Huss André, Bachhuber Franziska, Feraudet-Tarisse Cécile, Hiergeist Andreas, Tumani Hayrettin
Department of Neurology, University Hospital Ulm, 89081 Ulm, Germany.
CEA, INRAE, Medicines and Healthcare Technologies Department (DMTS), SPI, Paris-Saclay University, 91191 Gif-sur-Yvette, France.
Biomedicines. 2024 Jun 23;12(7):1392. doi: 10.3390/biomedicines12071392.
Recent research has suggested a link between multiple sclerosis and the gut microbiota. This prospective pilot study aimed to investigate the composition of the gut microbiota in MS patients, the presence of epsilon toxin in the serum of MS patients, and the influence of disease-modifying drugs (DMDs) on epsilon toxin levels and on the microbiota. Epsilon toxin levels in blood were investigated by two methods, a qualitative ELISA and a highly sensitive quantitative ELISA. Neither epsilon toxin nor antibodies against it were detected in the analyzed serum samples. 16S ribosomal RNA sequencing was applied to obtain insights into the composition of the gut microbiota of MS patients. No significant differences in the quantity, diversity, and the relative abundance of fecal microbiota were observed in the gut microbiota of MS patients receiving various DMDs, including teriflunomide, natalizumab, ocrelizumab, and fingolimod, or no therapy. The present study did not provide evidence supporting the hypothesis of a causal relationship between epsilon toxin and multiple sclerosis.
近期研究表明多发性硬化症与肠道微生物群之间存在联系。这项前瞻性试点研究旨在调查多发性硬化症患者肠道微生物群的组成、患者血清中是否存在ε毒素,以及疾病修正药物(DMDs)对ε毒素水平和微生物群的影响。通过两种方法研究血液中的ε毒素水平,一种是定性酶联免疫吸附测定(ELISA),另一种是高灵敏度定量ELISA。在所分析的血清样本中未检测到ε毒素及其抗体。应用16S核糖体RNA测序来深入了解多发性硬化症患者肠道微生物群的组成。在接受包括特立氟胺、那他珠单抗、奥瑞珠单抗和芬戈莫德在内的各种DMDs治疗或未接受治疗的多发性硬化症患者的肠道微生物群中,未观察到粪便微生物群在数量、多样性和相对丰度上的显著差异。本研究没有提供证据支持ε毒素与多发性硬化症之间存在因果关系的假设。