IP Library Granted Patent US 12,427,183
Granted Patent B2
US 12,427,183 · App. 17/523,261 · Granted Sep 30, 2025

Methods of treating cancer, infectious disease, and autoimmune disease using chemokines

Inventor: Franck Barrat (New York, NY)
Assignee: New York Society For The Relief Of The Ruptured And Crippled, The Hospital For Maintaining, Special Surgery
A61K38/195A61K45/06A61P35/00
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Quick Facts
Patent No.
US 12,427,183
App. No.
17/523,261
Granted
Sep 30, 2025
Kind
B2
Abstract

The current invention is related to the prevention and treatment of diseases including cancer, autoimmune disease, and infectious disease using chemokines and the receptors to which they agonize. It has been found that certain chemokines, including CXCL4, CXCL9, CXCL10, and CXCL12 as well as CCL5 have various effects on toll-like receptors in various cell types and these can be utilized for disease treatment and prevention.

Claims (14)

1. A method of activating an immune response in a subject having cancer, comprising administering to the subject a therapeutically effective amount of a chemokine selected from the group consisting of CXCL10, CXCL12 and CCL5, wherein the chemokine potentiates the response of toll-like receptor (TLR) 9 to produce interferon-α in plasmacytoid dendritic cells from the subject and the activation of the immune response is beneficial to treating cancer.

2. The method of claim 1 , wherein the cancer is chosen from the group consisting of lung cancer, colon cancer, melanoma, pancreatic cancer, mammary cancer, prostate cancer, breast cancer, ovarian cancer, basal cell carcinoma, biliary tract cancer, bladder cancer, bone cancer, cervical cancer, colon and rectum cancer, connective tissue cancer, cancer of the digestive system, endometrial cancer, esophageal cancer, cancer of the head and neck, kidney cancer, larynx cancer, liver cancer, fibroma, neuroblastoma, oral cavity cancer, skin cancer, testicular cancer, thyroid cancer, uterine cancer, medulloblastoma, sarcoma, squamous cell carcinoma, and lymphoma.

3. The method of claim 1 , wherein the chemokine is administered by injection directly into a tumor in the subject.

4. The method of claim 1 , further comprising administering to the subject an agonist of TLR9.

5. The method of claim 4 , wherein the agonist is chosen from the group consisting of CpG nucleotides, CpG-A, CpG-B and CpG-C.

6. The method of claim 4 , further comprising administering to the subject a checkpoint inhibitor.

7. The method of claim 6 , wherein the checkpoint inhibitor inhibits a protein selected from the group consisting of CTLA-4, PD-L1, PD-L2, and PD-1.

8. The method of claim 1 , wherein the chemokine is administered via the administration of plasmacytoid dendritic cells into tumor tissue in the subject, wherein the plasmacytoid dendritic cells have been contacted ex vivo with the chemokine peptide or protein and further contacted with an agonist of TLR9.

9. The method of claim 8 , wherein the plasmacytoid dendritic cells were obtained from the subject.

10. The method of claim 8 , wherein the TLR9 agonist is chosen from the group consisting of CpG nucleotides, CpG-A, CpG-B and CpG-C.

11. A method of increasing the effectiveness of an immunogenic composition comprising at least one CpG in protecting against an infectious disease in a subject comprising administering a therapeutically effective amount of a chemokine selected from the group consisting of CXCL10, CXCL12 and CCL5, wherein a therapeutically effective amount of the immunogenic composition comprising at least one CpG has been administered or will be administered to the subject and wherein the chemokine potentiates the response of toll-like receptor (TLR) 9 to produce interferon-α in plasmacytoid dendritic cells from the subject and the activation of the immune response increases the effectiveness of the immunogenic composition.

12. The method of claim 11 , wherein the infectious disease is chosen from the groups consisting of chickenpox, diphtheria, hepatitis A, hepatitis B, human papillomavirus, influenza, measles, tetanus toxoid, anthrax, leishmania, shingles, mumps, rubella, polio, rotavirus, whooping cough, meningitis and COVID 19 (SARS-CoV-2 virus).

13. A method of protecting a subject having cancer from an infectious disease comprising administering to the subject a therapeutically effective amount of a chemokine selected from the group consisting of CXCL10, CXCL12 and CCL5 and a therapeutically effective amount of an immunogenic composition comprising at least one CpG, wherein the chemokine potentiates the response of toll-like receptor (TLR) 9 to produce interferon-α in plasmacytoid dendritic cells from the subject and the activation of the immune response is beneficial to treating cancer.

14. The method of claim 13 , wherein the infectious disease is chosen from the group consisting of chickenpox, diphtheria, hepatitis A, hepatitis B, human papillomavirus, influenza, measles, tetanus toxoid, anthrax, leishmania, shingles, mumps, rubella, polio, rotavirus, whooping cough, meningitis and COVID 19 (SARS-CoV-2 virus).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 23, 2021
From: BARRAT, FRANCK
To: NEW YORK SOCIETY FOR THE RELIEF OF THE RUPTURED AND CRIPPLED, MAINTAINING THE HOSPITAL FOR SPECIAL SURGERY
Reel/Frame 058191/0980 →
Continuity (4)
Continuation In Part 15839105 · Dec 12, 2017
Provisional Application 62492562 · May 1, 2017
Provisional Application 62433038 · Dec 12, 2016
Related Publication 20220072100A1 · Mar 10, 2022
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