CPC C12N 5/0619 (2013.01) [A61K 9/5176 (2013.01); A61K 35/12 (2013.01); A61K 35/545 (2013.01); C12N 5/0622 (2013.01); C12N 5/0623 (2013.01); A61K 9/5068 (2013.01); A61K 35/30 (2013.01); A61P 25/28 (2018.01); C12N 2506/02 (2013.01); C12N 2506/45 (2013.01); C12N 2533/30 (2013.01); G01N 33/56966 (2013.01)] | 26 Claims |
1. A method of reducing inflammation in the brain of a subject, comprising administering to the subject an effective amount of a pharmaceutical composition comprising isolated extracellular vesicles (EVs) derived from non-transformed human neural progenitor cells that are capable of differentiating into neurons, astrocytes and oligodendrocytes in vitro, wherein the EVs are produced from neural progenitor cells derived in vitro from pluripotent stem cells, or from neural cells derived in vitro from the neural progenitor cells or the pluripotent stem cells,
and wherein the EVs comprise one or more of melanoma-associated chondroitin sulfate proteoglycan (MCSP), pentraxin-3 (PTX3), angiopoietin-1, insulin-like growth factor-binding protein 2 (IGFBP2), macrophage colony-stimulating factor, and ecto-5′-nucleotidase (NT5E).
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