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Gut microbiota and rheumatoid arthritis: From pathogenesis to novel therapeutic opportunities
被引:126
作者:
Zhao, Ting
[1
,2
]
Wei, Yuanyuan
[1
]
Zhu, Youyang
[3
]
Xie, Zhaohu
[1
]
Hai, Qingshan
[1
]
Li, Zhaofu
[1
]
Qin, Dongdong
[1
]
机构:
[1] Yunnan Univ Chinese Med, Sch Basic Med Sci, Kunming, Peoples R China
[2] Yunnan Univ Chinese Med, Sch Clin Med 1, Kunming, Peoples R China
[3] Yunnan Univ Chinese Med, Affiliated Hosp 3, Kunming, Peoples R China
基金:
中国国家自然科学基金;
关键词:
rheumatoid arthritis;
gut microbiota;
immune response;
inflammation;
drug treatment;
T-CELLS;
LACTOBACILLUS-CASEI;
FECAL MICROBIOTA;
SULFASALAZINE;
METABOLISM;
ACTIVATION;
COMMENSAL;
RESPONSES;
PATHWAY;
HEALTH;
D O I:
10.3389/fimmu.2022.1007165
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Rheumatoid arthritis (RA) is a chronic autoimmune disease that primarily affects the joints. Microbial infection is considered a crucial inducer of RA. Alterations in the composition of intestinal bacteria in individuals with preclinical and established RA suggest a vital role of the gut microbiota in immune dysfunction characteristic of RA. However, the mechanisms by which gut dysbiosis contributes to RA are not fully understood. Furthermore, multiple therapies commonly used to treat RA may alter gut microbiota diversity, suggesting that modulating the gut microbiota may help prevent or treat RA. Hence, a better understanding of the changes in the gut microbiota that accompany RA should aid the development of novel therapeutic approaches. This mini-review discusses the impact of gut dysbiosis in the pathogenesis of RA, the selection of gut microbiota-related biomarkers for diagnosing RA, and provides examples of cross-modulation between the gut microbiota and some drugs commonly used to treat RA. Some suggestions and outlooks are also raised, which may help guide future research efforts.
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页数:8
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