CD32 (Fc γ RIIB) expression is low on CD21 low B cells from systemic sclerosis patients with digital ulcers, interstitial lung disease, and anti-topoisomerase I autoantibodies

被引:1
|
作者
Kourkouni, Evangeli [1 ]
Tsiogkas, Sotirios G. [1 ]
Mavropoulos, Athanasios [1 ]
Simopoulou, Theodora [1 ]
Katsiari, Christina G. [1 ]
Bogdanos, Dimitrios P. [1 ]
Sakkas, Lazaros I. [1 ,2 ]
机构
[1] Univ Thessaly, Fac Med, Sch Hlth Sci, Dept Rheumatol & Clin Immunol, Larisa, Greece
[2] IASO Thessalias Gen Hosp, Larisa, Greece
关键词
Autoreactive B cells; Anti-topoisomerase I autoantibody; Fc gamma RIIB; Interstitial lung disease; Microvasculopathy; Systemic sclerosis; AUTOREACTIVITY; POPULATION; CRITERIA;
D O I
10.1016/j.clim.2024.110195
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD21 low B cells have recently been found increased in SSc-associated digital ulcers (DUs) or interstitial lung disease (ILD). To further characterize CD21 low B cells which encompass autoreactive cells, we analyzed their expression of the inhibitory CD32 receptor in SSc. Peripheral blood mononuclear cells from 27 patients with SSc and 15 age -and sex-matched healthy controls (HCs) were analyzed with multicolor flow cytometry. CD21 low B cells were significantly increased in patients with DUs (51.3%) compared to HCs (28.1%) and in patients with ILD (53.1%) compared to HCs. CD21 low CD32 low B cells were significantly increased in patients with DUs (23.8%) compared to HCs (4.4%), in patients with ILD (28.4%) compared to HCs, and in anti-topoisomerase I (+) patients (21.5%) compared to HCs and to anti-topoisomerase I (-) patients (2.4%). Autoreactive B cells recognizing Topoisomerase I were predominantly within CD32 low cell fraction. Our study further supports the autoreactive status of CD21 low CD32 low B cells in SSc patients.
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页数:4
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