Skewed pattern of Toll-like receptor 4-mediated cytokine production in human neonatal blood: Low LPS-induced IL-12p70 and high IL-10 persist throughout the first month of life

被引:115
作者
Belderbos, M. E. [1 ]
van Bleek, G. M. [1 ]
Levy, O. [2 ,3 ]
Blanken, M. O. [1 ]
Houben, M. L. [1 ]
Schuijff, L. [1 ]
Kimpen, J. L. L. [1 ]
Bont, L. [1 ]
机构
[1] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, NL-3508 AB Utrecht, Netherlands
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Childrens Hosp, Boston, MA 02115 USA
关键词
Neonate; Newborn; Innate immunity; Toll-like receptor; Infection; RESPIRATORY SYNCYTIAL VIRUS; INNATE IMMUNITY; INTERFERON-GAMMA; HUMAN NEWBORN; BACTERIAL-INFECTIONS; ADAPTIVE IMMUNITY; DENDRITIC CELLS; CORD BLOOD; INTERLEUKIN-12; RESPONSES;
D O I
10.1016/j.clim.2009.07.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Newborns are highly susceptible to infectious diseases, which may be due to impaired immune responses. This study aims to characterize the ontogeny of neonatal TLR-based innate immunity during the first month of life. Cellularity and Toll-like receptor (TLR) agonist-induced cytokine production were compared between cord blood obtained from healthy neonates born after uncomplicated gestation and delivery (n = 18), neonatal venous blood obtained at the age of one month (n = 96), and adult venous blood (n=17). Cord blood TLR agonist-induced production of the Th1-polarizing cytokines IL-12p70 and IFN-alpha was generally impaired, but for TLR3, 7 and 9 agonists, rapidly increased to adult levels during the first month of life. In contrast, TLR4 demonstrated a slower maturation, with low LPS-induced IL-12p70 production and high IL-10 production up until the age of one month. Polarization in neonatal cytokine responses to LIPS could contribute to neonatal susceptibility to severe bacterial infection. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:228 / 237
页数:10
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