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伊米苷酶在实体器官移植中的研究进展。

A review of imlifidase in solid organ transplantation.

机构信息

Vice Chair for Research, NYU Langone Health, Transplant Institute , New York, NY, USA.

出版信息

Expert Opin Biol Ther. 2021 Feb;21(2):135-143. doi: 10.1080/14712598.2021.1850685. Epub 2020 Dec 8.

Abstract

Sensitization to human leukocyte antigens has long posed an obstacle to organ transplantation. With desensitization protocol refinement, new drug development, and organ allocation policy changes, access to transplant for sensitized patients has never been greater. Yet in spite of these advances the problem of donor-specific antibody remains incompletely solved, and many patients remain poorly served by the therapies that do exist. Area covered: Imlifidase is a new drug with a mechanism of action that enables it to transiently yet efficiently eliminate donor-specific antibody over a much more rapid time course than any heretofore existing therapy. This unique property suggests that imlifidase may have far-reaching potential for patients in whom donor-specific antibodies may preclude successful transplantation. Below follows a review of the clinical experience with imlifidase to date as well as a discussion of the transplant applications that eagerly await the availability of this novel agent. Expert opinion: Imlifidase is a first-in-class pharmaceutical agent that safely and efficiently cleaves IgG, and holds promise to be a game-changer for sensitized patients in need of lifesaving organ transplants.

摘要

针对人类白细胞抗原的致敏作用长期以来一直是器官移植的障碍。随着脱敏方案的完善、新药的开发和器官分配政策的改变,致敏患者接受移植的机会从未如此之大。然而,尽管取得了这些进展,但供体特异性抗体的问题仍未得到完全解决,许多患者仍然无法从现有的治疗方法中得到很好的治疗。

涵盖领域

伊米苷酶是一种新药,其作用机制使其能够在比以往任何现有治疗方法都更短的时间内,有效地暂时消除供体特异性抗体。这种独特的特性表明,伊米苷酶可能对那些因供体特异性抗体而无法成功移植的患者具有深远的潜力。下文回顾了迄今为止伊米苷酶的临床经验,并讨论了急切等待这种新型药物的移植应用。

专家意见

伊米苷酶是一种首创的药物制剂,可安全有效地切割 IgG,并有望成为需要挽救生命的器官移植的致敏患者的游戏规则改变者。

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