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大型动物模型与基因治疗。

Large animal models and gene therapy.

作者信息

Casal Margret, Haskins Mark

机构信息

School of Veterinary Medicine, University of Pennsylvania, Philadelphia, 19104-6051, USA.

出版信息

Eur J Hum Genet. 2006 Mar;14(3):266-72. doi: 10.1038/sj.ejhg.5201535.

Abstract

Over the last two decades, gene transfer experiments for the treatment of inherited or acquired diseases have mainly been performed in mice. While mice provide proof of principle and allow testing of a variety of therapeutic modalities, mouse models have some limitations, as only short-term experiments can be performed, their homogenous genetic background is unlike humans, and the knockout models do not always faithfully represent the human disease. Naturally occurring large animal models of human genetic diseases have become increasingly important despite the costs and the extensive clinical attention they require because of their similarities to human patients. Large animals are reasonably outbred, long lived allowing for longitudinal studies, are more similar in size to a neonate or small child providing an opportunity to address issues related to scaling up therapy, and many physiological parameters including the immune system are more similar to those in humans versus those in mice.

摘要

在过去二十年中,用于治疗遗传性或后天性疾病的基因转移实验主要在小鼠身上进行。虽然小鼠提供了原理证明,并允许测试各种治疗方式,但小鼠模型存在一些局限性,因为只能进行短期实验,它们同质的遗传背景与人类不同,而且基因敲除模型并不总是能如实反映人类疾病。尽管人类遗传疾病的天然大型动物模型成本高昂且需要大量临床关注,但由于它们与人类患者相似,已变得越来越重要。大型动物具有适度的远交性、寿命长,适合进行纵向研究,体型与新生儿或幼儿更相似,为解决扩大治疗规模相关问题提供了机会,而且包括免疫系统在内的许多生理参数与人类的比与小鼠的更相似。

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