Maymon Eli, Romero Roberto, Bhatti Gaurav, Chaemsaithong Piya, Gomez-Lopez Nardhy, Panaitescu Bogdan, Chaiyasit Noppadol, Pacora Percy, Dong Zhong, Hassan Sonia S, Erez Offer
Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, MD, and Detroit, MI, USA.
J Perinat Med. 2018 Feb 23;46(2):123-137. doi: 10.1515/jpm-2017-0042.
The objective of this study is to determine whether the amniotic fluid (AF) concentration of soluble CXCR3 and its ligands CXCL9 and CXCL10 changes in patients whose placentas show evidence of chronic chorioamnionitis or other placental lesions consistent with maternal anti-fetal rejection.
This retrospective case-control study included 425 women with (1) preterm delivery (n=92); (2) term in labor (n=68); and (3) term not in labor (n=265). Amniotic fluid CXCR3, CXCL9 and CXCL10 concentrations were determined by ELISA.
(1) Amniotic fluid concentrations of CXCR3 and its ligands CXCL9 and CXCL10 are higher in patients with preterm labor and maternal anti-fetal rejection lesions than in those without these lesions [CXCR3: preterm labor and delivery with maternal anti-fetal rejection placental lesions (median, 17.24 ng/mL; IQR, 6.79-26.68) vs. preterm labor and delivery without these placental lesions (median 8.79 ng/mL; IQR, 4.98-14.7; P=0.028)]; (2) patients with preterm labor and chronic chorioamnionitis had higher AF concentrations of CXCL9 and CXCL10, but not CXCR3, than those without this lesion [CXCR3: preterm labor with chronic chorioamnionitis (median, 17.02 ng/mL; IQR, 5.57-26.68) vs. preterm labor without chronic chorioamnionitis (median, 10.37 ng/mL; IQR 5.01-17.81; P=0.283)]; (3) patients with preterm labor had a significantly higher AF concentration of CXCR3 than those in labor at term regardless of the presence or absence of placental lesions.
Our findings support a role for maternal anti-fetal rejection in a subset of patients with preterm labor.
本研究旨在确定胎盘显示慢性绒毛膜羊膜炎证据或其他与母体抗胎儿排斥相符的胎盘病变的患者,其羊水(AF)中可溶性CXCR3及其配体CXCL9和CXCL10的浓度是否发生变化。
这项回顾性病例对照研究纳入了425名女性,她们分别为:(1)早产(n = 92);(2)足月临产(n = 68);(3)足月未临产(n = 265)。采用酶联免疫吸附测定法(ELISA)测定羊水CXCR3、CXCL9和CXCL10的浓度。
(1)早产且有母体抗胎儿排斥病变的患者,其羊水CXCR3及其配体CXCL9和CXCL10的浓度高于无这些病变的患者[CXCR3:早产且有母体抗胎儿排斥胎盘病变(中位数,17.24 ng/mL;四分位间距,6.79 - 26.68) vs. 早产且无这些胎盘病变(中位数8.79 ng/mL;四分位间距,4.98 - 14.7;P = 0.028)];(2)早产且有慢性绒毛膜羊膜炎的患者,其羊水CXCL9和CXCL10的浓度高于无此病变的患者,但CXCR3浓度无差异[CXCR3:早产且有慢性绒毛膜羊膜炎(中位数,17.02 ng/mL;四分位间距,5.57 - 26.68) vs. 早产且无慢性绒毛膜羊膜炎(中位数,10.37 ng/mL;四分位间距5.01 - 17.81;P = 0.283)];(3)无论有无胎盘病变,早产患者羊水CXCR3的浓度均显著高于足月临产患者。
我们的研究结果支持母体抗胎儿排斥在一部分早产患者中起作用。