Devi K Sanjana P, Anandasabapathy Niroshana
Department of Dermatology/Harvard Skin Disease Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Semin Immunopathol. 2017 Feb;39(2):137-152. doi: 10.1007/s00281-016-0602-0. Epub 2016 Nov 25.
Dendritic cells (DCs) are specialized immune sentinels that play key role in maintaining immune homeostasis by efficiently regulating the delicate balance between protective immunity and tolerance to self. Although DCs respond to maturation signals present in the surrounding milieu, multiple layers of suppression also co-exist that reduce the infringement of tolerance against self-antigens. These tolerance inducing properties of DCs are governed by their origin and a range of other factors including distribution, cytokines, growth factors, and transcriptional programing, that collectively impart suppressive functions to these cells. DCs directing tolerance secrete anti-inflammatory cytokines and induce naïve T cells or B cells to differentiate into regulatory T cells (Tregs) or B cells. In this review, we provide a detailed outlook on the molecular mechanisms that induce functional specialization to govern central or peripheral tolerance. The tolerance-inducing nature of DCs can be exploited to overcome autoimmunity and rejection in graft transplantation.
树突状细胞(DCs)是特殊的免疫哨兵,通过有效调节保护性免疫和自身耐受性之间的微妙平衡,在维持免疫稳态中发挥关键作用。尽管DCs对周围环境中存在的成熟信号作出反应,但也存在多层抑制机制,以减少对自身抗原耐受性的侵犯。DCs的这些诱导耐受性的特性受其起源以及一系列其他因素的支配,这些因素包括分布、细胞因子、生长因子和转录编程,它们共同赋予这些细胞抑制功能。引导耐受性的DCs分泌抗炎细胞因子,并诱导初始T细胞或B细胞分化为调节性T细胞(Tregs)或B细胞。在这篇综述中,我们详细阐述了诱导功能特化以控制中枢或外周耐受性的分子机制。DCs的诱导耐受性特性可被利用来克服自身免疫和移植排斥反应。