细胞生物学
B细胞
免疫系统
幼稚B细胞
树突状细胞
T细胞
细胞
化学
体外
抗体
抗原提呈细胞
B-1电池
生物
调节性B细胞
抗原
免疫学
抗原呈递
机制(生物学)
免疫耐受
记忆B细胞
多克隆B细胞反应
CD40
细胞生长
细胞分化
细胞培养
作者
Konstantina Morali,Juulke Steuten,Fabio Russo,Francesca Romana Santoni de Sio,Charlotte Menage,Valentina Consoli,Andrea Annoni,Silvia Iaia,S. Marieke van Ham,Anja ten Brinke,Silvia Gregori
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2025-11-21
卷期号:11 (47): eadu3624-eadu3624
标识
DOI:10.1126/sciadv.adu3624
摘要
B cells regulate immune responses via antibody production and antigen (Ag) presentation. Although B cell depletion is used therapeutically, it may be associated with side effects, highlighting the need for alternative B cell–targeted approaches. While tolerogenic dendritic cells (tolDC) are known to modulate T cell responses, their impact on B cells is poorly defined. We show that IL-10–producing tolDC (DC IL-10 ) regulate B cell responses through direct and indirect mechanisms. DC IL-10 enhances T cell–independent human B cell proliferation and differentiation while suppressing Ag-specific memory B cells via T cell inhibition in vitro and dampen Ag-specific IgG production in preclinical humanized and murine models. These findings reveal a dual mechanism by which DC IL-10 regulates B cell responses, broadening their application as a cell-based approach to treating immune-mediated diseases by targeting both B and T cells.
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