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Correlation of Professional Antigen-Presenting Tbet+CD11c+ B Cells With Bone Destruction in Untreated Rheumatoid Arthritis
Arthritis & Rheumatology ( IF 13.3 ) Pub Date : 2024-04-03 , DOI: 10.1002/art.42857
Sarah McGrath 1 , Kristoffer Grimstad 1, 2 , Katrin Thorarinsdottir 1 , Kristina Forslind 3, 4 , Daniel Glinatsi 5 , Monica Leu Agelii 1 , Alaitz Aranburu 1 , Timothy Sundell 1 , Charlotte A. Jonsson 1 , Alessandro Camponeschi 1 , Anna‐Karin Hultgård Ekwall 1, 6 , Andreas Tilevik 2 , Inger Gjertsson 1, 6 , Inga‐Lill Mårtensson 1
Affiliation  

Subsets of CD21−/low memory B cells (MBCs), including double-negative (DN, CD27IgD) and Tbet+CD11c+ cells, are expanded in chronic inflammatory diseases. In rheumatoid arthritis (RA), CD21−/low MBCs correlate with joint destruction. However, whether this is due to the Tbet+CD11c+ subset, its function and pathogenic contribution to RA are unknown. This study aims to investigate the association between CD21−/lowTbet+CD11c+ MBCs and joint destruction as well as other clinical parameters and to elucidate their functional properties in patients with untreated RA (uRA).

中文翻译:


专业抗原呈递 Tbet+CD11c+ B 细胞与未经治疗的类风湿性关节炎骨破坏的相关性



CD21 −/low 记忆 B 细胞 (MBC) 子集,包括双阴性(DN、CD27 IgD )和 Tbet + CD11c + 细胞在慢性炎症性疾病中扩增。在类风湿性关节炎 (RA) 中,CD21 −/low MBC 与关节破坏相关。然而,这是否是由于 Tbet + CD11c + 子集所致,其功能和对 RA 的致病作用尚不清楚。本研究旨在调查 CD21 −/low Tbet + CD11c + MBC 与关节破坏以及其他临床参数之间的关联,并阐明其在患者中的功能特性患有未经治疗的 RA (uRA)。
更新日期:2024-04-03
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