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用于研究非协调性异种移植的人CD46转基因猪模型系统。

A human CD46 transgenic pig model system for the study of discordant xenotransplantation.

作者信息

Diamond L E, Quinn C M, Martin M J, Lawson J, Platt J L, Logan J S

机构信息

Nextran, Inc, Princeton, New Jersey 08540, USA.

出版信息

Transplantation. 2001 Jan 15;71(1):132-42. doi: 10.1097/00007890-200101150-00021.

Abstract

BACKGROUND

The chronic shortage in the supply of human organs available for allotransplantation has turned attention toward the use of animals as potential donors, with pigs as the most likely species under consideration. Hyperacute rejection, the initial and immediate barrier to a pig-to-primate xenograft, has been addressed by generation of transgenic pigs that express the human membrane-bound complement-regulatory proteins CD59 and/or CD55. Difficulty has been encountered in generation of transgenic animals that express a third membrane-bound complement-regulatory protein, CD46.

METHODS

We have generated transgenic animals by using a large genomic construct that encompasses the entire human CD46 gene.

RESULTS

We report the first description of transgenic mice and pigs that express high levels of human CD46 in a cell and tissue type-specific manner, resembling patterns of endogenous CD46 expression observed in human tissues. Furthermore, when human CD46 transgenic porcine hearts were transplanted into baboons, the grafts did not succumb to hyperacute rejection, and survival extended for up to 23 days. Under the same conditions, nontransgenic grafts underwent hyperacute rejection within 90 min.

CONCLUSIONS

This is the first report to describe generation of transgenic pigs that express human CD46, and the first in vivo demonstration of the ability of human CD46 expressed on pig organs to regulate complement activation and overcome hyperacute rejection upon transplantation of a vascularized organ into nonhuman primates.

摘要

背景

同种异体移植可用人体器官的长期短缺已将人们的注意力转向将动物作为潜在供体,猪是最有可能被考虑的物种。超急性排斥反应是猪到灵长类动物异种移植的初始和直接障碍,通过培育表达人膜结合补体调节蛋白CD59和/或CD55的转基因猪已得到解决。在培育表达第三种膜结合补体调节蛋白CD46的转基因动物时遇到了困难。

方法

我们通过使用包含整个人类CD46基因的大型基因组构建体培育出了转基因动物。

结果

我们首次描述了以细胞和组织类型特异性方式高水平表达人CD46的转基因小鼠和猪,其表达模式类似于在人体组织中观察到的内源性CD46表达模式。此外,当将人CD46转基因猪心脏移植到狒狒体内时,移植物并未死于超急性排斥反应,存活时间延长至23天。在相同条件下,非转基因移植物在90分钟内发生超急性排斥反应。

结论

这是第一份描述表达人CD46的转基因猪培育情况的报告,也是首次在体内证明猪器官上表达的人CD46在将血管化器官移植到非人灵长类动物体内时调节补体激活并克服超急性排斥反应的能力。

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