生物钟:自身免疫性疾病的免疫调节因子

IF 2.7 4区 医学 Q3 IMMUNOLOGY
Ye-Jun Wu, Shu-Ying Zhang, Hong-Yu Chen, Xin-Ran He, Guang-Rui Yang
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引用次数: 0

摘要

自身免疫性疾病的特点是免疫系统错误地攻击人体自身组织,这是一个日益受到全球关注的问题,发病率越来越高。生物钟是生理过程的基本调节器,对免疫功能起着关键的调节作用。这篇综述探讨了自身免疫发病机制中昼夜节律和免疫反应之间的复杂联系,以及破坏如何加剧疾病。方法:本文综合分析了免疫功能(白细胞运输、细胞因子分泌、吞噬)和自身免疫进展的昼夜节律调节的最新研究。关键证据包括核心时钟蛋白的作用,如脑和肌肉arnt样1 (BMAL1)、昼夜运动输出周期衰竭(clock)和rev - erba,以及昼夜调节的免疫细胞,以及环境/生活方式诱导的昼夜节律中断的影响。结果:昼夜节律显著影响自身免疫性疾病的进展和症状模式(例如,类风湿关节炎的早晨关节僵硬)。核心时钟蛋白和节律性免疫细胞对体内平衡至关重要。昼夜节律紊乱加剧免疫功能紊乱,促进慢性炎症和自身免疫。结论生物钟是免疫功能和自身免疫发病机制的重要调节因子。破坏使疾病恶化。了解这些机制为治疗干预开辟了新的途径,包括时间疗法和靶向时钟基因,有可能改善自身免疫性疾病的治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Circadian Clock: A Regulator of Immunity in Autoimmune Diseases

Circadian Clock: A Regulator of Immunity in Autoimmune Diseases

Aim

Autoimmune diseases, characterized by the immune system mistakenly attacking the body's own tissues, are a growing global concern, with increasing prevalence. The circadian clock is a fundamental regulator of physiological processes, critically modulating immune functions. This review explores the intricate connections between circadian rhythms and immune responses in autoimmune pathogenesis and how disruptions exacerbate disease.

Methods

This synthesis examines recent research on circadian regulation of immune functions (leukocyte trafficking, cytokine secreion, phagocytosis) and autoimmune progression. Key evidence includes roles of core clock proteins such as brain and muscle ARNT-Like 1 (BMAL1), circadian locomotor output cycles kaput (CLOCK), and REV-ERBα, along with circadian-regulated immune cells, and impacts of environmental/lifestyle-induced circadian disruption.

Results

Ciradian rhythms significantly influence autoimmune disease progression and symptom patterns (e.g., morning joint stiffness in rheumatoid arthritis). Core clock proteins and rhythmic immune cells are critical for homeostasis. Circadian disruptions exacerbate immune dysfunction, promoting chronic inflammation and autoimmunity.

Conclusions

The circadian clock is a fundamental regulator of immune function and autoimmune pathogenesis. Disruption worsens disease progression. Understanding these mechanisms opens new avenues for therapeutic interventions, including chronotherapy and targeting clock genes, with the potential to improve treatment outcomes in autoimmune diseases.

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来源期刊
Immunity, Inflammation and Disease
Immunity, Inflammation and Disease Medicine-Immunology and Allergy
CiteScore
3.60
自引率
0.00%
发文量
146
审稿时长
8 weeks
期刊介绍: Immunity, Inflammation and Disease is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research across the broad field of immunology. Immunity, Inflammation and Disease gives rapid consideration to papers in all areas of clinical and basic research. The journal is indexed in Medline and the Science Citation Index Expanded (part of Web of Science), among others. It welcomes original work that enhances the understanding of immunology in areas including: • cellular and molecular immunology • clinical immunology • allergy • immunochemistry • immunogenetics • immune signalling • immune development • imaging • mathematical modelling • autoimmunity • transplantation immunology • cancer immunology
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