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猪到非人灵长类动物器官移植中免疫抑制疗法的演变

The Evolution of Immunosuppressive Therapy in Pig-to-Nonhuman Primate Organ Transplantation.

作者信息

Sanatkar S A, Kinoshita K, Maenaka A, Hara H, Cooper D K C

机构信息

Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.

The Transplantation Institute at the Second Affiliated Hospital of Hainan Medical University, Haikou, Hainan, China.

出版信息

Transpl Int. 2025 Jan 13;37:13942. doi: 10.3389/ti.2024.13942. eCollection 2024.

Abstract

An overview is provided of the evolution of strategies towards xenotransplantation during the past almost 40 years, focusing on advances in gene-editing of the organ-source pigs, pre-transplant treatment of the recipient, immunosuppressive protocols, and adjunctive therapy. Despite initial challenges, including hyperacute rejection resulting from natural (preformed) antibody binding and complement activation, significant progress has been made through gene editing of the organ-source pigs and refinement of immunosuppressive regimens. Major steps were the identification and deletion of expression of the three known glycan xenoantigens on pig vascular endothelial cells, the transgenic expression of human "protective" proteins, e.g., complement-regulatory, coagulation-regulatory, and anti-inflammatory proteins, and the administration of an immunosuppressive regimen based on blockade of the CD40/CD154 T cell co-stimulation pathway. Efforts to address systemic inflammation followed. The synergy between gene editing and judicious immunomodulation appears to largely prevent graft rejection and is associated with a relatively good safety profile. Though there remains an incidence of severe or persistent proteinuria (nephrotic syndrome) in a minority of cases. This progress offers renewed hope for patients in need of life-saving organ transplants.

摘要

本文概述了近40年来异种移植策略的演变,重点关注器官源猪的基因编辑、受体的移植前治疗、免疫抑制方案和辅助治疗方面的进展。尽管最初面临挑战,包括天然(预先形成的)抗体结合和补体激活导致的超急性排斥反应,但通过对器官源猪的基因编辑和免疫抑制方案的优化,已经取得了显著进展。主要步骤包括识别和删除猪血管内皮细胞上三种已知聚糖异种抗原的表达、人类“保护”蛋白(如补体调节、凝血调节和抗炎蛋白)的转基因表达,以及基于阻断CD40/CD154 T细胞共刺激途径的免疫抑制方案的应用。随后人们努力解决全身炎症问题。基因编辑与明智的免疫调节之间的协同作用似乎在很大程度上防止了移植物排斥反应,并且具有相对良好的安全性。尽管在少数情况下仍有严重或持续性蛋白尿(肾病综合征)的发生率。这一进展为需要挽救生命的器官移植的患者带来了新的希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c27/11770881/94792b7e2a0b/ti-37-13942-g001.jpg

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