US2014170116A9PendingUtilityA9
Method of treating ischemic disorders
Est. expiryAug 22, 2022(expired)· nominal 20-yr term from priority
Inventors:Marc S. Penn
A61P 7/02A61P 43/00A61P 9/10A61K 48/0075A61K 35/28A61P 11/00A61K 38/195A61P 13/12
56
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Claims
Abstract
A method of treating an ischemic disorders in a subject includes administering stromal cell derived factor-1 (SDF-1) to ischemic tissue of the subject in an amount effective to inhibit apoptosis of cells of the tissue.
Claims
exact text as granted — not AI-modified1 . A method of treating an ischemic disorders in a subject, the method comprising administering stromal cell derived factor-1 (SDF-1) to ischemic tissue of the subject in an amount effective to inhibit apoptosis of cells of the tissue.
2 . The method of claim 1 , the SDF-1 being administered to cells including SDF-1 receptors that are up-regulated as a result of the ischemic disorder.
3 . The method of claim 2 , the SDF-1 receptor comprising CXCR4.
4 . The method of claim 1 , the SDF-1 being administered at amount effect to increase Akt-phosphorylation of the cells.
5 . The method of claim 1 , the SDF-1 being administered by expressing SDF-1 in the tissue being treated.
6 . The method of claim 5 , the SDF-1 being expressed from a cell that is biocomaptible with the ischemic tissue being treated.
7 . The method of claim 5 , the SDF-1 being expressed from a cell of the ischemic tissue or a cell about the periphery of the ischemic tissue.
8 . The method of claim 7 , the cell expressing the SDF-1 being genetically modified by at least one of a vector, plasmid DNA, electroporation, and nano-particles to express SDF-1.
9 . The method of claim 1 , further comprising administering MCP-3 to the ischemic tissue at amount effective to recruit stem cells an/or progenitor cells to the ischemic tissue.
10 . The method of claim 9 , the stem cells comprising autologous and/or syngeneic mesenchymal stem cells.
11 - 16 . (canceled)
17 . The method of claim 1 , the ischemic disorder comprising at least one of a peripheral vascular disorder, a pulmonary embolus, a venous thrombosis, a myocardial infarction, a transient ischemic attack, unstable angina, cerebral vascular ischemia, a reversible ischemic neurological deficit, ischemic kidney disease, or a stroke disorder.
18 . A method of mitigating apoptosis in cells of a tissue following tissue injury, comprising administering to cells of the tissue an amount of SDF-1 effective to inhibit apoptosis in the cells.
19 . The method of claim 18 , the cells including SDF-1 receptors that are up-regulated as a result of the ischemic disorder.
20 . The method of claim 19 , the SDF-1 receptor comprising CXCR4.
21 . The method of claim 18 , the SDF-1 being administered at amount effect to increase Akt-phosphorylation of the cells.
22 . The method of claim 18 , the SDF-1 being administered by expressing SDF-1 in the tissue.
23 . The method of claim 22 , the SDF-1 being expressed from a cell that is biocomaptible with the tissue.
24 . The method of claim 18 , the SDF-1 being expressed from a cell of the tissue or a cell about the periphery of the tissue.
25 . The method of claim 23 , the cell expressing the SDF-1 being genetically modified by at least one of a vector, plasmid DNA, electroporation, and nano-particles to express SDF-1.
26 - 49 . (canceled)
50 . A method of mitigating apoptosis of cells or tissue transplanted to a subject being treating, comprising
administering SDF-1 to cells or tissue to be transplanted to the subject being treated, the cells or tissue expressing an SDF-1 receptor.
51 . The method of claim 50 , the SDF-1 being administered to the cells or tissue prior to transplantation of the subject being treated.
52 . The method of claim 50 , the SDF-1 being administered to the cells or tissue during and/or after transplantation of the cells.
53 . The method of claim 50 , the SDF-1 receptor comprising CXCR4.
54 . The method of claim 50 , the SDF-1 being administered at amount effect to increase Akt-phosphorylation of the apoptotic cells.
55 . The method of claim 50 , the cells comprising stem cells and/or progenitor cells expressing SDF-1 receptor.Cited by (0)
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