胎盘中人巨细胞病毒感染及其与胎儿生长受限的关系的回顾性免疫组织化学分析。

Yusuke Funato, Yuki Higashimoto, Yoshiki Kawamura, Yoshiko Sakabe, Minori Iwakura, Masaru Ihira, Kazuya Shiogama, Masafumi Miyata, Haruki Nishizawa, Takao Sekiya, Takuma Fujii, Isao Kosugi, Tetsushi Yoshikawa
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引用次数: 0

摘要

目的:胎儿巨细胞病毒(HCMV)感染可能与胎儿生长受限(FGR)有关。产妇血清状况和先天性HCMV感染的流行受各种因素的影响,如社会经济地位和种族。因此,应检查每个地区先天性hcmv相关FGR的患病率。方法:对2012年1月至2017年1月在藤田保健大学医院分娩的78例FGR患者进行研究。21例非fgr病例作为对照组。从FGR和对照病例中获得的胎盘切片用两种一抗进行免疫染色,以检测即时早期抗原。结果:排除了19例其他病因的FGR患者的胎盘样本。最后,59例病因不明的FGR患者的胎盘标本被纳入病理分析。59份胎盘标本中有4份(6.8%)HCMV抗原阳性。4例阳性病例均采用M0854抗体染色,MAB810R抗体未见阳性。hcmv阳性和阴性FGR病例的母婴临床特征均无差异。病理检查显示血肿3 / 4,梗塞2 / 4。结论:病因不明的FGR胎盘标本中检出HCMV抗原的比例为6.8%。没有显著的产妇或新生儿临床特征来区分hcmv相关的FGR与其他原因引起的FGR。血管炎和炎症可能在hcmv相关FGR的发病机制中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Retrospective immunohistochemical analysis of human cytomegalovirus infection in the placenta and its association with fetal growth restriction.

Retrospective immunohistochemical analysis of human cytomegalovirus infection in the placenta and its association with fetal growth restriction.

Objectives: Fetal human cytomegalovirus (HCMV) infection might be involved in fetal growth restriction (FGR). Maternal serostatus and the prevalence of congenital HCMV infection are affected by various factors, such as socioeconomic status and ethnicity. Therefore, the prevalence of congenital HCMV-related FGR should be examined in each region.

Methods: Seventy-eight cases of FGR with delivery between January 2012 and January 2017 at Fujita Health University Hospital were studied. Twenty-one non-FGR cases were also included as a control group. Placental sections obtained from the FGR and control cases were immunostained with two primary antibodies for detecting immediate early antigens.

Results: Nineteen placental samples from FGR cases with another etiology were excluded. Finally, 59 placental samples from FGR cases of unknown etiology were included in the pathological analysis. Four of 59 (6.8%) placental samples were positive for HCMV antigen. All four positive cases were stained with the M0854 antibody, and there were no positive case with the MAB810R antibody. Neither maternal nor infantile clinical features were different between the HCMV-positive and -negative FGR cases. A pathological examination showed a hematoma in three of four cases and infarction in two of four cases.

Conclusions: HCMV antigen was detected in 6.8% of placental samples obtained from FGR cases without an obvious etiology. No remarkable maternal or neonatal clinical features discriminated HCMV-related FGR from FGR due to other causes. Vasculitis and inflammation might play important roles in the pathogenesis of HCMV-related FGR.

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