Repeated Lipopolysaccharide Exposure Leads To Placental Endotoxin Tolerance

Maureen L Kim, Caroline Maloney,Natalia Klimova,Ellen Gurzenda,Xinhua Lin,Yuko Arita, Treasure Walker,Melissa J Fazzari,Nazeeh Hanna

AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY(2019)

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摘要
Problem Placental infection induces increased levels of pro-inflammatory cytokines, which have been implicated in the pathogenesis of pre-term labor. Endotoxin tolerance is a phenomenon in which exposure to a dose of endotoxin makes tissue less responsive to subsequent exposures. The objective of our study was to determine whether repeated exposure to endotoxin will induce a tolerant phenotype in normal human second-trimester placental tissue. Methods of study Human second-trimester placental explants from elective termination of pregnancy were cultured and exposed to endotoxin (LPS). After 24 hours, the media was collected for analysis, and the explants were re-exposed to LPS after adding fresh media for another 24 hours. This process was repeated for a total of 4 LPS doses. The media was collected from each day and analyzed for cytokine levels. Results The first LPS treatment stimulated the secretion of the pro-inflammatory cytokines IL-1 beta and TNF-alpha. However, their production was significantly diminished with repeated LPS doses. Production of the anti-inflammatory cytokines, IL-1ra and IL-10, was also stimulated by the first LPS treatment, but secretion was more gradually and moderately decreased with repeated LPS doses compared to the pro-inflammatory cytokines. The ratios of the anti-inflammatory/pro-inflammatory mediators (IL-1ra/IL-1 beta and IL-10/TNF-alpha) indicate a progressively more anti-inflammatory milieu with repeated LPS doses. Conclusion Repeated LPS exposure of human second-trimester placental tissues induced endotoxin tolerance. We speculate that endotoxin tolerance at the maternal-fetal interface will protect the fetus from exaggerated inflammatory responses after repeated infectious exposure.
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关键词
endotoxin tolerance, inflammation, LPS, placenta, pre-term labor
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