Rebooting Human Immunology

被引:62
作者
Davis, Mark M. [1 ,2 ]
Brodin, Petter [3 ,4 ]
机构
[1] Stanford Univ, Sch Med, Howard Hughes Med Inst, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Inst Immun Transplantat & Infect, Stanford, CA 94305 USA
[3] Karolinska Inst, Dept Womens & Childrens Hlth, Sci Life Lab, S-17121 Solna, Sweden
[4] Karolinska Univ Hosp, Dept Neonatol, S-17176 Solna, Sweden
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 36 | 2018年 / 36卷
关键词
human immunology; systems immunology; CMV; human evolution; T-CELL-RECEPTOR; HUMAN IMMUNE-SYSTEM; MAMMARY-TUMOR VIRUS; INFLUENZA VACCINATION; SEASONAL INFLUENZA; MOUSE MODEL; RESPONSES; CD4(+); MICE; SIGNATURES;
D O I
10.1146/annurev-immunol-042617-053206
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Recent progress in both conceptual and technological approaches to human immunology have rejuvenated a field that has long been in the shadow of the inbred mouse model. This is a healthy development both for the clinical relevance of immunology and for the fact that it is a way to gain access to the wealth of phenomenology in the many human diseases that involve the immune system. This is where we are likely to discover new immunological mechanisms and principals, especially those involving genetic heterogeneity or environmental influences that are difficult to model effectively in inbred mice. We also suggest that there are likely to be novel immunological mechanisms in long-lived, less fecund mammals such as human beings since they must remain healthy far longer than short-lived rodents in order for the species to survive.
引用
收藏
页码:843 / 864
页数:22
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