Method of promoting a t-cell response or treating cancer by administering an antagonist to human c-type lectin-like receptor-1 (CLEC-1)

Patent metadata

Field	Value
Publication number	US-12091464-B2
Application number	US-202217740849-A
Country	US
Kind code	B2
Filing date	May 10, 2022
Priority date	Oct 21, 2016
Publication date	Sep 17, 2024
Grant date	Sep 17, 2024

Abstract

The present invention relates to methods for promoting T cells response. The inventors examined the expression and function of CLEC-1 in human DCs and demonstrated for the first time a cell-surface expression. They investigated its functional role following triggering on orchestration of T-cell responses. The inventors showed in vitro and in vivo with CLEC-1 deficient rats and rat CLEC-1 Fc fusion protein that disruption of CLEC-1 signalling enhances in vitro Th17 activation and in vivo enhances T cell priming and Th17 and Th1 activation. In particular, the present invention relates to CLEC-1 antagonists for promoting T cells response in a subject in need thereof.

First claim

The invention claimed is:

1. A method of promoting a T-cell response in a human subject suffering from cancer comprising administering to the subject a therapeutically effective amount of an antagonist of human CLEC-1.

2. The method of claim 1 , wherein the human subject suffers from a cancer selected from the group consisting of bile duct cancer, bladder cancer, bone cancer, brain and central nervous system cancer, breast cancer, Castleman disease cervical cancer, colorectal cancer, endometrial cancer, esophagus cancer, gallbladder cancer, gastrointestinal carcinoid tumors, Hodgkin's disease, non-Hodgkin's lymphoma, Kaposi's sarcoma, kidney cancer, laryngeal and hypopharyngeal cancer, liver cancer, lung cancer, mesothelioma, plasmacytoma, nasal cavity and paranasal sinus cancer, nasopharyngeal cancer, neuroblastoma, oral cavity and oropharyngeal cancer, ovarian cancer, pancreatic cancer, penile cancer, pituitary cancer, prostate cancer, retinoblastoma, rhabdomyosarcoma, salivary gland cancer, skin cancer, stomach cancer, testicular cancer, thymus cancer, thyroid cancer, vaginal cancer, vulvar cancer, and uterine cancer.

3. The method according to claim 1 , wherein the antagonist of human CLEC-1 is an antibody or an antigen-binding fragment thereof.

4. The method of claim 3 , wherein the antagonist of human CLEC-1 is selected from the group consisting of chimeric antibodies, humanized antibodies and fully human monoclonal antibodies.

5. The method of claim 3 , wherein the antibody or antigen-binding fragment thereof specifically binds to the extracellular domain of human CLEC-1.

6. The method according to claim 1 , wherein the antagonist of human CLEC-1 is an aptamer.

7. A method of treating cancer, by promoting a T-cell response, in a human subject in need thereof comprising administering to the subject a therapeutically effective amount of an antagonist of human CLEC-1.

8. The method according to claim 7 , wherein the antagonist of human CLEC-1 is used in combination with a conventional treatment.

9. The method according to claim 8 , wherein the antagonist of human CLEC-1 is used in combination with a chemotherapeutic agent, a targeted cancer therapy, an immunotherapeutic agent or radiotherapy.

Assignees

• Inst Nat Sante Rech Med
• Univ Nantes
• Ose Immunotherapeutics

Inventors

• Chiffoleau Elise
• Teppaz Geraldine
• Poirier Nicolas
• Vanhove Bernard
• Gauttier Vanessa

Classifications

• C12N15/115

  Aptamers, i.e. nucleic acids binding a target molecule specifically and with high affinity without hybridising therewith {; Nucleic acids binding to non-nucleic acids, e.g. aptamers} · CPC title

• C07K2319/30

  Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto · CPC title

• C07K2317/76

  Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title

• C07K2317/732

  Antibody-dependent cellular cytotoxicity [ADCC] · CPC title

• C07K14/4726 Primary

  Lectins · CPC title