Advanced model systems and tools for basic and translational human immunology

被引:73
|
作者
Wagar, Lisa E. [1 ]
DiFazio, Robert M. [2 ]
Davis, Mark M. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Inst Immun Transplantat & Infect, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
来源
GENOME MEDICINE | 2018年 / 10卷
基金
美国国家卫生研究院;
关键词
NONHUMAN PRIMATE MODELS; HUMAN IMMUNE-SYSTEM; NEUTRALIZING ANTIBODY-RESPONSES; TUMOR-INFILTRATING LYMPHOCYTES; CELL-RECEPTOR SEQUENCES; BLOOD MONONUCLEAR-CELLS; NAIVE T-CELLS; ON-A-CHIP; IMMUNODEFICIENT MICE; PERIPHERAL-BLOOD;
D O I
10.1186/s13073-018-0584-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There are fundamental differences between humans and the animals we typically use to study the immune system. We have learned much from genetically manipulated and inbred animal models, but instances in which these findings have been successfully translated to human immunity have been rare. Embracing the genetic and environmental diversity of humans can tell us about the fundamental biology of immune cell types and the elasticity of the immune system. Although people are much more immunologically diverse than conventionally housed animal models, tools and technologies are now available that permit high-throughput analysis of human samples, including both blood and tissues, which will give us deep insights into human immunity in health and disease. As we gain a more detailed picture of the human immune system, we can build more sophisticated models to better reflect this complexity, both enabling the discovery of new immunological mechanisms and facilitating translation into the clinic.
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页数:14
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