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肠道对外源抗原的免疫耐受:由CD4+T细胞介导的机制

Immune tolerance to foreign antigens in the intestine: mechanisms mediated by CD4+ T cells.

作者信息

Yoo Eunbi, Jo Yeleen, Park Jooyoun, Hong Sung-Wook

机构信息

Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Korea.

出版信息

BMB Rep. 2025 Apr;58(4):158-168. doi: 10.5483/BMBRep.2025-0009.

Abstract

The immune system encounters a diverse array of antigens, both self and foreign, necessitating mechanisms to maintain tolerance and prevent harmful inflammatory responses. CD4+ T cells, crucial in orchestrating immune responses, play a critical role in mediating tolerance to both self and foreign antigens. While the mechanisms of CD4+ T cell-mediated tolerance to self-antigens are well-documented, the understanding of tolerance to foreign antigens, including those from commensal microbes and food, remains incomplete. This review discusses recent progress in the mechanisms underlying immune tolerance to foreign antigens, with a focus on the role of CD4+ T cells. We explore how inflammatory and tolerogenic CD4+ T cell subsets are developed and maintained. Moreover, we delve into the complexities of immune responses to commensal microbes and food antigens by reviewing recent findings, highlighting the immunological contexts that shape immune tolerance. Understanding these mechanisms enhances our comprehension of how immune tolerance is established and sustained, providing insights into potential therapeutic approaches for managing chronic inflammatory diseases resulting from a loss of immune tolerance to foreign antigens. [BMB Reports 2025; 58(4): 158-168].

摘要

免疫系统会遇到各种各样的抗原,包括自身抗原和外来抗原,因此需要维持免疫耐受并防止有害炎症反应的机制。CD4+T细胞在协调免疫反应中至关重要,在介导对自身和外来抗原的耐受中发挥关键作用。虽然CD4+T细胞介导的对自身抗原耐受的机制已有充分记录,但对包括共生微生物和食物中的外来抗原的耐受的理解仍不完整。本综述讨论了对外来抗原免疫耐受机制的最新进展,重点是CD4+T细胞的作用。我们探讨了炎性和致耐受性CD4+T细胞亚群是如何发育和维持的。此外,我们通过回顾最近的研究结果,深入探讨了对共生微生物和食物抗原免疫反应的复杂性,强调了塑造免疫耐受的免疫背景。了解这些机制有助于我们理解免疫耐受是如何建立和维持的,为管理因对外来抗原免疫耐受丧失而导致的慢性炎症性疾病的潜在治疗方法提供见解。[《BMB报告》2025年;58(4):158 - 168]

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/142d/12041928/317775f2c711/bmb-58-4-158-f1.jpg

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