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HIV-1 co-receptor expression on trophoblastic cells from early placentas and permissivity to infection by several HIV-1 primary isolates

机译:早期胎盘滋养层细胞上HIV-1共受体表达以及几种HIV-1主要分离株对感染的容许性

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摘要

We examined CD4 and major HIV-1 co-receptor expression by trophoblast cells (TC) from early placentas, and the permissiveness of TC for infection by several natural HIV-1 isolates in vitro. Ten early placentas (4–6 weeks of gestation) from HIV− women were obtained after elective abortion. CD4 and HIV-1 co-receptor expression by TC was examined in terms of both mRNA and protein. The same TC were then challenged with three clinical HIV isolates of known phenotype, two originating from mothers who transmitted the virus to their child and one from a vertically infected newborn. TC infection was detected by polymerase chain reaction. CD4 expression was detected in five of the 10 placentas, while membrane protein expression of CCR3, CXCR4 and CCR5 was detected in every case, despite quantitative differences among individuals. Bonzo, GPR1 and ChemR23 mRNAs were detected in all TC preparations. TC from seven out of eight placentas were permissive to HIV entry, but no productive viral replication was detected (reverse transcriptase activity in culture supernatants). Interestingly, the addition of chemokine(s) or a CD4-blocking antibody to the cultures failed to inhibit TC virus entry. These data point to marked interindividual variability in HIV co-receptor expression by trophoblast cells and show that TC from early placentas can be infected in vitro by clinical HIV-1 isolates. They also suggest that viral entry in vitro might occur through a mechanism independent of both CD4 and chemokine receptors.
机译:我们检查了来自早期胎盘的滋养层细胞(TC)的CD4和主要HIV-1共受体表达,以及TC在体外被几种天然HIV-1分离株感染的允许性。选择性流产后,从艾滋病毒感染者中获得了十个早期胎盘(妊娠4-6周)。 TC检验了CD4和HIV-1共受体的mRNA和蛋白表达。然后,用3个已知表型的临床HIV分离株对同一TC进行攻击,其中2个源于将病毒传播给孩子的母亲,另一个来自垂直感染的新生儿。通过聚合酶链反应检测TC感染。尽管个体之间存在定量差异,但在10个胎盘中有5个检测到CD4表达,而在每种情况下均检测到CCR3,CXCR4和CCR5的膜蛋白表达。在所有TC制剂中均检测到Bonzo,GPR1和ChemR23 mRNA。八分之九的胎盘中的TC允许进入HIV,但未检测到有效的病毒复制(培养物上清液中的逆转录酶活性)。有趣的是,向培养物中添加趋化因子或CD4阻断抗体未能抑制TC病毒的进入。这些数据表明滋养层细胞在HIV共受体表达中存在明显的个体差异,并表明早期胎盘的TC可以在体外被临床HIV-1分离株感染。他们还暗示体外病毒进入可能通过独立于CD4和趋化因子受体的机制发生。

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