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B cells identified according to their expression of CD19 and surface ig are depleted from peripheral blood by rituximab in patients with rheumatoid arthritis: Comment on the article by Jones et al

机译:类风湿关节炎患者根据利他昔单抗从CD19和表面ig的表达中鉴定出的B细胞已从外周血中耗竭:评论Jones等人的文章

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摘要

We read with great interest the report by Jones et al (1), wherein they described the expression of CD19 by human B cells during in vitro incubation of peripheral blood mono-nuclear cells (PBMCs) with rituximab (RTX), the B cell-depleting anti-CD20 monoclonal antibody approved for treatment of rheumatoid arthritis (RA) and non-Hodgkin's lymphoma. The authors reported not only the loss of CD19-expressing cells in these cultures, but also the reduction of CD19 expression levels in individual cells after coincubation with RTX. They therefore suggested that the application of CD19 as a marker to monitor B cell depletion in vivo might be compromised by RTX, and that studies relying on the quantification of CD 19+ cells may overestimate the degree of actual B cell depletion.
机译:我们非常感兴趣地阅读了Jones等(1)的报告,其中他们描述了人B细胞与利妥昔单抗(RTX)体外孵育外周血单核细胞(PBMC)时CD19的表达,耗竭的抗CD20单克隆抗体,已批准用于治疗类风湿关节炎(RA)和非霍奇金淋巴瘤。作者不仅报道了这些培养物中表达CD19的细胞的损失,还报道了与RTX共孵育后单个细胞中CD19表达水平的降低。因此,他们建议RTX可能会损害CD19作为标记物在体内监测B细胞枯竭的应用,而依赖CD 19+细胞定量的研究可能会高估实际B细胞枯竭的程度。

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