TY - JOUR
T1 - Fragment Bb
T2 - Evidence for activation of the alternative pathway of the complement system in pregnant women with acute pyelonephritis
AU - Soto, Eleazar
AU - Romero, Roberto
AU - Vaisbuch, Edi
AU - Erez, Offer
AU - Mazaki-Tovi, Shali
AU - Kusanovic, Juan Pedro
AU - Dong, Zhong
AU - Chaiworapongsa, Tinnakorn
AU - Yeo, Lami
AU - Mittal, Pooja
AU - Hassan, Sonia S.
N1 - Funding Information:
This research was supported by the Perinatology Research Branch, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, DHHS.
PY - 2010/10/1
Y1 - 2010/10/1
N2 - Objective.Pyelonephritis during pregnancy is associated with a more severe course than in the non-pregnant state. This has been attributed to an increased susceptibility of pregnant women to microbial products. The complement system is part of innate immunity and its alternative pathway is activated mainly by microorganisms. The purpose of this study was to determine if activation of the alternative pathway of the complement system (determined by maternal fragment Bb concentrations) occurs in pregnant women with acute pyelonephritis. Methods.This cross-sectional study included the following groups: (1) normal pregnant women (n62) and (2) pregnant women with pyelonephritis (n38). Maternal plasma fragment Bb concentrations were determined by ELISA. Non-parametric statistics were used for analyses. Results.(1) Pregnant women with pyelonephritis had a higher median plasma concentration of fragment Bb than those with a normal pregnancy (1.3μg/ml, IQR: 1.11.9 vs. 0.8μg/ml, IQR: 0.70.9; p<0.001); (2) No significant differences were observed in the median maternal plasma concentration of fragment Bb between pregnant women with pyelonephritis who had a positive blood culture and those with a negative blood culture (1.4μg/ml, IQR: 1.13.5 vs. 1.3μg/ml, IQR: 1.11.9; p0.2). Conclusions.Pregnant women with acute pyelonephritis have evidence of activation of the alternative pathway of the complement system, regardless of the presence or absence of a positive blood culture.
AB - Objective.Pyelonephritis during pregnancy is associated with a more severe course than in the non-pregnant state. This has been attributed to an increased susceptibility of pregnant women to microbial products. The complement system is part of innate immunity and its alternative pathway is activated mainly by microorganisms. The purpose of this study was to determine if activation of the alternative pathway of the complement system (determined by maternal fragment Bb concentrations) occurs in pregnant women with acute pyelonephritis. Methods.This cross-sectional study included the following groups: (1) normal pregnant women (n62) and (2) pregnant women with pyelonephritis (n38). Maternal plasma fragment Bb concentrations were determined by ELISA. Non-parametric statistics were used for analyses. Results.(1) Pregnant women with pyelonephritis had a higher median plasma concentration of fragment Bb than those with a normal pregnancy (1.3μg/ml, IQR: 1.11.9 vs. 0.8μg/ml, IQR: 0.70.9; p<0.001); (2) No significant differences were observed in the median maternal plasma concentration of fragment Bb between pregnant women with pyelonephritis who had a positive blood culture and those with a negative blood culture (1.4μg/ml, IQR: 1.13.5 vs. 1.3μg/ml, IQR: 1.11.9; p0.2). Conclusions.Pregnant women with acute pyelonephritis have evidence of activation of the alternative pathway of the complement system, regardless of the presence or absence of a positive blood culture.
KW - Acute respiratory distress syndrome
KW - Th1/Th2
KW - asymptomatic bacteriuria
KW - inflammation
KW - innate immunity
KW - pregnancy
KW - urinary tract infection
UR - http://www.scopus.com/inward/record.url?scp=77956609423&partnerID=8YFLogxK
U2 - 10.3109/14767051003649870
DO - 10.3109/14767051003649870
M3 - Article
AN - SCOPUS:77956609423
SN - 1476-7058
VL - 23
SP - 1085
EP - 1090
JO - Journal of Maternal-Fetal and Neonatal Medicine
JF - Journal of Maternal-Fetal and Neonatal Medicine
IS - 10
ER -