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先天淋巴细胞:十年进展。

Innate Lymphoid Cells: 10 Years On.

机构信息

Innate Pharma Research Labs, Innate Pharma, Marseille, France; Aix Marseille University, CNRS, INSERM, APHM, CIML, Hôpital de la Timone, Immunologie, Marseille-Immunopole, Marseille, France.

Jill Roberts Institute for Research in Inflammatory Bowel Disease, Joan and Sanford I. Weill Department of Medicine and Department of Microbiology and Immunology, Weill Cornell Medicine, Cornell University, New York, NY, USA.

出版信息

Cell. 2018 Aug 23;174(5):1054-1066. doi: 10.1016/j.cell.2018.07.017.

Abstract

Innate lymphoid cells (ILCs) are lymphocytes that do not express the type of diversified antigen receptors expressed on T cells and B cells. ILCs are largely tissue-resident cells and are deeply integrated into the fabric of tissues. The discovery and investigation of ILCs over the past decade has changed our perception of immune regulation and how the immune system contributes to the maintenance of tissue homeostasis. We now know that cytokine-producing ILCs contribute to multiple immune pathways by, for example, sustaining appropriate immune responses to commensals and pathogens at mucosal barriers, potentiating adaptive immunity, and regulating tissue inflammation. Critically, the biology of ILCs also extends beyond classical immunology to metabolic homeostasis, tissue remodeling, and dialog with the nervous system. The last 10 years have also contributed to our greater understanding of the transcriptional networks that regulate lymphocyte commitment and delineation. This, in conjunction with the recent advances in our understanding of the influence of local tissue microenvironments on the plasticity and function of ILCs, has led to a re-evaluation of their existing categorization. In this review, we distill the advances in ILC biology over the past decade to refine the nomenclature of ILCs and highlight the importance of ILCs in tissue homeostasis, morphogenesis, metabolism, repair, and regeneration.

摘要

先天淋巴细胞 (ILC) 是不表达 T 细胞和 B 细胞上表达的多样化抗原受体的淋巴细胞。ILC 主要是组织驻留细胞,并深深整合到组织的结构中。在过去十年中对 ILC 的发现和研究改变了我们对免疫调节的认识以及免疫系统如何有助于维持组织内稳态。我们现在知道,细胞因子产生的 ILC 通过例如在黏膜屏障处维持对共生菌和病原体的适当免疫反应、增强适应性免疫以及调节组织炎症,有助于多种免疫途径。至关重要的是,ILC 的生物学也超越了经典免疫学,涉及代谢稳态、组织重塑以及与神经系统的对话。过去十年也有助于我们更好地理解调节淋巴细胞承诺和分化的转录网络。这一点,加上我们对局部组织微环境对 ILC 可塑性和功能的影响的最新理解,导致对其现有分类的重新评估。在这篇综述中,我们总结了过去十年中 ILC 生物学的进展,以完善 ILC 的命名法,并强调 ILC 在组织内稳态、形态发生、代谢、修复和再生中的重要性。

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