异种移植:最先进的技术。

Forum (Genoa, Italy) Pub Date : 1999-07-01
M Lavitrano, L Frati
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引用次数: 0

摘要

不幸的是,器官移植受到可用的人体尸体供体器官数量的限制。异种移植——在动物物种之间进行器官和组织的移植——将提供无限数量的器官,并带来许多其他优势。作为异种移植器官来源的主要候选者是猪,因为它在解剖学和生理学上与人类相似。然而,远亲物种之间的器官移植会导致移植的超急性排斥反应(HAR),这是一种涉及补体系统的强烈免疫反应,当器官在远亲之间移植时,如猪和人,就会释放出来。HAR破坏移植器官中的血管,并在几分钟内杀死它们。补体攻击是由于抗体介导的补体级联激活(人类抗猪抗体已被鉴定为直接针对猪血管内皮上的gal -a1-3半乳糖表位),这种现象在生理上受到一组物种特异性蛋白的负调控,这些蛋白被称为补体激活调节剂(RCA),如衰变加速因子(DAF)、膜辅因子蛋白(MCP)和CD59。如果哺乳动物细胞在体外表达人RCA,细胞可以防止人补体的裂解。因此,通过转基因将人RCA结合到异种器官中可以保护移植的器官或组织免受体内人补体的溶解。人们正在努力克服这种超急性排斥反应。正在研究的方法包括:1 .消耗或抑制受体抗体或补体;2受体对猪器官免疫耐受的发展ⅲ。开发不表达a- gal表位和/或表达人类补体抑制蛋白(即DAF)的转基因猪。包括我们小组在内的少数研究小组已经开始了为人类RCA之一生产转基因猪的计划,试图生产出器官适合移植到人类身上的动物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Xenotransplantation: state of the art.

Organ transplantation is unfortunately limited by the number of cadaveric human donor organs that become available. Xenotransplantation - the transplantation of organs and tissues between animal species - would supply an unlimited number of organs and offer many other advantages. The leading candidate as a source of organs for xenotransplantation is the pig, as it is anatomically and physiologically similar to man. However, organ transplantation between distantly related species results in hyperacute rejection (HAR) of the transplant, which consists of a violent immune response involving the complement system, unleashed when organs are transplanted between distant relatives, such as pigs and humans. HAR destroys the blood vessels in the transplanted organs and kills them within minutes. Complement attack is due to the antibody-mediated activation of the complement cascade (human anti-pig antibodies have been identified as being directed against Gal-a1-3galactose epitopes on pig vascular endothelium), and this phenomenon is physiologically subjected to negative regulation by a set of species-specific proteins, known as regulators of complement activation (RCA), such as decay accelerating factor (DAF), membrane cofactor protein (MCP) and CD59. If human RCA are expressed by mammalian cells in vitro, the cells are protected against the lysis by human complement. Therefore the incorporation of human RCA into a xenogeneic organ by transgenesis should protect the transplanted organ or tissue from in vivo lysis by human complement. Major efforts are being made to overcome this hyperacute rejection. Methods being investigated include: i. depletion or inhibition of recipient antibodies or complement; ii. development of immunological tolerance to pig organs in the recipient; and iii. development of transgenic pigs that do not express the a-Gal epitope and/or express a human complement inhibiting protein (i.e., DAF). A small number of research teams, including our group, have embarked on programs to produce transgenic pigs for one of the human RCA, in the attempt to produce animals whose organs may be suitable for transplantation into humans.

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