抗肿瘤坏死因子药物对脊柱关节炎、类风湿性关节炎和炎症性肠病患者肠道微生物群的影响。

Rheumatology and immunology research Pub Date : 2024-03-31 eCollection Date: 2024-03-01 DOI:10.1515/rir-2024-0003
Francesco Ciccia, Nikolas Konstantine Dussias, Saviana Gandolfo, Fernando Rizzello, Paolo Gionchetti
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引用次数: 0

摘要

脊柱关节炎(Spondyloarthritis,SPA)、类风湿性关节炎(Rheumatoid arthritis,RA)和炎症性肠病(Inflammatory bowel diseases,IBD)都是慢性炎症性自身免疫性疾病,与肠道微生物群组成的改变(即菌群失调)有关。就 SpA 和 RA 而言,肠道-关节-假体轴是一种假设,最近的数据表明,菌群失调可能直接导致关节和脊柱炎症的发生和延续。以肿瘤坏死因子(TNF)为靶点的生物药物可有效治疗这些疾病,并已证明可部分恢复紊乱的微生物群。因此,同时影响这些疾病的肠道和关节部分的药物,如抗 TNF 药物,可能会作用于肠道微生物群。然而,尽管抗肿瘤坏死因子-α疗法疗效显著,但无应答者屡见不鲜,而且患者预后的预测因素尚未确定。在这篇叙述性综述中,我们总结了抗肿瘤坏死因子药物对 SpA、RA 和 IBD 患者肠道微生物群下游效应的最新研究。我们还讨论了这些变化是否可作为抗肿瘤坏死因子反应的预测性生物标志物。
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The effect of anti-TNF drugs on the intestinal microbiota in patients with spondyloarthritis, rheumatoid arthritis, and inflammatory bowel diseases.

Spondyloarthritis (SpA), rheumatoid arthritis (RA), and inflammatory bowel diseases (IBD) are chronic inflammatory autoimmune diseases that are associated with alterations in the composition of the intestinal microbiota (i.e., dysbiosis). For SpA and RA, a gut-joint-enthesis axis is hypothesized and recent data suggests that dysbiosis may contribute directly to initiating and perpetuating joint and spine inflammation. Biologic drugs targeting tumor necrosis factor (TNF) are effective in treating these diseases and have been shown to partially restore the disrupted microbiome. Hence, drugs that affect both the intestinal and joint components of these diseases, such as anti-TNF drugs, may act on the intestinal microbiome. However, despite the remarkable efficacy of anti-TNF-α treatments, non-responders are frequent, and predictors of patient outcomes have not been identified. In this narrative review, we summarize recent research on the downstream effects of anti-TNF drugs on the intestinal microbiota in SpA, RA, and IBD. We also discuss whether these changes could have a role as predictive biomarkers of anti-TNF response.

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