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DOI 10.1111/j.1600-0897.2006.00394.x

Медицинская библиотека · American journal of reproductive immunology (New York, N.Y. : 1989) · 2006

Differences in the placental membrane cytokine response: a possible explanation for the racial disparity in preterm birth.

Menon Ramkumar, Merialdi Mario, Lombardi Salvatore J, Fortunato Stephen J

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

PROBLEM: The prematurity rate is higher in African-Americans (AA) compared with Caucasians (C). As spontaneous preterm labor has been hypothesized to be a host inflammatory response disease racial differences in human placental membrane inflammatory cytokine and prostaglandin pathway gene expression patterns between AA and C were examined in this report.

METHOD OF STUDY: Placental membranes (amniochorion) collected from AA and C women from cesareans at term were maintained in an organ explant system and stimulated with endotoxin (lipopolysaccharide, LPS). Microarray analysis and enzyme-linked immunosorbent assay was performed on mRNAs and culture media from AA- and C-derived membranes to document any differences in mRNA expression and protein production of IL-1, IL-6, IL-8, IL-10 and expression of cyclooxygenase 1 (COX-1), COX-2 and 15-hydroxyprostaglandin dehydrogenase (PGDH).

RESULTS

Increased mRNA expression of IL-1, IL-8 and COX-2 in AA and IL-6, IL-10, COX-1 and PGDH in C were documented after LPS stimulation. Concentration of IL-1 was significantly higher in media derived from AA whereas IL-6 and IL-10 concentrations were higher in C with no differences observed in IL-8 after LPS stimulation compared with respective unstimulated controls.

CONCLUSION

These data document ethnic diversity in placental membrane immune response.

Для цитирования: Menon Ramkumar, Merialdi Mario, Lombardi Salvatore J, Fortunato Stephen J. Differences in the placental membrane cytokine response: a possible explanation for the racial disparity in preterm birth.. American journal of reproductive immunology (New York, N.Y. : 1989). 2006. DOI: 10.1111/j.1600-0897.2006.00394.x.

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