Pigs in Transplantation Research and Their Potential as Sources of Organs in Clinical Xenotransplantation.

Comparative medicine Pub Date : 2024-04-01 Epub Date: 2024-02-15 DOI:10.30802/AALAS-CM-23-000030
S Sikandar Raza, Hidetaka Hara, Willard Eyestone, David Ayares, David C Cleveland, David K C Cooper
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Abstract

The pig has long been used as a research animal and has now gained importance as a potential source of organs for clinical xenotransplantation. When an organ from a wild-type (i. e., genetically unmodified) pig is transplanted into an immunosuppressed nonhuman primate, a vigorous host immune response causes hyperacute rejection (within minutes or hours). This response has been largely overcome by 1) extensive gene editing of the organ-source pig and 2) the administration to the recipient of novel immunosuppressive therapy based on blockade of the CD40/CD154 T cell costimulation pathway. Gene editing has consisted of 1) deletion of expression of the 3 known carbohydrate xenoantigens against which humans have natural (preformed) antibodies and 2) the introduction of human 'protective' genes. The combination of gene editing and novel immunosuppressive therapy has extended life-supporting pig kidney graft survival to greater than 1 y and of pig heart survival to up to 9 mo. This review briefly describes the techniques of gene editing, the potential risks of transfer of porcine endogenous retroviruses with the organ, and the need for breeding and housing of donor pigs under biosecure conditions.

移植研究中的猪及其作为临床异种移植器官来源的潜力。
长期以来,猪一直被用作研究动物,现在作为临床异种移植的潜在器官来源,其重要性日益凸显。当来自野生型猪(即基因未修改的猪)的器官移植到免疫抑制的非人灵长类动物体内时,强烈的宿主免疫反应会导致超急性排斥反应(数分钟或数小时内)。这种反应在很大程度上是通过以下方法克服的:1)对器官来源猪进行广泛的基因编辑;2)向受体施用基于阻断 CD40/CD154 T 细胞成本刺激途径的新型免疫抑制疗法。基因编辑包括:1)删除人类具有天然(预形成)抗体的 3 种已知碳水化合物异抗原的表达;2)引入人类 "保护 "基因。基因编辑与新型免疫抑制疗法相结合,已将维持生命的猪肾脏移植存活期延长至 1 年以上,猪心脏存活期延长至 9 个月。 本综述简要介绍了基因编辑技术、猪内源性逆转录病毒随器官转移的潜在风险,以及在生物安全条件下繁殖和饲养供体猪的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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