Scavenger receptor-A is a biomarker and effector of rheumatoid arthritis: A large-scale multicenter study

Early diagnosis is critical to improve outcomes in rheumatoid arthritis (RA), but current diagnostic tools have limited sensitivity. Here we report a large-scale multicenter study involving training and validation cohorts of 3,262 participants. We show that serum levels of soluble scavenger receptor...

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Veröffentlicht in:Nature communications 2020-04, Vol.11 (1), p.1911-1911, Article 1911
Hauptverfasser: Hu, Fanlei, Jiang, Xiang, Guo, Chunqing, Li, Yingni, Chen, Shixian, Zhang, Wei, Du, Yan, Wang, Ping, Zheng, Xi, Fang, Xiangyu, Li, Xin, Song, Jing, Xie, Yang, Huang, Fei, Xue, Jimeng, Bai, Mingxin, Jia, Yuan, Liu, Xu, Ren, Limin, Zhang, Xiaoying, Guo, Jianping, Pan, Hudan, Su, Yin, Yi, Huanfa, Ye, Hua, Zuo, Daming, Li, Juan, Wu, Huaxiang, Wang, Yongfu, Li, Ru, Liu, Liang, Wang, Xiang-Yang, Li, Zhanguo
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Sprache:eng
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Zusammenfassung:Early diagnosis is critical to improve outcomes in rheumatoid arthritis (RA), but current diagnostic tools have limited sensitivity. Here we report a large-scale multicenter study involving training and validation cohorts of 3,262 participants. We show that serum levels of soluble scavenger receptor-A (sSR-A) are increased in patients with RA and correlate positively with clinical and immunological features of the disease. This discriminatory capacity of sSR-A is clinically valuable and complements the diagnosis for early stage and seronegative RA. sSR-A also has 15.97% prevalence in undifferentiated arthritis patients. Furthermore, administration of SR-A accelerates the onset of experimental arthritis in mice, whereas inhibition of SR-A ameliorates the disease pathogenesis. Together, these data identify sSR-A as a potential biomarker in diagnosis of RA, and targeting SR-A might be a therapeutic strategy. Scavenger receptor-A (SR-A) is mostly expressed by myeloid cells and has been attributed a variety of biological functions. Here the authors assess SR-A as a biomarker for diagnosis of rheumatoid arthritis (RA) using large-scale training and validation cohorts and show that modulating SR-A levels can alter progression of collagen-induced arthritis in mice.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-020-15700-3