在患有多发性硬化症的患者免疫乱后,肠道微生物组与宿主关系的改变
Vinod K Gupta1, Guneet S Janda2, Heather K Pump3
1Microbiomics Program, Center for Individualized Medicine, Mayo Clinic, Rochester, MN.
Neurology(R) neuroimmunology & neuroinflammation
|January 17, 2025
概括
新诊断的多发性硬化症 (MS) 患者表现出改变的肠道细菌-IgA结合. B细胞枯竭疗法部分恢复了这些微生物模式,突出了肠道微生物组在MS中的作用.
科学领域:
- 免疫学 免疫学 免疫学
- 微生物学 微生物学
- 神经科学是一个神经科学.
背景情况:
- 肠道微生物共生体影响自身免疫力,通过微生物-IgA接口与多发性硬化症 (MS) 病理生理学的新兴联系.
- 在MS患者中观察到分泌IgA的B细胞和改变的肠道细菌-IgA结合,但宿主免疫反应,特别是B细胞枯竭,尚未得到充分研究.
研究的目的:
- 通过使用长读测序,评估在基线和B细胞枯竭后新诊断的MS患者的肠道微生物组组成.
- 通过评估微生物/免疫球蛋白A (IgA) 关系来研究宿主/微生物群相互作用.
主要方法:
- 从43名新诊断的,未经治疗的多发性硬化症患者和42名健康对照组收集的便样本.
- 19名多发性硬化症患者提供了6个月抗CD20治疗后的样本.
- 细菌流细胞测量和长时间读取的16S rRNA基因测序分析了宿主-微生物接口,免疫涂层得分比较IgA涂层与未涂层细菌.
主要成果:
- 与对照组相比,未经治疗的多发性硬化症患者显示IgA结合的便微生物群减少.
- 在总和IgA涂层分量中观察到显著的菌株级肠道细菌变化 (ASV).
- 具体的变化包括在MS中减少*Faecalibacterium prausnitzii*和增加*Monoglobus pectinyliticus*;在治疗后正常化IgA涂层的*Akkermansia muciniphila*.
结论:
- 对肠道微生物ASVs的分析揭示了MS中免疫调节引起的分类学菌株转移.
- 这些发现突出了肠道微生物群,IgA和宿主免疫系统在MS病原和治疗反应中的动态相互作用.
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