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Rapamycin selectively expands CD4(+)CD25(+)FoxP3(+) regulatory T cells

Academic Article
Publication Date:
2005
abstract:
Rapamycin is an immunosuppressive compound that is currently used to prevent acute graft rejection in humans. In addition, rapamycin has been shown to allow operational tolerance in murine models. However, a direct effect of rapamycin on T regulatory (Tr) cells, which play a key role in induction and maintenance of peripheral tolerance, has not been demonstrated so far. Here, we provide new evidence that rapamycin selectively expands the murine naturally occurring CD4(+)CD25(+)FoxP3(+) Tr cells in vitro. These expanded Tr cells suppress proliferation of syngeneic T cells in vitro and prevent allograft rejection in vivo. Interestingly, rapamycin does not block activation-induced cell death and proliferation of CD4(+) T cells in vitro. Based on this new mode of action, rapamycin can be used to expand CD4(+)CD25(+)FoxP3(+) Tr cells for ex vivo cellular therapy in T-cell-mediated diseases. (c) 2005 by The American Society of Hematology.
Iris type:
1.1 Articolo in rivista
List of contributors:
Battaglia, Marco Maria; Stabilini, A; Roncarolo, Maria Grazia
Handle:
https://iris.unisr.it/handle/20.500.11768/2882
Published in:
BLOOD
Journal
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