Marazzato Massimiliano, Iannuccelli Cristina, Guzzo Maria Paola, Nencioni Lucia, Lucchino Bruno, Radocchia Giulia, Gioia Chiara, Bonfiglio Giulia, Neroni Bruna, Guerrieri Francesca, Pantanella Fabrizio, Garzoli Stefania, Vomero Marta, Barbati Cristiana, Di Franco Manuela, Schippa Serena
Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Early Arthritis Clinic, Department of Internal Medicine, Anesthesiology and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.
Front Med (Lausanne). 2022 Jul 8;9:921675. doi: 10.3389/fmed.2022.921675. eCollection 2022.
Rheumatoid Arthritis (RA) is a chronic systemic autoimmune disease. Modifications of gut microbiota seem to be associated with the disease, but the impact of gut microbiota on therapies' outcome remains unclear. A role of T cells in RA pathogenesis has been addressed, particularly on the Th17/Treg cells balance. Our study aimed to evaluate in early RA (ERA) patients compared to a control group, fecal gut microbiota composition, short-chain fatty acids concentrations, and the levels of circulating Th17/Treg and their own cytokines, before and after 3 months of standard treatment (Methotrexate (MTX) plus glucocorticoids). Fecal microbiota characterization was carried out on 19 ERA patients and 20 controls matched for sex and age. Significant decreased biodiversity levels, and a partition on the base of the microbiota composition, between the ERA patients at baseline compared to controls, were observed. The co-occurrent analysis of interactions revealed a characteristic clustered structure of the microbial network in controls that is lost in ERA patients where an altered connection between microbes and clinical parameters/metabolites has been reported. Microbial markers such as , Cristiansella massiliensis, and resulted significantly enriched in control group while the species Blautia gnavus emerged to be more abundant in ERA patients. Our results showed an alteration in Th17/Treg balance with higher Th17 levels and lower Treg levels in ERA group respect to control at baseline, those data improved after therapy. Treatment administration and the achievement of a low disease activity/remission appear to exert a positive pressure on the structure of intestinal microbiota with the consequent restoration of biodiversity, of the structure of microbial network, and of the abundance of taxa that became closer to those presented by the subject without the disease. We also found an association between Blautia gnavus and ERA patients characterized by a significant reduction of propionic acid level. Furthermore significant differences highlighted at baseline among controls and ERA patients are no more evident after treatment. These data corroborate the role played by gut microbiota in the disease and suggest that therapy aimed to restore gut microbiota would improve treatment outcome.
类风湿关节炎(RA)是一种慢性全身性自身免疫性疾病。肠道微生物群的改变似乎与该疾病有关,但肠道微生物群对治疗结果的影响仍不清楚。T细胞在RA发病机制中的作用已得到关注,特别是在Th17/Treg细胞平衡方面。我们的研究旨在评估早期RA(ERA)患者与对照组相比,在标准治疗(甲氨蝶呤(MTX)加糖皮质激素)3个月前后的粪便肠道微生物群组成、短链脂肪酸浓度以及循环Th17/Treg及其自身细胞因子的水平。对19例ERA患者和20例年龄和性别匹配的对照进行了粪便微生物群特征分析。与对照组相比,观察到ERA患者基线时生物多样性水平显著降低,且基于微生物群组成存在分类。相互作用的共现分析揭示了对照组中微生物网络的特征性聚类结构,而在ERA患者中这种结构消失,据报道ERA患者中微生物与临床参数/代谢物之间的连接发生了改变。诸如马赛克里斯蒂安菌等微生物标志物在对照组中显著富集,而在ERA患者中格氏布劳特菌更为丰富。我们的结果显示,与基线时的对照组相比,ERA组Th17/Treg平衡发生改变,Th17水平较高而Treg水平较低,治疗后这些数据有所改善。治疗的实施以及低疾病活动度/缓解的实现似乎对肠道微生物群结构产生了积极影响,从而恢复了生物多样性、微生物网络结构以及分类群的丰度,使其更接近无病受试者的情况。我们还发现格氏布劳特菌与ERA患者之间存在关联,其特征是丙酸水平显著降低。此外,治疗后对照组和ERA患者基线时突出的显著差异不再明显。这些数据证实了肠道微生物群在该疾病中的作用,并表明旨在恢复肠道微生物群的治疗将改善治疗结果。