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- W2051277340 abstract "Abstract Previous work has demonstrated that both rapamycin (RAPA) and IL-2 enhance CD4+CD25+Foxp3+ regulatory T-cell (Treg) proliferation and function in vitro. We investigated whether the combination of RAPA plus IL-2 could impact acute GVHD induction after bone marrow transplantation (BMT). RAPA plus IL-2 resulted in improved survival and a reduction in acute GVHD lethality associated with an increased expansion of donor type CD4+Foxp3+ Tregs and reduced CD4+CD25− conventional T cells (Tcons). RAPA plus IL-2, but not either drug alone, increased both expansion of donor natural Tregs and conversion of induced Tregs from donor CD25− Tcons while IL-2 alone increased conversion of Tregs from CD25− Tcon. RAPA plus IL-2 treatment resulted in less production of IFN-γ and TNF, cytokines known to be important in the initiation of acute GVHD. These studies indicate that the pharmacologic stimulation of T cells with IL-2 and the suppression of Tcon proliferation with RAPA result in a selective expansion of functional Tregs and suppression of acute GVHD." @default.
- W2051277340 created "2016-06-24" @default.
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- W2051277340 date "2011-08-25" @default.
- W2051277340 modified "2023-10-06" @default.
- W2051277340 title "Rapamycin and IL-2 reduce lethal acute graft-versus-host disease associated with increased expansion of donor type CD4+CD25+Foxp3+ regulatory T cells" @default.
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- W2051277340 doi "https://doi.org/10.1182/blood-2010-10-313684" @default.
- W2051277340 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4467868" @default.
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