vaccine, or a hormone therapy.

13. A method of making an enucleated erythroid cell of claim 1 , comprising:

introducing a nucleic acid encoding the exogenous polypeptide into a nucleated erythroid cell, or a precursor thereof; and

culturing the nucleated erythroid cell under conditions suitable for enucleation of the nucleated erythroid cell and for production of the exogenous polypeptide, thereby making the enucleated erythroid cell.

14. The method of claim 13 , which comprises expanding the nucleated erythroid cell, or precursor thereof, at least 1000-fold.

15. The enucleated erythroid cell of claim 1 , wherein the enucleated erythroid cell was produced by a process comprising introducing a nucleic acid encoding the exogenous polypeptide into a nucleated erythroid cell, or a precursor thereof.

16. The enucleated erythroid cell of claim 15 , wherein the process further comprises allowing enucleation to occur.

17. The enucleated erythroid cell of claim 15 , wherein the nucleic acid encoding the exogenous polypeptide is introduced using a lentivirus.

18. The enucleated erythroid cell of claim 2 , wherein the transmembrane domain comprises a glycophorin A (GPA) transmembrane domain.

19. The enucleated erythroid cell of claim 1 , wherein the exogenous polypeptide is a single fusion polypeptide comprising IL-12, or a receptor-binding fragment thereof.

20. The method of claim 9 , wherein the cancer is acute myeloid leukemia, cervical cancer, and head and neck cancer.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2019
From: KAHVEJIAN, AVAK; MATA-FINK, JORDI; ROUND, JOHN; AFEYAN, NOUBAR B.
To: FLAGSHIP PIONEERING, INC.
Reel/Frame 050929/0636 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2019
From: DEANS, ROBERT J.; CHEN, TIFFANY F.; STRAIGHT NISSEN, TORBEN; DOWDEN, NATHAN; WICKHAM, TOM; ELLOUL, SIVAN
To: RUBIUS THERAPEUTICS, INC.
Reel/Frame 050929/0663 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2019
From: FLAGSHIP PIONEERING, INC.
To: RUBIUS THERAPEUTICS, INC.
Reel/Frame 050929/0677 →
Continuity (7)
Continuation 15716141 · Sep 26, 2017
Continuation PCTUS2017013035 · Jan 11, 2017
Provisional Application 62420973 · Nov 11, 2016
Provisional Application 62370915 · Aug 4, 2016
Provisional Application 62359448 · Jul 7, 2016
Provisional Application 62277130 · Jan 11, 2016
Related Publication 20190083540A1 · Mar 21, 2019