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补体系统作为造血干细胞移植相关血栓性微血管病的新靶点

Complement System as a New Target for Hematopoietic Stem Cell Transplantation-Related Thrombotic Microangiopathy.

作者信息

Ardissino Gianluigi, Capone Valentina, Tedeschi Silvana, Porcaro Luigi, Cugno Massimo

机构信息

Center for HUS Prevention, Control and Management at Pediatric Nephrology, Dialysis and Transplant Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milano, Italy.

Medical Genetics Laboratory, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milano, Italy.

出版信息

Pharmaceuticals (Basel). 2022 Jul 9;15(7):845. doi: 10.3390/ph15070845.

Abstract

Thrombotic microangiopathy (TMA) is a complication that may occur after autologous or allogeneic hematopoietic stem cell transplantation (HSCT) and is conventionally called transplant-associated thrombotic microangiopathy (TA-TMA). Despite the many efforts made to understand the mechanisms of TA-TMA, its pathogenesis is largely unknown, its diagnosis is challenging and the case-fatality rate remains high. The hallmarks of TA-TMA, as for any TMA, are platelet consumption, hemolysis, and organ dysfunction, particularly the kidney, leading also to hypertension. However, coexisting complications, such as infections and/or immune-mediated injury and/or drug toxicity, together with the heterogeneity of diagnostic criteria, render the diagnosis difficult. During the last 10 years, evidence has been provided on the involvement of the complement system in the pathophysiology of TA-TMA, supported by functional, genetic, and therapeutic data. Complement dysregulation is believed to collaborate with other proinflammatory and procoagulant factors to cause endothelial injury and consequent microvascular thrombosis and tissue damage. However, data on complement activation in TA-TMA are not sufficient to support a systematic use of complement inhibition therapy in all patients. Thus, it seems reasonable to propose complement inhibition therapy only to those patients exhibiting a clear complement activation according to the available biomarkers. Several agents are now available to inhibit complement activity: two drugs have been successfully used in TA-TMA, particularly in pediatric cases (eculizumab and narsoplimab) and others are at different stages of development (ravulizumab, coversin, pegcetacoplan, crovalimab, avacopan, iptacopan, danicopan, BCX9930, and AMY-101).

摘要

血栓性微血管病(TMA)是自体或异基因造血干细胞移植(HSCT)后可能发生的一种并发症,传统上称为移植相关血栓性微血管病(TA-TMA)。尽管人们为了解TA-TMA的发病机制付出了诸多努力,但其发病机制在很大程度上仍不清楚,诊断具有挑战性,病死率仍然很高。与任何TMA一样,TA-TMA的特征是血小板消耗、溶血和器官功能障碍,尤其是肾脏,还会导致高血压。然而,诸如感染和/或免疫介导损伤和/或药物毒性等并存并发症,以及诊断标准的异质性,使得诊断变得困难。在过去10年中,功能、基因和治疗数据支持了补体系统参与TA-TMA病理生理学的证据。补体失调被认为与其他促炎和促凝因子共同作用,导致内皮损伤,进而引起微血管血栓形成和组织损伤。然而,TA-TMA中补体激活的数据不足以支持在所有患者中系统使用补体抑制疗法。因此,仅对那些根据现有生物标志物显示出明确补体激活的患者提出补体抑制疗法似乎是合理的。目前有几种药物可用于抑制补体活性:两种药物已成功用于TA-TMA,特别是在儿科病例中(依库珠单抗和那索普单抗),其他药物正处于不同的开发阶段(ravulizumab、coversin、pegcetacoplan、crovalimab、avacopan、iptacopan、danicopan、BCX9930和AMY-101)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8286/9325021/c2b8d6d61d0d/pharmaceuticals-15-00845-g001.jpg

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