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We aimed to evaluate the immunosuppressive ramifications of human amnion-derived MSC (AMSC) in a xenogeneic GVHD NOD/Shi-scid IL2rγnull mouse model using human peripheral blood mononuclear cells (PBMC). Also, we utilized human being bone tissue marrow-derived MSC (BMSC) as relative settings to ascertain variations in immunomodulatory features according to the MSC source. Management of AMSC significantly prolonged survival, and paid down human being tumor

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