Briseño Carlos G, Murphy Theresa L, Murphy Kenneth M
Department of Pathology and Immunology, Washington University in St. Louis, School of Medicine, 660 S. Euclid Avenue, St. Louis, MO 63110, USA.
Department of Pathology and Immunology, Washington University in St. Louis, School of Medicine, 660 S. Euclid Avenue, St. Louis, MO 63110, USA; Howard Hughes Medical Institute, Washington University in St. Louis, School of Medicine, 660 S. Euclid Avenue, St. Louis, MO 63110, USA.
Curr Opin Immunol. 2014 Aug;29:69-78. doi: 10.1016/j.coi.2014.04.006. Epub 2014 May 27.
Dendritic cells (DCs) are professional antigen presenting cells conventionally thought to mediate cellular adaptive immune responses. Recent studies have led to the recognition of a non-redundant role for DCs in orchestrating innate immune responses, and in particular, for DC subset-specific interactions with innate lymphoid cells (ILCs). Recently recognized as important effectors of early immune responses, ILCs develop into subsets which mirror the transcriptional and cytokine profile of their T cell subset counterparts. DC diversification into functional subsets provides for modules of pathogen sensing and cytokine production that direct pathogen-appropriate ILC and T cell responses. This review focuses on the recent advances in the understanding of DC development, and their function in orchestrating the innate immune modules.
树突状细胞(DCs)是传统上被认为介导细胞适应性免疫反应的专职抗原呈递细胞。最近的研究已使人们认识到DCs在协调先天性免疫反应中具有不可替代的作用,尤其是在DC亚群与先天性淋巴细胞(ILCs)的特异性相互作用方面。ILCs最近被认为是早期免疫反应的重要效应器,它们分化为多个亚群,这些亚群反映了其对应的T细胞亚群的转录和细胞因子谱。DCs分化为功能亚群,形成了病原体感知和细胞因子产生模块,这些模块指导针对病原体的适当ILC和T细胞反应。本综述重点关注DC发育理解方面的最新进展及其在协调先天性免疫模块中的功能。