IP Library Granted Patent US 9,205,153
Granted Patent B2
US 9,205,153 · App. 14/049,563 · Granted Dec 8, 2015

Immune modulation via C-type lectin

Inventors: David Sancho-Madrid (London, GB); Oliver Schulz (London, GB); Neil Charles Rogers (London, GB); Caetano Reis e Sousa (London, GB); Olivier Pierre Joffre (London, GB); Daniel Pennington (London, GB)
Assignee: Cancer Research Technology Limited
A61K47/48415A61K39/0005A61K39/0011C07K16/2851C07K16/2878A61K2039/507A61K2039/57A61K2039/6056C07K2316/96C07K2317/55C07K2317/75C07K2319/33
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Quick Facts
Patent No.
US 9,205,153
App. No.
14/049,563
Granted
Dec 8, 2015
Kind
B2
Abstract

The invention relates to the regulation of the immune system, and in particular to the finding that the CLEC9a molecule is a marker for dendritic cells which are capable of cross-presenting extracellular antigens via the MHC class I pathway. This makes them particularly suitable for generation of cytotoxic T lymphocyte responses. Materials and methods are provided both for the induction of immune responses against target antigens, and for the inhibition or suppression of undesirable immune responses in which these cells are involved.

Claims (9)

1. A composition comprising a peptide antigen, wherein the antigen is associated with a binding agent which comprises an antibody or functional fragment thereof having specific affinity for a CLEC9a protein of SEQ ID NO: 2 or SEQ ID NO:4, and wherein said antigen is a tumor-specific antigen or a human self antigen against which an immune response occurs in an auto-immune disease.

2. A composition according to claim 1 wherein said antibody or functional fragment has specific affinity for an extracellular domain of CLEC9a and said composition comprises a pharmaceutically acceptable carrier.

3. A composition according to claim 1 formulated for intravenous, intramuscular, intraperitoneal, nasal, subcutaneous or intradermal administration.

4. A composition according to claim 1 wherein the composition further comprises an adjuvant.

5. A composition according to claim 4 wherein the adjuvant is selected from the group consisting of retinoic acid, a CD40 agonist, a TLR agonist, and other immunostimulatory agents.

6. A composition according to claim 1 wherein the antigen is covalently coupled to the binding agent.

7. A composition according to claim 1 wherein the antigen and binding agent are part of the same peptide chain.

8. A composition according to claim 1 wherein the binding agent is an agonist of CLEC9a.

9. A composition according to claim 1 wherein the antigen is a tumour-specific antigen.

Priority Claims (1)
GB 0805159.1 · Mar 19, 2008 · national
Continuity (3)
Continuation 12669940
Provisional Application 60929999 · Jul 20, 2007
Related Publication 20140328865A1 · Nov 6, 2014