IP Library Granted Patent US 11,279,765
Granted Patent B2
US 11,279,765 · App. 16/628,941 · Granted Mar 22, 2022

Compositions and methods to improve anti-angiogenic therapy and immunotherapy

Inventors: Dai Fukumura (Newton, MA); Keehoon Jung (Boston, MA); Rakesh K. Jain (Wellesley, MA)
Assignee: The General Hospital Corporation
C07K16/2866A61K9/5123A61K31/713A61K47/62A61K47/6935A61P35/00C07K16/24C12N15/1136A61K9/0019A61K2039/505
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 11,279,765
App. No.
16/628,941
Granted
Mar 22, 2022
Kind
B2
Abstract

Agents that inhibit CX3CL1 in endothelial cells to reduce or inhibit immunosuppression mechanisms that are co-opted by cancer cells to evade host immune system, and that reduce immunosuppression in context of therapies that target VEGF-dependent signaling, and methods of use thereof.

Claims (16)

1. A composition comprising one or more inhibitory nucleic acids that comprises a siRNA or a locked nucleic acid (LNA) that bind to and reduce expression or activity of C-X3-C chemokine ligand 1 (CX3CL1), encapsulated within or linked to an endothelial cell delivery vehicle that comprises a lipid nanoparticle that comprises 7C1 nanoparticles, SAINT-C 18 lipoplexes, PEGylated SAINT-C18 lipoplexes, polyethyleneimine (PEI) PEGylated with an Arg-Gly-Asp (RGD) peptide (RGD-PEG-PEI) (RPP-nanoplexes), or Polycation Liposome-encapsulated Calcium Phosphate nanoparticles (PLCP).

2. The composition of claim 1 , wherein the siRNA is chemically modified to have increased siRNA half-life.

3. The composition of claim 1 , wherein the one or more inhibitory nucleic acids are linked to a cell-penetrating peptide.

4. A pharmaceutical composition comprising the composition of claim 1 , and a pharmaceutically acceptable carrier.

5. The pharmaceutical composition of claim 4 , further comprising an anti-angiogenic agent.

6. The pharmaceutical composition of claim 5 , wherein the anti-angiogenic agent is a VEGF inhibitor.

7. A method of treating a solid cancer, the method comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 4 .

8. The method of claim 7 , further comprising administering a therapeutically effective amount of an anti-angiogenic agent to the subject.

9. The method of claim 7 , wherein the subject has been treated with an anti-angiogenic agent prior to administration of the pharmaceutical composition of claim 4 .

10. The method of claim 8 , wherein the cancer is resistant to the anti-angiogenic.

11. The method of claim 8 , wherein the anti-angiogenic agent is a VEGF inhibitor.

12. The method of claim 8 , wherein the anti-angiogenic agent is administered prior to or concurrently with the pharmaceutical composition.

13. The method of claim 7 , wherein the cancer is a carcinoma.

14. The method of claim 13 , wherein the carcinoma is a colorectal, breast, or lung carcinoma.

15. The method of claim 7 , wherein the cancer is colorectal carcinoma.

16. The composition of claim 1 , wherein the endothelial cell delivery vehicle comprises 7C1 nanoparticles.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2020
From: FUKUMURA, DAI; JUNG, KEEHOON; JAIN, RAKESH K.
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 054782/0444 →
Continuity (2)
Provisional Application 62530124 · Jul 8, 2017
Related Publication 20200216549A1 · Jul 9, 2020