[基因治疗的动物模型]。

Journal de genetique humaine Pub Date : 1989-12-01
P Briand
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引用次数: 0

摘要

体细胞基因疗法是基于在体细胞中引入基因,试图纠正基因缺陷,诱导抗性或增加特定活性。在原理上,它们与器官移植没有太大的区别,也不存在特定的伦理问题。它们在人类治疗中的应用必须经过对其无害性和有效性的严格评估。为此,体细胞基因治疗的动物模型是必不可少的。这种疗法已经在骨髓和内皮细胞、成纤维细胞、角化细胞、肝细胞中进行了试验,但也通过直接在生物体中转移基因进行了试验。本文对这些不同的方法进行了简要的回顾和比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Animal models of gene therapy].

Somatic gene therapies are based on the introduction of genes in somatic cells in an attempt to correct a gene defect, to induce a resistance or to add a particular activity. In their principle, they are not very different from organ grafts and do not set specific ethic problems. Their application to human therapy has to be subjected to a critical evaluation of their harmlessness and efficiency. For this purpose, animal models of somatic gene therapy are essential. Such therapy have been tried in bone marrow and endothelial cells, in fibroblasts, keratinocytes hepatocytes, but also by direct transfer of genes in the organism. These different approaches are briefly reviewed and compared in this article.

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