Genetic models of human and mouse dendritic cell development and function

被引:0
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作者
David A. Anderson
Charles-Antoine Dutertre
Florent Ginhoux
Kenneth M. Murphy
机构
[1] Washington University in St. Louis,Department of Pathology and Immunology, School of Medicine
[2] Singapore Immunology Network,Shanghai Institute of Immunology, Department of Immunology and Microbiology
[3] Agency for Science,Howard Hughes Medical Institute, School of Medicine
[4] Technology and Research,undefined
[5] Shanghai Jiao Tong University School of Medicine,undefined
[6] Translational Immunology Institute,undefined
[7] SingHealth Duke-NUS Academic Medical Centre,undefined
[8] Washington University in St. Louis,undefined
来源
Nature Reviews Immunology | 2021年 / 21卷
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摘要
Dendritic cells (DCs) develop in the bone marrow from haematopoietic progenitors that have numerous shared characteristics between mice and humans. Human counterparts of mouse DC progenitors have been identified by their shared transcriptional signatures and developmental potential. New findings continue to revise models of DC ontogeny but it is well accepted that DCs can be divided into two main functional groups. Classical DCs include type 1 and type 2 subsets, which can detect different pathogens, produce specific cytokines and present antigens to polarize mainly naive CD8+ or CD4+ T cells, respectively. By contrast, the function of plasmacytoid DCs is largely innate and restricted to the detection of viral infections and the production of type I interferon. Here, we discuss genetic models of mouse DC development and function that have aided in correlating ontogeny with function, as well as how these findings can be translated to human DCs and their progenitors.
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页码:101 / 115
页数:14
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