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腺相关病毒2型(AAV-2)会导致滋养层细胞功能障碍,胎盘AAV-2感染与子痫前期有关。

Adeno-associated virus-2 (AAV-2) causes trophoblast dysfunction, and placental AAV-2 infection is associated with preeclampsia.

作者信息

Arechavaleta-Velasco Fabian, Ma Yujie, Zhang Jian, McGrath Cindy M, Parry Samuel

机构信息

Center for Research on Reproduction and Women's Health, University of Pennsylvania School of Medicine, 421 Curie Blvd., Philadelphia, PA 19104-6160, USA.

出版信息

Am J Pathol. 2006 Jun;168(6):1951-9. doi: 10.2353/ajpath.2006.050781.

Abstract

Shallow invasion by extravillous trophoblast cells into the uterine wall reduces placental perfusion and causes placental dysfunction, but the one or more causes of shallow placental invasion are unknown. We hypothesized that infection with adeno-associated virus-2 (AAV-2) inhibits trophoblast invasion and is associated with preeclampsia, which is a common obstetric complication resulting from placental dysfunction. We determined that transformed extravillous trophoblast (HTR-8/SVneo) cells were susceptible to AAV-2 infection in the presence or absence of adenovirus, which provides helper function for AAV-2 replication, and that AAV-2 infection reduced invasion of HTR-8/SVneo cells through an extracellular matrix before cytopathic effects were detected. In a case-control study, AAV-2 DNA was found more frequently in trophoblast cells from cases of severe preeclampsia (22/40) than from normal term deliveries (5/27, P = 0.002). These results indicate that AAV-2 infection is a previously unidentified cause of placental dysfunction. Additional studies to determine the susceptibility of extravillous trophoblast to other viruses, and the mechanisms by which viral infection impairs placental function, are warranted.

摘要

绒毛外滋养层细胞对子宫壁的浅侵入会减少胎盘灌注并导致胎盘功能障碍,但胎盘浅侵入的一个或多个原因尚不清楚。我们推测腺相关病毒2(AAV-2)感染会抑制滋养层细胞的侵入,并且与先兆子痫有关,先兆子痫是一种由胎盘功能障碍引起的常见产科并发症。我们确定,无论是否存在腺病毒(腺病毒为AAV-2复制提供辅助功能),转化的绒毛外滋养层(HTR-8/SVneo)细胞均易受AAV-2感染,并且在检测到细胞病变效应之前,AAV-2感染会减少HTR-8/SVneo细胞通过细胞外基质的侵入。在一项病例对照研究中,与正常足月分娩的胎盘滋养层细胞(5/27,P=0.002)相比,重度先兆子痫病例的胎盘滋养层细胞中更频繁地发现AAV-2 DNA(22/40)。这些结果表明,AAV-2感染是胎盘功能障碍先前未被识别的原因。有必要进行进一步的研究,以确定绒毛外滋养层对其他病毒的易感性,以及病毒感染损害胎盘功能的机制。

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