Compositions and methods comprising histidyl-tRNA synthetase splice variants having non-canonical biological activities
US-10526419-B2 · Jan 7, 2020 · US
US11078299B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11078299-B2 |
| Application number | US-202016842195-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 7, 2020 |
| Priority date | Mar 16, 2009 |
| Publication date | Aug 3, 2021 |
| Grant date | Aug 3, 2021 |
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Isolated histidyl-tRNA synthetase splice variant polynucleotides and polypeptides having non-canonical biological activities are provided, as well as compositions and methods related thereto.
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The invention claimed is: 1. A method of treating a viral respiratory infection in a subject in need thereof, comprising administering to the subject a pharmaceutical composition, comprising a physiologically acceptable carrier and a fusion polypeptide, wherein the fusion polypeptide comprises a histidyl-tRNA synthetase (HRS) polypeptide fused to an Fc fragment, wherein the FIRS polypeptide consists of a sequence that has at least 95% identity along its length to SEQ ID NO: 6, comprises a WHEP domain, and lacks a functional aminoacylation domain. 2. The method of claim 1 , wherein the FIRS polypeptide consists of a sequence that has at least 98% identity along its length to SEQ ID NO: 6. 3. The method of claim 1 , wherein the N-terminal region of the HRS polypeptide polypeptide is truncated by 1, 2, or 3 amino acids. 4. The method of claim 1 , wherein the fusion polypeptide reduces cell migration of monocytes/macrophages in the subject in need thereof. 5. The method of claim 1 , comprising intravenously administering the pharmaceutical composition to the subject. 6. The method of any one of claims 1 - 5 , wherein the viral respiratory infection comprises a Severe Acute Respiratory Syndrome (SARS) infectious agent.
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