Miller Frederick W
National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina.
Arthritis Care Res (Hoboken). 2025 Jan;77(1):3-11. doi: 10.1002/acr.25423. Epub 2024 Sep 27.
A critical unanswered question is what is causing the increase in the prevalence of autoimmunity and autoimmune diseases around the world. Given the rapidity of change, this is likely the result of major recent alterations in our exposures to environmental risk factors for these diseases. More evidence is becoming available that the evolution of autoimmune disease, years or even decades in the making, results from multiple exposures that alter susceptible genomes and immune systems over time. Exposures during sensitive phases in key developmental or hormonal periods may set the stage for the effects of later exposures. It is likely that synergistic and additive impacts of exposure mixtures result in chronic low-level inflammation. This inflammation may eventually pass thresholds that lead to immune system activation and autoimmunity, and with further molecular and pathologic changes, the complete clinical syndrome emerges. Much work remains to be done to define the mechanisms and risk and protective factors for autoimmune conditions. However, evidence points to a variety of pollutants, xenobiotics, infections, occupational exposures, medications, smoking, psychosocial stressors, changes in diet, obesity, exercise, and sleep patterns, as well as climate change impacts of increased heat, storms, floods, wildfires, droughts, UV radiation, malnutrition, and changing infections, as possible contributors. Substantial investments in defining the role of causal factors, in whom and when their effects are most important, the necessary and sufficient gene-environment interactions, improved diagnostics and therapies, and preventive strategies are needed now to limit the many negative personal, societal, and financial impacts that will otherwise occur.
一个关键的未解决问题是,是什么导致了全球自身免疫性疾病和自身免疫病患病率的上升。鉴于变化的迅速性,这很可能是近期我们接触这些疾病的环境风险因素发生重大改变的结果。越来越多的证据表明,自身免疫病的演变历经数年甚至数十年,是多种暴露随着时间推移改变易感基因组和免疫系统的结果。在关键发育或激素时期的敏感阶段的暴露可能为后期暴露的影响奠定基础。暴露混合物的协同和累加影响可能导致慢性低水平炎症。这种炎症最终可能超过导致免疫系统激活和自身免疫的阈值,随着进一步的分子和病理变化,完整的临床综合征就会出现。要确定自身免疫性疾病的发病机制、风险因素和保护因素,仍有许多工作要做。然而,有证据表明,各种污染物、外源性物质、感染、职业暴露、药物、吸烟、心理社会压力源、饮食变化、肥胖、运动和睡眠模式,以及高温、风暴、洪水、野火、干旱、紫外线辐射、营养不良和感染变化等气候变化影响都可能是致病因素。现在需要大量投入来确定因果因素的作用、其影响最重要的人群和时间、必要且充分的基因 - 环境相互作用、改进诊断和治疗方法以及预防策略,以限制否则将会出现的许多负面个人、社会和经济影响。