Expression and its clinical significance of HLA-G in HCMV-infected placental villi at early pregnant stage

Objective:To study the expression and its clinical significance of HLA-G in HCMV intrauterine infected placental villi at early pregnant stage. Methods:PCR (polymerase chain reaction) was used to screen the peripheral blood for HCMV-DNA in 462 women who had willingly undergone induced abortion. Then...

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Published in:Journal of Medical Colleges of PLA Vol. 22; no. 1; pp. 31 - 35
Main Author: 张欣文 李芬 盛秋 于学文 任永惠 李学成
Format: Journal Article
Language:English
Published: Maternal and Child Health Center,First Affiliated Hospital of Medical College,Xi'an Jiaotong University,Xi'an 710061,China 01-02-2007
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Summary:Objective:To study the expression and its clinical significance of HLA-G in HCMV intrauterine infected placental villi at early pregnant stage. Methods:PCR (polymerase chain reaction) was used to screen the peripheral blood for HCMV-DNA in 462 women who had willingly undergone induced abortion. Then immunohistochemistry was also used to detect expressions of mouse anti-HCMV early antigen (HCMV-EA) and mouse anti-HLA-G in HCMV-DNA positive cases' placental villi. The difference of HLA-G expressions between the intrauterine infection group(HCMV-EA positives), the intrauterine infection-free group(HCMV-EA negatives) and the normal control group (50 cases of healthy early placental villi) was compared. Results: Of the 78 cases, which were detected HCMV-DNA positive, 11 (14.10%) were HCMV-EA positive. Compared with the other two groups, HLA-G expressions in the intrauterine infection group were both obviously decreased(both P〈0. 001). HLA-G expression positions in all three groups were mainly located in the cytotrophoblast. Conclusion:Intrauterine HCMV infection at early pregnant stage is closely related to HLA-G expression at the maternal-fetal interface. The virogenetic products may affect the expression of HLA-G at the maternal-fetal interface and that of its immunological function, thus leading to different clinical outcomes.
Bibliography:intrauterine infection
human cytomegalovirus; intrauterine infection; HLA-G; maternal-fetal interface
maternal-fetal interface
human cytomegalovirus
HLA-G
31-1002/R
R714.251
ISSN:1000-1948
DOI:10.1016/S1000-1948(07)60007-0