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老朋友假说:进化、免疫调节与必需的微生物输入

The old friends hypothesis: evolution, immunoregulation and essential microbial inputs.

作者信息

Rook Graham A W

机构信息

Centre for Clinical Microbiology, Department of Infection, UCL (University College London), London, United Kingdom.

出版信息

Front Allergy. 2023 Sep 12;4:1220481. doi: 10.3389/falgy.2023.1220481. eCollection 2023.

Abstract

In wealthy urbanised societies there have been striking increases in chronic inflammatory disorders such as allergies, autoimmunity and inflammatory bowel diseases. There has also been an increase in the prevalence of individuals with systemically raised levels of inflammatory biomarkers correlating with increased risk of metabolic, cardiovascular and psychiatric problems. These changing disease patterns indicate a broad failure of the mechanisms that should stop the immune system from attacking harmless allergens, components of self or gut contents, and that should terminate inappropriate inflammation. The Old Friends Hypothesis postulates that this broad failure of immunoregulation is due to inadequate exposures to the microorganisms that drive development of the immune system, and drive the expansion of components such as regulatory T cells (Treg) that mediate immunoregulatory mechanisms. An evolutionary approach helps us to identify the organisms on which we are in a state of evolved dependence for this function (Old Friends). The bottom line is that most of the organisms that drive the regulatory arm of the immune system come from our mothers and family and from the natural environment (including animals) and many of these organisms are symbiotic components of a healthy microbiota. Lifestyle changes that are interrupting our exposure to these organisms can now be identified, and many are closely associated with low socioeconomic status (SES) in wealthy countries. These insights will facilitate the development of education, diets and urban planning that can correct the immunoregulatory deficit, while simultaneously reducing other contributory factors such as epithelial damage.

摘要

在富裕的城市化社会中,诸如过敏、自身免疫性疾病和炎症性肠病等慢性炎症性疾病显著增加。系统性炎症生物标志物水平升高的个体患病率也有所增加,这些个体患代谢、心血管和精神疾病的风险也相应增加。这些不断变化的疾病模式表明,阻止免疫系统攻击无害过敏原、自身成分或肠道内容物,并终止不适当炎症的机制普遍失效。“老朋友假说”假定,这种免疫调节的普遍失效是由于对驱动免疫系统发育以及介导免疫调节机制的调节性T细胞(Treg)等成分扩增的微生物接触不足。一种进化方法有助于我们识别出在这一功能上(老朋友)我们处于进化依赖状态的生物体。关键在于,驱动免疫系统调节臂的大多数生物体来自我们的母亲和家庭,以及自然环境(包括动物),其中许多生物体是健康微生物群的共生成分。现在可以确定正在干扰我们接触这些生物体的生活方式变化,其中许多变化与富裕国家的低社会经济地位(SES)密切相关。这些见解将促进教育、饮食和城市规划的发展,从而纠正免疫调节缺陷,同时减少其他促成因素,如上皮损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c0/10524266/3a3074370f7b/falgy-04-1220481-g001.jpg

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