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经凋亡细胞处理的树突状细胞通过特异性抑制CD4⁺效应记忆T细胞的发育来诱导免疫耐受。

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

作者信息

Zhou Fang, Zhang Guang-Xian, Rostami Abdolmohamad

机构信息

Department of Neurology, Thomas Jefferson University, 901 Walnut Street, Philadelphia, PA, 19107, USA.

Laboratory of Liver Cancer Immunotherapy, Greenslopes Private Hospital, School of Medicine, University of Queensland, Greenslopes, Brisbane, QLD, 4120, Australia.

出版信息

Immunol Res. 2016 Feb;64(1):73-81. doi: 10.1007/s12026-015-8676-7.

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.

摘要

CD4(+)记忆T细胞在自身免疫和慢性炎症反应的诱导中起重要作用;然而,对CD4(+)记忆T细胞介导的炎症反应的调节机制了解甚少。在此我们表明,经凋亡细胞处理的树突状细胞在体外和体内均可抑制CD4(+)效应记忆T细胞的发育和分化。同时,静脉注射凋亡T细胞诱导的耐受性树突状细胞可阻断实验性自身免疫性脑脊髓炎(EAE)的发展,EAE是C57 BL/6J小鼠中枢神经系统的一种炎症性疾病。我们的结果表明,在患有EAE的小鼠的慢性炎症反应中起主要作用的是效应记忆CD4(+) T细胞,而非中枢记忆CD4(+) T细胞。与EAE对照小鼠的结果相比,静脉注射由凋亡T细胞诱导的耐受性树突状细胞可通过特异性阻断CD4(+)效应记忆T细胞的发育而导致免疫耐受。这些结果揭示了经凋亡细胞处理的树突状细胞在体内介导免疫耐受的新机制。

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