Legrand Nicolas, Weijer Kees, Spits Hergen
Department of Cell Biology and Histology, Academic Medical Center of the University of Amsterdam, The Netherlands.
J Immunol. 2006 Feb 15;176(4):2053-8. doi: 10.4049/jimmunol.176.4.2053.
The study of development and function of the immune system in vivo has made intensive use of animal models, but performing such work in humans is difficult for experimental, practical, and ethical reasons. Confronted with this scientific challenge, several pioneering groups have developed in the late 1980s mouse models of human immune system development. Although these experimental approaches were proven successful and useful, they were suffering from limitations due to xenograft transplantation barriers. By reviewing the characteristics of the successive models over the last 20 years, it becomes apparent that screening of potentially interesting mouse strains and usage of combinations of genetic deficiencies has led to major advances. This is particularly true for human T cell development in the murine thymus. This review will focus on these advances and the potential future improvements that remain to be accomplished.
体内免疫系统发育和功能的研究大量使用了动物模型,但由于实验、实际操作及伦理等原因,在人体中开展此类研究存在困难。面对这一科学挑战,几个先驱团队在20世纪80年代末开发了人类免疫系统发育的小鼠模型。尽管这些实验方法已被证明是成功且有用的,但由于异种移植障碍,它们存在局限性。通过回顾过去20年中相继出现的模型的特点,很明显对潜在有趣的小鼠品系进行筛选以及使用基因缺陷组合已带来了重大进展。在小鼠胸腺中人类T细胞发育方面尤其如此。本综述将聚焦于这些进展以及有待实现的潜在未来改进。