| Literature DB >> 26111522 |
Fang Zhou1,2, Guang-Xian Zhang3, Abdolmohamad Rostami4.
Abstract
CD4(+) memory T cells play an important role in induction of autoimmunity and chronic inflammatory responses; however, regulatory mechanisms of CD4(+) memory T cell-mediated inflammatory responses are poorly understood. Here we show that apoptotic cell-treated dendritic cells inhibit development and differentiation of CD4(+) effector memory T cells in vitro and in vivo. Simultaneously, intravenous transfer of apoptotic T cell-induced tolerogenic dendritic cells can block development of experimental autoimmune encephalomyelitis (EAE), an inflammatory disease of the central nervous system in C57 BL/6J mouse. Our results imply that it is effector memory CD4(+) T cells, not central memory CD4(+) T cells, which play a major role in chronic inflammatory responses in mice with EAE. Intravenous transfer of tolerogenic dendritic cells induced by apoptotic T cells leads to immune tolerance by specifically blocking development of CD4(+) effector memory T cells compared with results of EAE control mice. These results reveal a new mechanism of apoptotic cell-treated dendritic cell-mediated immune tolerance in vivo.Entities:
Keywords: Apoptosis; Autoimmunity; Dendritic cell; Immune tolerance; Immunotherapy; Inflammation; Memory T cell
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Year: 2016 PMID: 26111522 PMCID: PMC4691443 DOI: 10.1007/s12026-015-8676-7
Source DB: PubMed Journal: Immunol Res ISSN: 0257-277X Impact factor: 2.829