Anti-KIR3D antibodies

US9828427B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9828427-B2
Application numberUS-201514924786-A
CountryUS
Kind codeB2
Filing dateOct 28, 2015
Priority dateJan 19, 2009
Publication dateNov 28, 2017
Grant dateNov 28, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention provides antigen-binding proteins capable of binding to KIR3D polypeptides. The antibodies have increased activity in the treatment of disorders characterized by KIR3DL2-expressing cells, particularly CD4+ T cells, including malignancies such as Mycosis Fungoides and Sézary Syndrome.

First claim

Opening claim text (preview).

We claim: 1. A method of modulating T cell activity in a patient suffering from arthritis, rheumatoid arthritis, or spondylarthritis comprising the step of administering to said patient a composition comprising a pharmaceutically acceptable carrier or excipient and an antibody that specifically binds to an epitope within the KIR3DL2 domain 0 consisting of SEQ ID NO: 21, wherein said antibody inhibits proliferation of KIR3DL-expressing human T lymphocytes and comprises a constant region of human IgG isotype, wherein said antibody: (a) comprises an Fc region of an IgG isotype modified to decrease binding to Fc receptors; and/or (b) does not substantially induce ADCC of a KIR3DL-expressing target cell. 2. The method of claim 1 , further comprising administering to the patient an immune system suppressor. 3. The method of claim 1 , wherein said patient suffers from arthritis. 4. The method of claim 1 , wherein said patient suffers from rheumatoid arthritis. 5. The method of claim 1 , wherein said patient suffers from spondylarthritis. 6. The method of claim 1 , wherein said antibody does not substantially induce ADCC of a KIR3DL-expressing target cell. 7. The method of claim 1 , wherein said antibody comprises an Fc region of an IgG isotype modified to decrease binding to Fc receptors.

Assignees

Inventors

Classifications

  • Immunosuppressants, e.g. drugs for graft rejection · CPC title

  • specific for metastasis · CPC title

  • Immunomodulators · CPC title

  • Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title

  • Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9828427B2 cover?
The present invention provides antigen-binding proteins capable of binding to KIR3D polypeptides. The antibodies have increased activity in the treatment of disorders characterized by KIR3DL2-expressing cells, particularly CD4+ T cells, including malignancies such as Mycosis Fungoides and Sézary Syndrome.
Who is the assignee on this patent?
Innate Pharma
What technology area does this patent fall under?
Primary CPC classification C07K16/2803. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).