新生儿Fc受体阻断是血浆置换适应症疾病的新兴治疗方法。

IF 1.4 4区 医学 Q4 HEMATOLOGY
Muharrem Yunce MD, Nakul Katyal MD, Grace Fortes Monis MD, PhD, Srikanth Muppidi MD
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引用次数: 2

摘要

新生儿Fc受体(FcRn)阻断可能代表了一种类似于血浆交换(PLEX)的降低免疫球蛋白水平的机制,因此对单采医生具有广泛的意义。尽管只有efgartigimod在2021年12月获得了美国食品药品监督管理局对重症肌无力的批准,但目前正在对本综述中概述的一组不同的IgG抗体介导的神经和血液系统疾病进行多种FcRn疗法的试验。在这篇综述中,我们讨论了FcRn的作用机制,以及它在各种神经和非神经疾病中的潜在应用。此外,我们进一步比较了PLEX和FcRn阻断的动力学和不良事件。我们鼓励单采医生熟悉这类药物,以便更好地了解这两种疗法如何单独使用,或与其他疗法联合使用,因为FcRn拮抗剂和PLEX通过降低IgG水平和致病抗体来改善临床状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neonatal Fc receptor blockade as emerging therapy in diseases with plasma exchange indications

Neonatal Fc receptor (FcRn) blockade may represent a mechanism similar to plasma exchange (PLEX) in reducing immunoglobulin levels and thus have a broad implication for apheresis practitioners. Although only efgartigimod received FDA approval for myasthenia gravis in December 2021, multiple trials are currently underway with different FcRn therapies in a varied group of IgG antibody-mediated neurological and hematological disorders which are outlined in this review. In this review we discuss FcRn's mechanism of action, and its potential use in various neurological and non-neurological diseases. In addition, we further compare the kinetics and adverse events of PLEX and FcRn blockade. We encourage apheresis practitioners to be familiar with this class of drugs in order to better understand how these two therapies can be used either standalone, or in combination with other therapies as both FcRn antagonism and PLEX improve clinical state by reducing IgG levels and pathogenic antibodies.

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来源期刊
CiteScore
2.80
自引率
13.30%
发文量
70
审稿时长
>12 weeks
期刊介绍: The Journal of Clinical Apheresis publishes articles dealing with all aspects of hemapheresis. Articles welcomed for review include those reporting basic research and clinical applications of therapeutic plasma exchange, therapeutic cytapheresis, therapeutic absorption, blood component collection and transfusion, donor recruitment and safety, administration of hemapheresis centers, and innovative applications of hemapheresis technology. Experimental studies, clinical trials, case reports, and concise reviews will be welcomed.
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