Center for Precision Medicine Research, Marshfield Clinic Research Institute, Marshfield, WI, United States.
Department of Neurology, Marshfield Clinic Health System, Marshfield, WI, United States.
Front Immunol. 2022 Aug 15;13:972160. doi: 10.3389/fimmu.2022.972160. eCollection 2022.
The etiological complexity of multiple sclerosis, an immune-mediated, neurodegenerative disease with multifactorial etiology is still elusive because of an incomplete understanding of the complex synergy between contributing factors such as genetic susceptibility and aberrant immune response. Recently, the disease phenotypes have also been shown to be associated with dysbiosis of the gut microbiome, a dynamic reservoir of billions of microbes, their proteins and metabolites capable of mimicring the autoantigens. Microbial factors could potentially trigger the neuroinflammation and symptoms of MS. In this perspective article, we discussed how microbial molecules resulting from a leaky gut might mimic a host's autoantigen, potentially contributing to the disease disequilibrium. It further highlights the importance of targeting the gut microbiome for alternate therapeutic options for the treatment of MS.
多发性硬化症是一种免疫介导的神经退行性疾病,病因复杂,由于我们对遗传易感性和异常免疫反应等多种因素之间复杂协同作用的理解还不完全,因此其病因仍然难以捉摸。最近,疾病表型也与肠道微生物组的失调有关,肠道微生物组是一个拥有数十亿微生物、其蛋白质和代谢物的动态储库,能够模拟自身抗原。微生物因素可能会引发神经炎症和多发性硬化症的症状。在这篇观点文章中,我们讨论了肠道通透性增加导致的微生物分子如何模拟宿主的自身抗原,从而可能导致疾病失衡。它进一步强调了针对肠道微生物组的重要性,为多发性硬化症的治疗提供了替代治疗选择。