Humanized antibodies with increased stability
US-2019276536-A1 · Sep 12, 2019 · US
US10577419B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10577419-B2 |
| Application number | US-201514662349-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 19, 2015 |
| Priority date | Sep 19, 2012 |
| Publication date | Mar 3, 2020 |
| Grant date | Mar 3, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to methods for the treatment of cancer and inflammatory disease using antibodies (e.g. monoclonal antibodies), antibody fragments, and derivatives thereof that specifically bind KIR3DL2. The invention also relates to antibodies, cells producing such antibodies; methods of making such antibodies; fragments, variants, and derivatives of the antibodies; pharmaceutical compositions comprising the same.
Opening claim text (preview).
We claim: 1. A monoclonal antibody that binds a KIR3DL2 polypeptide comprising SEQ ID NO: 1, wherein said antibody does not substantially bind to a KIR3DL1 polypeptide comprising SEQ ID NO: 169, and wherein said antibody is not internalized into KIR3DL2-expressing cells, wherein said antibody has (i) a heavy chain comprising CDRs 1, 2 and 3 (HCDR1, HCDR2, HCDR3), according to the Kabat definition, of the heavy chain variable region sequence of SEQ ID NO: 13, and (ii) a light chain comprising CDRs 1, 2 and 3 (LCDR1, LCDR2, LCDR3), according to the Kabat definition, of the light chain variable region sequence of SEQ ID NO: 14. 2. The antibody of claim 1 , wherein said antibody comprises a human IgG heavy chain constant region. 3. The antibody of claim 1 , wherein said antibody is a chimeric, human or humanized antibody. 4. The antibody of claim 1 , wherein said antibody comprises a modified human heavy chain constant region with at least one amino acid substitution, wherein the binding affinity of said modified constant region to an FcγIIIA receptor is increased, compared to a constant region not having said amino acid substitution. 5. The antibody of claim 1 , wherein the antibody causes an increase of the amount of KIR3DL2 polypeptides detectable at the cell surface of a KIR3DL2-expressing cell. 6. The antibody of claim 1 , wherein said KIR3DL2-expressing cell is a CD4+ T cell lymphoma. 7. An antibody that competes for binding to a KIR3DL2 polypeptide with an antibody having respectively a VH and VL region of SEQ ID NOS: 13 and 14 (2B12), wherein the antibody that competes for binding to said KIR3DL2 polypeptide has (i) a heavy chain comprising CDRs 1, 2 and 3 (HCDR1, HCDR2, HCDR3), according to the Kabat definition, of the heavy chain variable region sequence of SEQ ID NO: 13, and (ii) a light chain comprising CDRs 1, 2 and 3 (LCDR1, LCDR2, LCDR3), according to the Kabat definition, of the light chain variable region sequence of SEQ ID NO: 14. 8. The antibody of claim 7 , wherein the antibody causes an increase of the amount of KIR3DL2 polypeptides detectable at the cell surface of a KIR3DL2-expressing cell. 9. The antibody of claim 7 , wherein said KIR3DL2-expressing cell is a CD4+ T cell lymphoma. 10. A pharmaceutical composition comprising the antibody of claim 1 and a pharmaceutically acceptable carrier.
Inflammation · CPC title
Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis · CPC title
Immunology or allergic disorders · CPC title
Immunoglobulin superfamily, e.g. VCAMs, PECAM, LFA-3 · CPC title
White blood cells · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.