Compositions and methods comprising histidyl-tRNA synthetase splice variants having non-canonical biological activities
US-9605265-B2 · Mar 28, 2017 · US
US10017582B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10017582-B2 |
| Application number | US-201615257353-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 6, 2016 |
| Priority date | Mar 16, 2009 |
| Publication date | Jul 10, 2018 |
| Grant date | Jul 10, 2018 |
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.
Isolated histidyl-tRNA synthetase splice variant polynucleotides and polypeptides having non-canonical biological activities are provided, as well as compositions and methods related thereto.
Opening claim text (preview).
The invention claimed is: 1. A method of reducing a cancer or malignancy, comprising administering to a subject in need thereof a composition comprising a pharmaceutically-acceptable carrier and an antibody or antigen-binding fragment thereof that exhibits binding specificity for a histidyl-tRNA synthetase (HRS) splice variant polypeptide consisting of a sequence set forth in SEQ ID NO:6, 9, or 11, or a fragment of SEQ ID NO:6, 9, or 11, wherein the antibody or antigen-binding fragment thereof is at least about 90% pure. 2. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof antagonizes a non-canonical activity of the HRS splice variant polypeptide. 3. The method of claim 1 , wherein the fragment of SEQ ID NO:6, 9, or 11 consists of the WHEP domain of HRS. 4. The method of claim 1 , wherein the fragment of SEQ ID NO:9 or 11 consists of the anticodon binding domain of HRS. 5. The method of claim 1 , wherein the antibody or antigen binding fragment thereof is a monoclonal antibody. 6. The method of claim 1 , wherein the antibody is a humanized antibody. 7. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof is an Fv fragment or a single chain Fv (sFv) polypeptide. 8. The method of claim 1 , wherein the composition is a sterile injectable solution. 9. The method of claim 1 , wherein the composition is buffered and comprises an isotonic agent. 10. The method of claim 1 , wherein the composition is suitable for intravenous, intramuscular, subcutaneous, or intraperitoneal administration. 11. The method of claim 1 , wherein the composition comprises a surfactant. 12. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof is at least about 95% pure.
Immunomodulators · CPC title
Immunosuppressants, e.g. drugs for graft rejection · CPC title
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Drugs for disorders of the cardiovascular system · CPC title
Drugs for disorders of the nervous system · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.