0
Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Sign in to save

The exposome-autoimmunity axis: environmental xenobiotics, gut dysbiosis, and potential pathways to immunosenescence

Food and Chemical Toxicology 2026
Ferhat Osman Daşdemir, Mehmet Ferhat Sari, Buket AKTAŞ, Bekir Kocazeybek

Summary

This review pulls together existing research suggesting that everyday pollutants, like microplastics, air pollution, pesticides, and heavy metals, may disrupt your gut bacteria and immune system in ways that speed up immune "aging" and increase the risk of autoimmune diseases. The proposed chain reaction: pollutants damage your gut lining, throw off the balance of gut bacteria, and trigger inflammation that can wear down immune cells faster than normal, potentially making the body more likely to attack itself. That said, the authors caution that much of this evidence comes from lab studies using pollutant levels much higher than what people typ

Body Systems
Models
Study Type In vivo

The escalating incidence of autoimmune diseases cannot be fully explained by genetics alone. It is increasingly linked to the exposome-the cumulative burden of lifelong environmental exposures. This review examines how pollutants (particulate matter, microplastics, agrochemicals, heavy metals) reshape the gut microbiota-immune axis and disrupt intestinal homeostasis. This triggers profound dysbiosis, characterized by reduced commensal diversity and expanded pathobionts. We highlight three mechanisms driving pollution-induced immune reprogramming: (i) barrier compromise facilitating metabolic endotoxemia; (ii) toxic Aryl Hydrocarbon Receptor (AhR) overactivation skewing the Th17/Treg balance; and (iii) epigenetic modifications like aberrant DNA methylation. Chronic environmental exposure accelerates telomere attrition, inducing premature immunosenescence and inflammaging. This promotes the pathological accumulation of senescent T cells and Age-associated B Cells (ABCs), linking environmental stress to tissue damage and autoantibody generation. However, a major limitation of the current literature is that many in vivo and in vitro models employ supraphysiological concentrations of pollutants that do not reflect actual human exposure scenarios. Without evaluating these specific exposure scenarios against realistic human gut concentrations, it is difficult to determine under which exact conditions the postulated dysbiotic effects occur. Ultimately, mitigating environmental risks and employing microbiota-targeted therapeutics are vital to restore barrier integrity.

Share this paper