Asgpr-binding compounds for the degradation of extracellular proteins
US-2024424108-A1 · Dec 26, 2024 · US
US9732134B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9732134-B2 |
| Application number | US-201213672417-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 8, 2012 |
| Priority date | Jan 21, 2009 |
| Publication date | Aug 15, 2017 |
| Grant date | Aug 15, 2017 |
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Described herein are immunosuppressive molecules including immunosuppressive variants of IL-2, and use of such molecules to treat inflammatory and autoimmune disorders.
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What is claimed is: 1. A method of treating graft versus host disease in a subject, said method comprising administering to a subject in need thereof a therapeutically effective amount of an IL-2 variant comprising a sequence of amino acids that differs from SEQ ID NO: 1 only at one or more of residues E15, H16, Q22, D84, N88, or E95, wherein said IL-2 variant selectively promotes FOXP3-positive regulatory T cell growth or survival in vitro. 2. The method of claim 1 , wherein the IL-2 variant induces STAT5 phosphorylation in ex vivo FOXP3-positive T cells comprising a functional IL-2 receptor complex but has a reduced ability to induce phosphorylation of STAT5 in FOXP3-negative T cells. 3. The method of claim 1 , wherein the IL-2 variant is conjugated to a chemical or polypeptide that extends the serum half-life of said IL-2 variant in vivo.
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