Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Ancilia Biosciences, New York, NY 19808, USA.
Cell Host Microbe. 2021 May 12;29(5):726-739.e5. doi: 10.1016/j.chom.2021.03.020. Epub 2021 May 5.
Rheumatoid arthritis (RA) is an autoimmune disease characterized in seropositive individuals by the presence of anti-cyclic citrullinated protein (CCP) antibodies. RA is linked to the intestinal microbiota, yet the association of microbes with CCP serology and their contribution to RA is unclear. We describe intestinal phage communities of individuals at risk for developing RA, with or without anti-CCP antibodies, whose first-degree relatives have been diagnosed with RA. We show that at-risk individuals harbor intestinal phage compositions that diverge based on CCP serology, are dominated by Streptococcaceae, Bacteroidaceae, and Lachnospiraceae phages, and may originate from disparate ecosystems. These phages encode unique repertoires of auxiliary metabolic genes, which associate with anti-CCP status, suggesting that these phages directly influence the metabolic and immunomodulatory capability of the microbiota. This work sets the stage for the use of phages as preclinical biomarkers and provides insight into a possible microbial-based causation of RA disease development.
类风湿关节炎(RA)是一种自身免疫性疾病,在血清阳性个体中表现为存在抗环瓜氨酸肽(CCP)抗体。RA 与肠道微生物群有关,但微生物与 CCP 血清学的关联及其对 RA 的贡献尚不清楚。我们描述了患有或不患有抗 CCP 抗体的 RA 高危人群的肠道噬菌体群落,其一级亲属已被诊断患有 RA。我们表明,高危个体的肠道噬菌体组成因 CCP 血清学而不同,主要由链球菌科、拟杆菌科和lachnospiraceae 噬菌体主导,可能来自不同的生态系统。这些噬菌体编码独特的辅助代谢基因库,与抗 CCP 状态相关,表明这些噬菌体直接影响微生物群的代谢和免疫调节能力。这项工作为噬菌体作为临床前生物标志物的应用奠定了基础,并为 RA 疾病发展的可能微生物基础病因提供了新的见解。