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Aberrant B cells, autoimmunity and the benefit of targeting B cells in chronic graft-versus-host disease.
Autoimmunity Reviews ( IF 9.2 ) Pub Date : 2020-02-13 , DOI: 10.1016/j.autrev.2020.102493
Dana Yehudai-Ofir 1 , Israel Henig 1 , Tsila Zuckerman 2
Affiliation  

Chronic graft-versus-host disease (cGVHD) remains the main complication of allogeneic hematopoietic stem cell transplantation, limiting its chances for a successful outcome. The over-activity of CD4+ effector T cells and the excessive production of pro-inflammatory cytokines are followed by the development of immune-mediated inflammation and fibrosis of multiple organs. This is the reason for adopting T cell targeting therapies such as cyclosporine A, tacrolimus and mycophenolate mofetil. However, 40% of treated cGVHD patients remain unresponsive, which results in increased morbidity and mortality. Given the complexity of cGVHD pathogenesis, the involvement of B cells as an important player also needs to be explored. Function of aberrant B cells and secretion of relevant cytokines such as B cell activating factor (BAFF) have been found to correlate with cGVHD severity and have therefore become therapeutic targets. Better understanding of the role of B cells and their efficient targeting could improve the outcome of cGVHD.

中文翻译:

慢性移植物抗宿主病中异常B细胞,自身免疫和靶向B细胞的益处。

慢性移植物抗宿主病(cGVHD)仍然是同种异体造血干细胞移植的主要并发症,限制了其获得成功结果的机会。CD4 +效应T细胞的过度活性和促炎性细胞因子的过度产生,随后是免疫介导的炎症和多器官纤维化的发展。这就是采用靶向T细胞疗法(例如环孢霉素A,他克莫司和霉酚酸酯)的原因。但是,接受治疗的cGVHD患者中有40%仍然无反应,这导致发病率和死亡率增加。鉴于cGVHD发病机制的复杂性,还需要探索B细胞作为重要参与者的参与。已经发现异常B细胞的功能和相关细胞因子例如B细胞活化因子(BAFF)的分泌与cGVHD严重程度相关,因此已成为治疗靶标。更好地了解B细胞的作用及其有效靶向可以改善cGVHD的结果。
更新日期:2020-02-20
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