Sundberg John P, King Lloyd E
The Jackson Laboratory, Bar Harbor, Maine 04609-1500, USA.
J Investig Dermatol Symp Proc. 2003 Oct;8(2):173-5. doi: 10.1046/j.1087-0024.2003.00804.x.
Laboratory mice have become the premier animal model for most human and domestic animal diseases, and they have long been the model of choice for studying mammalian genetics, especially since the advent of genetic engineering. Many remarkable discoveries have been made through intense study of these wonderful small mammals, and undoubtably many more will be made. It is no surprise that one mouse model for alopecia areata (AA) has been found possibly many more will be, some of which exhibit rare phenotypes found in subpopulations of humans with the disease, such as nail deformities, thyroid disease, inflammatory bowel disease, and autoimmune polyendocrine syndrome type 1. Intense investigation by many groups into the first model, the adult onset form of AA (using the C3H/HeJ inbred strain), found similarities as well as differences with commonly held ideas concerning human AA. Regardless of some of the controversies, much insight has been gained from studying these and other rodent and domestic animal models which has opened up new ideas and discussions of AA and its treatment.
实验小鼠已成为大多数人类和家畜疾病的首要动物模型,长期以来一直是研究哺乳动物遗传学的首选模型,尤其是自基因工程出现以来。通过对这些奇妙的小型哺乳动物的深入研究,已经取得了许多显著的发现,毫无疑问,未来还会有更多发现。毫不奇怪,已经发现了一种斑秃(AA)小鼠模型,可能还会有更多,其中一些表现出在患有该疾病的人类亚群中发现的罕见表型,如指甲畸形、甲状腺疾病、炎症性肠病和1型自身免疫性多内分泌综合征。许多研究小组对第一个模型,即成年发病型AA(使用C3H/HeJ近交系)进行了深入研究,发现了与关于人类AA的普遍观点的异同。尽管存在一些争议,但通过研究这些以及其他啮齿动物和家畜模型,已经获得了很多见解,这为AA及其治疗开辟了新的思路和讨论。