Immune responses in neonates

被引:376
作者
Basha, Saleem [1 ]
Surendran, Naveen [1 ]
Pichichero, Michael [1 ]
机构
[1] Rochester Gen Hosp, Res Inst, Ctr Infect Dis & Immunol, Rochester, NY 14621 USA
基金
美国国家卫生研究院;
关键词
adaptive immunity; B cell; BCR; B-reg cell; CD103 dendritic cell; CD5; cell; CD71 erythroid cell; chemokines; cord blood; dendritic cell; IL-27; macrophages; innate immunity; neonates; neutrophils; NK-cell; RTE; T follicular cell; T cell; TCR; Th; 17; toll-like receptor; Treg cell; gamma delta-T cell; REGULATORY T-CELLS; RECENT THYMIC EMIGRANTS; HUMAN CORD BLOOD; B-CELL; INNATE IMMUNITY; ERYTHROID-CELLS; DENDRITIC CELLS; HUMAN NEWBORNS; LOW EXPRESSION; TH1; RESPONSES;
D O I
10.1586/1744666X.2014.942288
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
Neonates have little immunological memory and a developing immune system, which increases their vulnerability to infectious agents. Recent advances in the understanding of neonatal immunity indicate that both innate and adaptive responses are dependent on precursor frequency of lymphocytes, antigenic dose and mode of exposure. Studies in neonatal mouse models and human umbilical cord blood cells demonstrate the capability of neonatal immune cells to produce immune responses similar to adults in some aspects but not others. This review focuses mainly on the developmental and functional mechanisms of the human neonatal immune system. In particular, the mechanism of innate and adaptive immunity and the role of neutrophils, antigen presenting cells, differences in subclasses of T lymphocytes (Th1, Th2, Tregs) and B cells are discussed. In addition, we have included the recent developments in the neonatal mouse immune system. Understanding neonatal immunity is essential to development of therapeutic vaccines to combat newly emerging infectious agents.
引用
收藏
页码:1171 / 1184
页数:14
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