Methods and materials for identifying and treating membranous nephropathy
US-2024353404-A1 · Oct 24, 2024 · US
US2017190791A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017190791-A1 |
| Application number | US-201615363084-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 29, 2016 |
| Priority date | Apr 26, 2010 |
| Publication date | Jul 6, 2017 |
| Grant date | — |
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Provided are compositions comprising newly identified protein fragments of aminoacyl-tRNA synthetases, polynucleotides that encode them and complements thereof, related agents, and methods of use thereof in diagnostic, drug discovery, research, and therapeutic applications.
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1 - 125 . (canceled) 126 . A therapeutic composition, comprising a pharmaceutically-acceptable carrier and an antibody or antigen-binding fragment thereof that exhibits binding specificity for an isolated aminoacyl-tRNA synthetase (AARS) polypeptide or an epitope selected from Table(s) 1-3, or Table(s) 4-6, and Table(s) 7-9, wherein the composition has a purity of at least about 90% on a protein basis and less than about 10 EU endotoxin/mg protein. 127 . The therapeutic composition of claim 126 , wherein the AARS polypeptide is selected from Table E7. 128 . The therapeutic composition of claim 126 , wherein the antibody or antigen binding fragment thereof is a monoclonal antibody. 129 . The therapeutic composition of claim 126 , wherein the antibody is a humanized antibody. 130 . The therapeutic composition of claim 126 , wherein the antibody or antigen-binding fragment thereof is an Fv fragment or a single chain Fv (sFv) polypeptide. 131 . The therapeutic composition of claim 126 , wherein the composition is a sterile, freeze-dried powder. 132 . The therapeutic composition of claim 126 , wherein the composition is a sterile injectable solution. 133 . The therapeutic composition of claim 126 , wherein the composition is buffered and comprises an isotonic agent. 134 . The therapeutic composition of claim 126 , wherein the composition is suitable for intravenous, intramuscular, subcutaneous, or intraperitoneal administration. 135 . The therapeutic composition of claim 126 , wherein the composition comprises a surfactant. 136 . The therapeutic composition of claim 126 , wherein the composition has a purity of at least about 95% on a protein basis. 137 . A method of modulating a cellular activity of a cell, or protein, comprising contacting the cell or protein with a therapeutic composition of claim 126 . 138 . The method of claim 137 , wherein the cellular activity is selected from cell proliferation, cell differentiation, cell signaling, gene transcription, angiogenesis, cell binding, metabolism, cytokine production or activity, cytokine receptor activity, and inflammation. 139 . The method of claim 137 , wherein the cell type is selected from the group consisting of pre-adipocytes, bone marrow, neutrophils, blood cells, hepatocytes, astrocytes, mesenchymal stem cells, and skeletal muscle cells. 140 . The method of claim 137 , wherein the cell is in a subject. 141 . The method of claim 140 , comprising treating the subject, wherein the subject has a condition associated with a neoplastic disease, an immune system disease or condition, an inflammatory disorder, an infectious disease, a metabolic disease, neuronal/neurological disease, a muscular/cardiovascular disease, a disease associated with aberrant hematopoiesis, a disease associated with aberrant angiogenesis, or a disease associated with aberrant cell survival.
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