US2017157181A1PendingUtilityA1
Methods of generating, repairing and/or maintaining connective tissue in vivo
Est. expiryAug 6, 2027(~1.1 yrs left)· nominal 20-yr term from priority
Inventors:Peter Ghosh
A61P 43/00A61P 25/00A61P 25/02A61P 29/00A61P 25/04A61K 47/36A61K 2300/00A61K 35/28A61P 19/02A61K 31/726A61P 19/04A61P 1/04A61K 31/728A61K 2035/124A61K 35/545A61K 38/14C12N 5/0663A61P 19/00A61P 21/00A61K 9/4866C12N 2501/905A61K 31/737A61P 17/06A61K 35/12A61P 19/08A61L 2430/38A61L 27/52A61L 27/3856A61L 27/3834A61K 31/727
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Claims
Abstract
This invention relates to a method for generating, repairing and/or maintaining connective tissue in a subject. In one embodiment, the invention relates to a method for generating, repairing and/or maintaining cartilage tissue in a subject. The present invention also relates to a method of treating and/or preventing a disease in a subject arising from degradation and inflammation of connective tissue.
Claims
exact text as granted — not AI-modified1 - 15 . (canceled)
16 . A therapeutic composition comprising a population of human cells enriched for STRO-1 bright mesenchymal precursor cells (MPCs) or culture-expanded multipotent progeny thereof; and chondroprotective agent.
17 . The therapeutic composition of claim 16 , wherein the chondroprotective agent comprises an chondroprotective agent selected from the group consisting of: pentosan polysulfate, glycosaminoglycan polysufate ester, glyciamino-glycan-peptide complex, and Hyaluronic Acid (HA).
18 . The therapeutic composition of claim 17 , wherein the chondroprotective agent comprises HA.
19 . The therapeutic composition of claim 16 , further comprising a cryoprotectant.
20 . The therapeutic composition of claim 16 , wherein the MPCs carry at least one additional marker selected from the group of surface markers consisting of THY-1, VCAM-1, STRO-2, TNAP, and CD146.
21 . The therapeutic composition of claim 20 , wherein the MPCs carry the marker TNAP.
22 . The therapeutic composition of claim 16 , further comprising an in situ-polymerizable gel.
23 . The therapeutic composition of claim 22 , wherein the in situ-polymerizable gel comprises alginate.
24 . The therapeutic composition of claim 16 , wherein the population is encapsulated.
25 . The therapeutic composition of claim 16 , wherein the population is an allogeneic population.
26 . The therapeutic composition of claim 16 , wherein the population is an autologous population.
27 . The therapeutic composition of claim 16 , wherein the population is a genetically modified population.
28 . The therapeutic composition of claim 27 , wherein the cells in the genetically modified population comprise an exogenous polynucleotide that encodes a selective marker, a cytokine, or a chemokine.
29 . The therapeutic composition of claim 16 , wherein the STRO-1 bright cells are STRO-1 bright cells enriched from bone marrow.Cited by (0)
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