Development of monocyte Toll-like receptor 2 and Toll-like receptor 4 in preterm newborns during the first few months of life

被引:21
|
作者
Shen, Chung-Min [1 ,2 ]
Lin, Shih-Chang [3 ]
Niu, Dau-Ming [1 ,4 ]
Kou, Yu Ru [5 ]
机构
[1] Natl Yang Ming Univ, Coll Med, Inst Clin Med, Taipei 112, Taiwan
[2] Cathay Gen Hosp, Dept Pediat, Taipei, Taiwan
[3] Cathay Gen Hosp, Dept Internal Med, Div Allergy & Immunol, Taipei, Taiwan
[4] Vet Gen Hosp, Dept Pediat, Taipei, Taiwan
[5] Natl Yang Ming Univ, Coll Med, Inst Physiol, Taipei 112, Taiwan
关键词
INDUCED CYTOKINE PRODUCTION; NECROSIS-FACTOR-ALPHA; INNATE IMMUNITY; CORD BLOOD; DOWN-REGULATION; EXPRESSION; RESPONSES; LIPOPOLYSACCHARIDE;
D O I
10.1038/pr.2013.36
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: Although the immaturity of Toll-like receptor 2 (TLR2) and Toll-like receptor 4 (TLR4) at birth in preterm newborns is known, their development during the first few months of life remains unclear. METHODS: Blood monocytes of preterm newborns (gestational age: 24-36 wk) were obtained every 2 wk when possible in order to perform serial measurements of TLR2 and TLR4 surface expression, as well as lipopolysaccharide (LPS)-induced cytokine production. Measurements using monocytes from term newborns and adults were also performed. RESULTS: The monocytes of preterm newborns obtained at birth displayed reduced surface expression of TLR2 and TLR4, and diminished responses of tumor necrosis factor-alpha (INF-alpha) and interleukin (IL)-8 to [PS stimulation. Regardless of gestational age, monocyte expression of TLR2 and TLR4 in preterm newborns increased rapidly within the first 2 wk after birth, quickly reaching those of term newborns. These increases continued for the following 4-6 wk, although the increase began to plateau. By contrast, [PS-induced production of INF-a and IL-8 did not elevate over this period in preterm newborns. CONCLUSION: The blood monocytes of preterm newborns display rapid increase in TLR2 and TLR4 expression during the first few months of life, whereas LPS-induced cytokine production functionality did not improve in parallel.
引用
收藏
页码:685 / 691
页数:7
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