Apoptotic cell-treated dendritic cells induce immune tolerance by specifically inhibiting development of CD4+ effector memory T cells

被引:0
|
作者
Fang Zhou
Guang-Xian Zhang
Abdolmohamad Rostami
机构
[1] Thomas Jefferson University,Department of Neurology
[2] University of Queensland,Laboratory of Liver Cancer Immunotherapy, Greenslopes Private Hospital, School of Medicine
来源
Immunologic Research | 2016年 / 64卷
关键词
Dendritic cell; Immune tolerance; Immunotherapy; Memory T cell; Autoimmunity; Inflammation; Apoptosis;
D O I
暂无
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学科分类号
摘要
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.
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页码:73 / 81
页数:8
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