Newborn susceptibility to infection vs. disease depends on complex in vivo interactions of host and pathogen

被引:32
作者
Brook, Byron [1 ]
Harbeson, Danny [1 ]
Ben-Othman, Rym [3 ]
Viemann, Dorothee [2 ]
Kollmann, Tobias R. [1 ,3 ]
机构
[1] Univ British Columbia, Dept Expt Med, BCCHRI A5-175,950 28th Ave, Vancouver, BC V5Z 4H4, Canada
[2] Hannover Med Sch, Dept Pediat Pneumol Allergol & Neonatol, Hannover, Germany
[3] Univ British Columbia, Dept Pediat, Div Infect Dis, Vancouver, BC, Canada
关键词
NEONATAL IMMUNE-SYSTEM; INNATE IMMUNITY; T-CELLS; EMERGENCY MYELOPOIESIS; ADAPTIVE IMMUNITY; S100; PROTEINS; RESPONSES; SEPSIS; TOLERANCE; BLOOD;
D O I
10.1007/s00281-017-0651-z
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 burden of newborn infectious disease has long been recognized as the highest across the entire human life span. The precise underlying cause is unfortunately still far from clear. A substantial body of data derived mostly from in vitro experimentation indicates "lower" host immune responses in early vs. adult life and is briefly summarized within this review. However, emerging data derived mostly from in vivo experimentation reveal that the newborn host also exhibits an exuberant immune and inflammatory response following infection when compared to the adult. In this context, it is important to emphasize that "infection" does not equate "infectious disease," as for many infections it is the host response to the infection that causes disease. This simple insight readily arranges existing evidence into cause-effect relationships that explain much of the increase in clinical suffering from infection in early life. We here briefly summarize the evidence in support of this paradigm and highlight the important implications it has for efforts to ameliorate the suffering and dying from infection in early life.
引用
收藏
页码:615 / 625
页数:11
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