4.4 Article

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

Journal

IMMUNOLOGIC RESEARCH
Volume 64, Issue 1, Pages 73-81

Publisher

HUMANA PRESS INC
DOI: 10.1007/s12026-015-8676-7

Keywords

Dendritic cell; Immune tolerance; Immunotherapy; Memory T cell; Autoimmunity; Inflammation; Apoptosis

Categories

Funding

  1. NCI NIH HHS [P30 CA056036] Funding Source: Medline
  2. NIAID NIH HHS [R01 AI106026] Funding Source: Medline
  3. NINDS NIH HHS [R01 NS075260, R01 NS048435] Funding Source: Medline

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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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