Methods of obtaining a specific binding member that binds eotaxin

US9284589B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9284589-B2
Application numberUS-201414223561-A
CountryUS
Kind codeB2
Filing dateMar 24, 2014
Priority dateMar 3, 2000
Publication dateMar 15, 2016
Grant dateMar 15, 2016

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.

Specific binding members directed to eotaxin-1, in particular human antibodies and antibody fragments against human eotaxin-1 and especially those which neutralize eotaxin-1 activity. The antibodies VH and/or VL domain of the scFv fragment herein termed CAT-212 and of the IgG4 antibody herein termed CAT 213. One or more complementary determining regions (CDRs) of the CAT-212/-213 VH and/or VL domains, especially VH CRD3 in other antibody framework regions. Compositions containing specific binding members, and their use in methods of inhibiting or neutralizing eotaxin, including methods of treatment of the human or animal body by therapy.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method of producing an antibody heavy chain variable region (VH) domain, the method comprising culturing host cells under conditions for production of said VH domain, wherein said host cells are transformed with a nucleic acid which comprises a nucleotide sequence encoding a polypeptide comprising a VH domain, wherein said VH domain comprises VH CDRs 1-3 with the amino acid sequences of SEQ ID NO:5, SEQ ID NO:6 and SEQ ID NO:7, respectively, and wherein when the VH domain is paired with an antibody light chain variable region (VL) domain comprising VL CDRs 1-3 with the amino acid sequences of SEQ ID NO:8, SEQ ID NO:9 and SEQ ID NO:10, respectively, an antibody antigen binding site that binds eotaxin is provided. 2. The method according to claim 1 , wherein said VH domain comprises the CAT-212 VH domain (SEQ ID NO:2). 3. The method according to claim 1 , further comprising isolating and/or purifying said VH domain. 4. The method according to claim 1 , further comprising formulating the VH domain into a composition including at least one additional component. 5. The method of claim 1 , wherein the polypeptide further comprises an antibody heavy chain constant region. 6. The method of claim 5 , wherein the antibody heavy chain constant region is an IgG4 constant region. 7. A method of producing an antibody light chain variable region (VL) domain, the method comprising culturing host cells under conditions for production of said VL domain, wherein said host cells are transformed with a nucleic acid which comprises a nucleotide sequence encoding a polypeptide comprising a VL domain, wherein said VL domain comprises VL CDRs 1-3 with the amino acid sequences of SEQ ID NO:8, SEQ ID NO:9 and SEQ ID NO:10, respectively, and wherein when the VL domain is paired with an antibody heavy chain variable region (VH) domain comprising VH CDRs 1-3 with the amino acid sequences of SEQ ID NO:5, SEQ ID NO:6 and SEQ ID NO:7, respectively, an antibody antigen binding site that binds eotaxin is provided. 8. The method according to claim 7 , wherein said VL domain comprises the CAT-212 VL domain (SEQ ID NO:4). 9. The method according to claim 7 , further comprising isolating and/or purifying said VL domain. 10. The method according to claim 7 , further comprising formulating the VL domain into a composition including at least one additional component. 11. The method of claim 7 , wherein the polypeptide further comprises an antibody light chain constant region. 12. The method of claim 11 , wherein the antibody light chain constant region is a Cλ constant region.

Assignees

Inventors

Classifications

  • Antiallergic agents (antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14) · CPC title

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

  • Ophthalmic agents · CPC title

  • Drugs for dermatological disorders · CPC title

  • for treating wounds, ulcers, burns, scars, keloids, or the like · 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 US9284589B2 cover?
Specific binding members directed to eotaxin-1, in particular human antibodies and antibody fragments against human eotaxin-1 and especially those which neutralize eotaxin-1 activity. The antibodies VH and/or VL domain of the scFv fragment herein termed CAT-212 and of the IgG4 antibody herein termed CAT 213. One or more complementary determining regions (CDRs) of the CAT-212/-213 VH and/or VL d…
Who is the assignee on this patent?
Medimmune Ltd
What technology area does this patent fall under?
Primary CPC classification C07K16/24. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 15 2016 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).