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Publication : Cutting edge: regulatory T cells do not mediate suppression via programmed cell death pathways.

First Author  Szymczak-Workman AL Year  2011
Journal  J Immunol Volume  187
Issue  9 Pages  4416-20
PubMed ID  21949016 Mgi Jnum  J:179446
Mgi Id  MGI:5302440 Doi  10.4049/jimmunol.1100548
Citation  Szymczak-Workman AL, et al. (2011) Cutting edge: Regulatory T cells do not mediate suppression via programmed cell death pathways. J Immunol 187(9):4416-20
abstractText  Regulatory T cells (Tregs) play a critical role in the immune system to regulate peripheral tolerance and prevent autoimmunity. However, the relative importance of different mechanisms of Treg function remains obscure. In this article, we reveal a limited role for programmed cell death pathways in mediating Treg suppression of conventional T cells. We show that Tregs are able to suppress the proliferation of conventional T cells that are resistant to apoptosis (Bim(-/-), Bim(-/-)Puma(-/-), Bcl-2 transgenic) or receptor-interacting serine-threonine kinase-dependent necrosis (also referred to as regulated necrosis or necroptosis) (Ripk3(-/-)) in several in vitro and in vivo assays. These data suggest that programmed cell death pathways, such as apoptosis and receptor-interacting serine-threonine kinase-dependent necrosis, are not required for Treg-mediated suppression.
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