Genetically modified porcine cells, tissue, and animals with reduced human xenoreactivity and methods of using the same
US-2024271103-A1 · Aug 15, 2024 · US
US10016463B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10016463-B2 |
| Application number | US-201314418557-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 30, 2013 |
| Priority date | Aug 1, 2012 |
| Publication date | Jul 10, 2018 |
| Grant date | Jul 10, 2018 |
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The current application is directed to a method for treating pulmonary arterial hypertension (PAH), comprising: providing isolated endothelial progenitor cells (EPCs); treating the EPCs with prostacyclin, wherein the treated EPCs exhibit a hyperproliferative phenotype with enhanced angiogenic property; and administering a composition comprising the treated EPCs into a subject suffering from PAH.
Opening claim text (preview).
What is claimed is: 1. A method for treating pulmonary hypertension, comprising: providing isolated endothelial progenitor cells (EPCs), wherein the EPCs are isolated from a human being, a tissue, or cell culture; treating the isolated EPCs in vitro or ex vivo with a prostacyclin during expansion of the EPCs, wherein the treated EPCs exhibit a hyperproliferative phenotype with enhanced angiogenic activity; and administering a composition comprising the treated EPCs to a subject suffering from pulmonary hypertension. 2. The method of claim 1 , wherein the prostacyclin is selected from the group consisting of epoprostenol sodium, treprostinil, and iloprost. 3. The method of claim 1 , wherein the subject is a human being. 4. The method of claim 1 , wherein the EPCs are autologous. 5. The method of claim 1 , wherein the EPCs are isolated from the blood of the subject suffering from pulmonary hypertension. 6. The method of claim 1 , wherein the EPCs are endothelial colony forming cells. 7. The method of claim 1 , wherein the EPCs are genetically modified. 8. The method of claim 1 , wherein the composition is a pharmaceutical composition further comprising at least one pharmaceutically-acceptable carrier. 9. The method of claim 1 , wherein the composition further comprises at least one therapeutic agent other than EPCs. 10. The method of claim 1 , wherein administering the composition promotes pulmonary vascular repair. 11. The method of claim 1 , wherein the composition is co-administered with at least one growth factor. 12. The method of claim 11 , wherein the growth factor is selected from the group consisting of FGF, VEGF-A, VEGF-B, BMP-4, and TGF-Beta. 13. The method of claim 1 , wherein the composition is co-administered with (i) mesenchymal stem cells or (ii) a culture medium that has been in contact with mesenchymal stem cells and that contains one or more components thereof. 14. The method of claim 1 , wherein the composition is co-administered with a prostacyclin. 15. The method of claim 5 , wherein the subjected is pretreated with a prostacyclin before the isolation of the EPCs. 16. The method of claim 1 , wherein the prostacyclin is treprostinil.
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