Treatment of peripheral vascular disease using umbilical cord tissue-derived cells
US-2015374758-A1 · Dec 31, 2015 · US
US9598669B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9598669-B2 |
| Application number | US-64881206-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 28, 2006 |
| Priority date | Dec 29, 2005 |
| Publication date | Mar 21, 2017 |
| Grant date | Mar 21, 2017 |
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The present invention provides improved compositions and methods for the collection of stem cells from an organ, e.g., placenta. The invention provides a stem cell collection composition comprising an apoptosis inhibitor and, optionally, an enzyme such as a protease or mucolytic enzyme, vasodilator, necrosis inhibitor, oxygen-carrying perfluorocarbon, or an organ preserving compound. The invention provides methods of using the stem cell collection composition to collect stem cells and to preserve populations of stem cells.
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What is claimed is: 1. A composition comprising, in a physiologically-acceptable solution, a JNK inhibitor, wherein said JNK inhibitor is 3-(4-fluoro-phenyl)-1H-indazole-5-carboxylic acid amide; a protease; an oxygen-carrying perfluorocarbon; 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione; atrial natriuretic peptide (ANP); and either pyrrolidine dithiocarbamate or clonazepam; wherein said composition is not a naturally-occurring composition, and wherein said JNK inhibitor is an inhibitor of apoptosis; and wherein the composition is suitable for collecting placental stem cells. 2. The composition of claim 1 , wherein said protease is present in an amount sufficient to detectably dissociate cells of a tissue comprising stem cells. 3. The composition of claim 1 wherein said physiologically-acceptable solution is a saline solution or culture medium. 4. The composition of claim 3 wherein said saline solution is 0.9% NaCl solution or phosphate buffered saline. 5. The composition of claim 1 , wherein said protease is a matrix metalloprotease or a neutral protease. 6. The composition of claim 5 , wherein said matrix metalloprotease is collagenase. 7. The composition of claim 5 , wherein said neutral protease is thermolysin or dispase. 8. The composition of claim 1 , wherein said composition comprises hyaluronidase. 9. The composition of claim 1 , additionally comprising hydroxyethyl starch, lactobionic acid and raffinose. 10. The composition of claim 1 , additionally comprising UW solution. 11. The composition of claim 1 , wherein said JNK inhibitor is an indazole. 12. The composition of claim 1 comprising a plurality of stem cells. 13. The composition of claim 12 , wherein said stem cells comprise CD34 + stem cells. 14. The composition of claim 13 , wherein said CD34 + stem cells comprise CD34 + CD38 − stem cells. 15. The composition of claim 13 , wherein said CD34 + CD38 − stem cells are part of a population of CD34 + CD38 − stem cells present in placental perfusate as a higher percentage of total nucleated cells as compared to the percentage of CD34 + CD38 − cells in cord blood. 16. The composition of claim 12 , wherein said stem cells are CD34 − stem cells. 17. The composition of claim 16 , wherein said CD34 − stem cells are additionally HLA-G + or CD200 + . 18. The composition of claim 16 , wherein said CD34 − stem cells are additionally OCT-4 + , CD73 + , or CD105+.
Regulators of apoptosis · CPC title
Cells from extra-embryonic tissues, e.g. placenta, amnion, yolk sac, Wharton's jelly · CPC title
Small molecules not provided for elsewhere · CPC title
Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor; (plant reproduction by tissue culture techniques A01H4/00) · CPC title
Non-embryonic pluripotent stem cells, e.g. MASC (induced pluripotent stem cells C12N5/0696) · CPC title
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