Mouse and human intestinal immunity: same ballpark, different players; different rules, same score

被引:115
作者
Gibbons, D. L. [1 ,2 ]
Spencer, J. [1 ]
机构
[1] Kings Coll London, Peter Gorer Dept Immunobiol, London WC2R 2LS, England
[2] Guys & St Thomas NHS Trust, Biomed Res Ctr, NIHR, London, England
关键词
ARYL-HYDROCARBON RECEPTOR; REGULATORY T-CELLS; SEGMENTED FILAMENTOUS BACTERIA; FOLLICLE-ASSOCIATED EPITHELIUM; ISOLATED LYMPHOID FOLLICLES; CLASS SWITCH RECOMBINATION; TISSUE-INDUCER CELLS; HUMAN PEYERS-PATCHES; GROWTH-FACTOR-BETA; TGF-BETA;
D O I
10.1038/mi.2010.85
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The study of animal immune physiology and animal models of human disease have accelerated many aspects of translational research by allowing direct, definitive investigations. In particular, the use of mice has allowed genetic manipulation, adoptive transfer, immunization, and focused cell and tissue sampling, which would obviously be unthinkable for studies in humans. However, the disease relevance of some animal models may be uncertain and difficulties in interpretation may occur as a consequence of immunological differences between the two species. In this review, we will consider general differences in the structure and development of human and mouse mucosal lymphoid microenvironments and then discuss species differences in mucosal B- and T-cell biology that relate to the current concepts of intestinal immune function.
引用
收藏
页码:148 / 157
页数:10
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