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临床血管化复合组织同种异体移植中新型贝利尤单抗的应用。

De novo belatacept in clinical vascularized composite allotransplantation.

机构信息

Department of Surgery, Duke University School of Medicine, Durham, NC, USA.

Department of Orthopaedics, Duke University School of Medicine, Durham, NC, USA.

出版信息

Am J Transplant. 2018 Jul;18(7):1804-1809. doi: 10.1111/ajt.14910. Epub 2018 Jun 9.

Abstract

Most immunosuppressive regimens used in clinical vascularized composite allotransplantation (VCA) have been calcineurin inhibitor (CNI)-based. As such, most recipients have experienced CNI-related side effects. Costimulation blockade, specifically CD28/B7 inhibition with belatacept, has emerged as a clinical replacement for CNI-based immunosuppression in kidney transplantation. We have previously shown that belatacept can be used as a centerpiece immunosuppressant for VCA in nonhuman primates, and subsequently reported successful conversion from a CNI-based regimen to a belatacept-based regimen after clinical hand transplantation. We now report on the case of a hand transplant recipient, whom we have successfully treated with a de novo belatacept-based regimen, transitioned to a CNI-free regimen. This case demonstrates that belatacept can provide sufficient prophylaxis from rejection without chronic CNI-associated side effects, a particularly important goal in nonlifesaving solid organ transplants such as VCA.

摘要

大多数用于临床血管化复合组织同种异体移植(VCA)的免疫抑制方案都是基于钙调磷酸酶抑制剂(CNI)的。因此,大多数受者都经历了 CNI 相关的副作用。共刺激阻断,特别是使用 belatacept 抑制 CD28/B7,已成为肾移植中替代基于 CNI 的免疫抑制的临床方法。我们之前已经表明,belatacept 可以作为非人灵长类动物 VCA 的中心免疫抑制剂,随后报道了在临床手部移植后从基于 CNI 的方案成功转换为基于 belatacept 的方案。我们现在报告了一名手部移植受者的病例,我们成功地用新的基于 belatacept 的方案治疗了该患者,并过渡到无 CNI 的方案。该病例表明,belatacept 可以在没有慢性 CNI 相关副作用的情况下提供充分的排斥预防,这在非挽救生命的实体器官移植(如 VCA)中是一个特别重要的目标。

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