Diversity in cytokine response to bacteria associated with preterm birth by fetal membranes

被引:68
|
作者
Menon, Ramkumar [1 ,2 ,6 ]
Peltier, Morgan R. [3 ,4 ]
Eckardt, Judith [6 ]
Fortunato, Stephen J. [5 ,6 ]
机构
[1] Emory Univ, Rollins Sch Publ Hlth, Dept Epidemiol, Atlanta, GA 30322 USA
[2] Yale Univ, Sch Med, Dept Obstet & Gynecol & Reprod Med, New Haven, CT USA
[3] Winthrop Univ Hosp, Dept Obstet & Gynecol, Mineola, NY 11501 USA
[4] Winthrop Univ Hosp, Dept Pediat, Mineola, NY 11501 USA
[5] Maternal Fetal Grp PediatriX, Nashville, TN USA
[6] Centennial Womens Hosp, Perinatal Res Ctr, Nashville, TN USA
关键词
amniochorion; inflammation; intraamniotic infection; preterm birth; prostaglandins; AMNIOTIC-FLUID SLUDGE; NECROSIS-FACTOR-ALPHA; GROUP-B STREPTOCOCCI; UREAPLASMA-UREALYTICUM; INTRAUTERINE INFECTION; CLINICAL-SIGNIFICANCE; IN-VITRO; MICROBIAL INVASION; PREMATURE RUPTURE; LABOR;
D O I
10.1016/j.ajog.2009.06.027
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: This study compared cytokine and prostaglandin (PG) responses by fetal membranes stimulated with 4 different bacterial species associated with preterm birth (PTB). STUDY DESIGN: Fetal membranes (n = 13 from normal term cesarean sections [not in labor]) in an organ explant system were stimulated with heat-killed Ureaplasma parvum, Gardanerella vaginalis, Escherichia coli, group 8 Streptococcus (GBS), or lipopolysaccharide (LPS) Cytokines (interleukin [IL]-1 beta, IL-6, IL-8, IL-10, tumor necrosis factor [TNF]-alpha, and interferon-gamma) and PG (PGF(2 alpha) and PGE(2)) concentrations were quantilated and compared RESULTS: LPS and E coli increased all cytokine and PG productions compared with controls. Cytokine profiles were similar after G vaginalis and GBS stimulation. G vaginalis increased PGE(2), whereas GBS increased PGF(2 alpha). U parvum demonstrated the mildest response with only IL-10 and TNF-alpha concentrations being higher with no detectible effect on PGs. CONCLUSION: Fetal membrane cytokine signatures of 4 different bacteria associated with PTB are distinct, suggesting that infection as a potential cause of PTB is not homogeneous in its presentation
引用
收藏
页码:306.e1 / 306.e6
页数:6
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