Rahimzadeh Mahsa, Norouzian Marzieh, Arabpour Fahimeh, Naderi Nadereh
a Department of Biochemistry, Faculty of Medicine , Hormozgan University of Medical Sciences , Bandar Abbas, Iran.
c Molecular Medicine Research Center , Hormozgan University of Medical Sciences , Bandar Abbas , Iran.
Expert Rev Clin Immunol. 2016;12(2):209-27. doi: 10.1586/1744666X.2016.1105740. Epub 2015 Nov 18.
Regulatory T-cells (Tregs) are key players in successful pregnancy and their deficiencies are implicated in pregnancy complications such as preeclampsia (PE), but the results are inconsistent among studies. This study aims to compile an overview of the studies about the associations of Tregs and PE risk and to provide recommendations for future research. A sensitive search of three databases including PubMed, Scopus and Google scholar (from 1995 to January 9, 2015) identified 636 unique titles. An accurate process of study selection, data extraction and method qualification were independently conducted by authors on retrieved papers. Seventeen papers met the inclusion criteria and were included in quality assessment. Regarding the source of Tregs, 14 studies assessed Tregs in peripheral blood, 2 studies in peripheral blood and decidua and one study in peripheral blood and umbilical cord blood. Despite variation in the combinations of markers and other aspects of the studies designs, remarkable constancy in the results of studies that measured Tregs as CD4+FoxP3+ or CD4+CD25+FoxP3+ cells (but not CD4+CD25(high/low)FoxP3+ markers) was found, which in broad terms showed a shift towards fewer Treg cells in PE. This review revealed an association between lower percentage of circulating CD4+FoxP3+ or CD4+CD25+FoxP3+ Tregs and the risk of PE. Given the above issue and regarding the high consistency of studies on reduction of suppressive activity of Tregs in PE, we have proposed a model in which the Tregs deficiency is a reflection of immune endocrine imbalance, which reverses maternal tolerance and results in development of preeclampsia.
调节性T细胞(Tregs)是成功妊娠的关键因素,其功能缺陷与子痫前期(PE)等妊娠并发症有关,但各研究结果并不一致。本研究旨在汇总有关Tregs与PE风险关联的研究综述,并为未来研究提供建议。通过对包括PubMed、Scopus和谷歌学术(1995年至2015年1月9日)在内的三个数据库进行全面检索,共识别出636个独特标题。作者对检索到的论文独立进行了准确的研究筛选、数据提取和方法鉴定过程。17篇论文符合纳入标准并纳入质量评估。关于Tregs的来源,14项研究评估了外周血中的Tregs,2项研究评估了外周血和蜕膜中的Tregs,1项研究评估了外周血和脐带血中的Tregs。尽管研究设计在标志物组合和其他方面存在差异,但在将Tregs测定为CD4+FoxP3+或CD4+CD25+FoxP3+细胞(而非CD4+CD25(高/低)FoxP3+标志物)的研究结果中发现了显著的一致性,从广义上讲,这表明PE中Treg细胞数量减少。本综述揭示了循环中CD4+FoxP3+或CD4+CD25+FoxP3+ Tregs百分比降低与PE风险之间的关联。鉴于上述问题,以及关于PE中Tregs抑制活性降低的研究具有高度一致性,我们提出了一个模型,其中Tregs缺陷是免疫内分泌失衡的反映,这种失衡会逆转母体耐受性并导致子痫前期的发展。