Journal
PEDIATRIC RESEARCH
Volume 73, Issue 5, Pages 685-691Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/pr.2013.36
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Funding
- National Science Council of Taiwan [NSC 98-2320-B-010-016-MY3]
- Institute of Medical Research of the Cathay General Hospital [MR9514]
- Ministry of Education, Aim for the Top University Plan, Taiwan
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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.
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