Department of Surgery, Duke University School of Medicine, Durham, NC, USA.
Department of Orthopaedics, Duke University School of Medicine, Durham, NC, USA.
Am J Transplant. 2018 Jul;18(7):1804-1809. doi: 10.1111/ajt.14910. Epub 2018 Jun 9.
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.
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。