自身免疫中的T细胞受体测序。

Angela M Mitchell, Aaron W Michels
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引用次数: 14

摘要

通过细胞表面表达的T细胞受体(TCR)对肽的识别,T细胞是适应性免疫反应的一个组成部分。TCR基因的重排导致在给定个体的T细胞上高度多态性的曲目。尽管多样化的储备有利于免疫应答外来病原体,但T细胞对自身肽的识别可能有助于自身免疫性疾病的发展。越来越多的证据支持T细胞在自身免疫性病理中的致病作用,确定参与自身免疫性疾病发展的TCR谱是有意义的。在这篇综述中,我们总结了TCR测序领域的方法和进展,并讨论了最近在各种自身免疫性疾病中TCR测序的研究。快速发展的TCR测序方法有可能使我们更好地了解自身免疫性疾病的发病机制,识别疾病特异性生物标志物,并帮助开发预防和治疗许多这些疾病的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T cell receptor sequencing in autoimmunity.

T cells are an integral component of the adaptive immune response via the recognition of peptides by the cell surface-expressed T cell receptor (TCR). Rearrangement of the TCR genes results in a highly polymorphic repertoire on the T cells within a given individual. Although the diverse repertoire is beneficial for immune responses to foreign pathogens, recognition of self-peptides by T cells can contribute to the development of autoimmune disorders. Increasing evidence supports a pathogenic role for T cells in autoimmune pathology, and it is of interest to determine the TCR repertoires involved in autoimmune disease development. In this review, we summarize methodologies and advancements in the TCR sequencing field and discuss recent studies focused on TCR sequencing in a variety of autoimmune conditions. The rapidly evolving methodology of TCR sequencing has the potential to allow for a better understanding of autoimmune disease pathogenesis, identify disease-specific biomarkers, and aid in developing therapies to prevent and treat a number of these disorders.

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