Mesenchymal stem cells for the treatment of cns diseases
US-2018333458-A1 · Nov 22, 2018 · US
US10869899B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10869899-B2 |
| Application number | US-201715820521-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 22, 2017 |
| Priority date | Jun 16, 2005 |
| Publication date | Dec 22, 2020 |
| Grant date | Dec 22, 2020 |
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An isolated human cell and populations thereof is provided comprising at least one astrocytic phenotype and at least one mesenchymal stem cell phenotype, wherein the mesenchymal stem cell phenotype is not an astrocytic phenotype.
Opening claim text (preview).
What is claimed is: 1. An isolated cell population comprising human cells which express CD90, and secrete glial derived neurotrophic factor (GDNF), wherein a secretion of said GDNF is at least 2 times greater than a basal secretion of said GDNF in non-differentiated mesenchymal stem cells, wherein the cell population is non-genetically modified, and wherein the cell population has been differentiated ex vivo from human mesenchymal stem cells. 2. The isolated cell population of claim 1 , wherein said human cells co-express said CD90 and glial fibrillary acidic protein (GFAP). 3. The isolated cell population of claim 1 , wherein a secretion of said GDNF is at least 5 times greater than a basal secretion of said neurotrophic factor in said non-differentiated mesenchymal stem cells. 4. The isolated cell population of claim 1 , wherein said human cells have a star-shaped body. 5. The isolated cell population of claim 1 , further secreting at least one neurotrophic factor selected from the group consisting of brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), neurotrophin-4/5, Neurturin (NTN), Persephin, artemin (ART), ciliary neurotrophic factor (CNTF), insulin growth factor-I (IGF-1) and Neublastin. 6. The isolated cell population of claim 1 , wherein a secretion of said GDNF is upregulated by IL-1 beta and/or cabergoline. 7. A pharmaceutical composition comprising the isolated cell population of claim 1 . 8. A device comprising the pharmaceutical composition of claim 7 , the device being adapted for administration of the isolated cell population into the spinal cord. 9. A device comprising the pharmaceutical composition of claim 7 , the device being adapted for administration of the isolated cell population into the brain. 10. A device comprising the pharmaceutical composition of claim 7 , the device being adapted for intramuscular administration of the isolated cell population.
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