Literature DB >> 26111522

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

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

Mesh:

Substances:

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


  32 in total

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Review 7.  Memory T cell subsets, migration patterns, and tissue residence.

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Journal:  Front Immunol       Date:  2013-05-14       Impact factor: 7.561

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Review 4.  Paving the way towards an effective treatment for multiple sclerosis: advances in cell therapy.

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Journal:  Cell Mol Immunol       Date:  2021-05-06       Impact factor: 22.096

5.  Non-small Cell Lung Cancer Cells Modulate the Development of Human CD1c+ Conventional Dendritic Cell Subsets Mediated by CD103 and CD205.

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Review 6.  Molecular Mechanisms of Immunosenescene and Inflammaging: Relevance to the Immunopathogenesis and Treatment of Multiple Sclerosis.

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  7 in total

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