Department of Chemistry, University of Connecticut , Storrs, CT, USA.
Department of Oral Health and Diagnostic Sciences, University of Connecticut School of Dental Medicine , Farmington, CT, USA.
Clin Transl Immunology. 2013 Nov 15;2(11):e8. doi: 10.1038/cti.2013.11. eCollection 2013 Nov.
Multiple sclerosis (MS) is an autoimmune disease of unknown etiology. Infectious agents have been suggested to have a role as environmental factors in MS, but this concept remains controversial. Recently, gastrointestinal commensal bacteria have been implicated in the pathogenesis of autoimmune diseases, but mechanisms underlying the relationship of human systemic autoimmunity with the commensal microbiome have yet to be identified. Consistent with the lack of understanding of pathogenic mechanisms and relevant environmental factors in MS, no blood biomarkers have been identified that distinguish MS patients from healthy individuals. We recently identified a unique gastrointestinal and oral bacteria-derived lipodipeptide, Lipid 654, which is produced by commensal bacteria and functions as a human and mouse Toll-like receptor 2 ligand. Using multiple-reaction-monitoring mass spectrometry, a critical approach in targeted lipidomics, we now report that Lipid 654 can be recovered in the serum of healthy individuals. Most interestingly, we find that Lipid 654 is expressed at significantly lower levels in the serum of patients with MS compared with both healthy individuals and patients with Alzheimer's disease. These results thus identify for the first time a potential mechanism relating the gastrointestinal and oral commensal microbiome to a human systemic autoimmune disease. In addition, these results also identify a potential etiologic environmental factor and novel clinically relevant serum biomarker for MS.
多发性硬化症(MS)是一种病因不明的自身免疫性疾病。有研究提示传染性病原体可能在 MS 的发病环境因素中起作用,但这一概念仍存在争议。最近,胃肠道共生细菌被认为与自身免疫性疾病的发病机制有关,但人类系统性自身免疫与共生微生物组之间的关系的机制尚未确定。与对 MS 的发病机制和相关环境因素缺乏了解一致的是,尚未发现能够将 MS 患者与健康个体区分开来的血液生物标志物。我们最近发现了一种独特的胃肠道和口腔共生细菌衍生的脂肽 Lipid 654,它由共生细菌产生,作为人类和小鼠 Toll 样受体 2 的配体发挥作用。使用多重反应监测质谱法(靶向脂质组学的关键方法),我们现在报告说,Lipid 654 可以在健康个体的血清中被回收。最有趣的是,我们发现与健康个体和阿尔茨海默病患者相比,MS 患者的血清中 Lipid 654 的表达水平显著降低。这些结果首次确定了将胃肠道和口腔共生微生物组与人类系统性自身免疫性疾病相关联的潜在机制。此外,这些结果还确定了 MS 的潜在病因环境因素和新的临床相关血清生物标志物。