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Mechanisms of Innate Lymphoid Cell and Natural Killer T Cell Activation during Mucosal Inflammation

机译:粘膜炎症期间先天淋巴细胞和自然杀伤T细胞活化的机制

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摘要

Mucosal surfaces in the airways and the gastrointestinal tract are critical for the interactions of the host with its environment. Due to their abundance at mucosal tissue sites and their powerful immunomodulatory capacities, the role of innate lymphoid cells (ILCs) and natural killer T (NKT) cells in the maintenance of mucosal tolerance has recently moved into the focus of attention. While NKT cells as well as ILCs utilize distinct transcription factors for their development and lineage diversification, both cell populations can be further divided into three polarized subpopulations reflecting the distinction into Th1, Th2, and Th17 cells in the adaptive immune system. While bystander activation through cytokines mediates the induction of ILC and NKT cell responses, NKT cells become activated also through the engagement of their canonical T cell receptors (TCRs) by (glyco)lipid antigens (cognate recognition) presented by the atypical MHC I like molecule CD1d on antigen presenting cells (APCs). As both innate lymphocyte populations influence inflammatory responses due to the explosive release of copious amounts of different cytokines, they might represent interesting targets for clinical intervention. Thus, we will provide an outlook on pathways that might be interesting to evaluate in this context.
机译:气道和胃肠道中的粘膜表面对于主体与其环境的相互作用至关重要。由于它们在粘膜组织部位和其强大的免疫调节能力,先天淋巴细胞(ILC)和自然杀伤T(NKT)细胞在维持粘膜耐受性中的作用最近陷入了关注的焦点。虽然NKT细胞以及ILCs利用不同的转录因子的发展和谱系多样化,但是这种细胞群可以进一步分为三种偏振群,反射在适应性免疫系统中的区别区区分为TH1,TH2和TH17细胞。虽然通过细胞因子的旁观者激活介导ILC和NKT细胞反应的诱导,但是也通过由非典型MHC I喜欢分子呈现的(Glyco)脂质抗原(同源识别)来激活NKT细胞的激活抗原呈递细胞(APC)的CD1D。由于天生淋巴细胞群体影响由于大量不同细胞因子的爆炸性释放,它们可能代表临床干预的有趣目标。因此,我们将在这种情况下评估可能有趣的途径。

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