Abstract

BackgroundThe placenta plays an important role in the control of in utero HIV-1 mother-to-child transmission (MTCT). Proinflammatory cytokines in the placental environment are particularly implicated in this control. We thus investigated the effect of TNF-α on HIV-1 expression in human placental tissues in vitro.ResultsHuman placental chorionic villi fragments were infected with varying doses of luciferase reporter HIV-1 pseudotypes with the R5, X4-Env or the vesicular stomatitis virus protein G (VSV-G). Histocultures were then performed in the presence or absence of recombinant human TNF-α. Luciferase activity was measured at different time points in cell lysates or on whole fragments using ex vivo imaging systems.A significant increase in viral expression was detected in placental fragments infected with 0.2 ng of p24 antigen/fragment (P = 0.002) of VSV-G pseudotyped HIV-1 in the presence of TNF-α seen after 120 hours of culture. A time independent significant increase of viral expression by TNF-α was observed with higher doses of VSV-G pseudotyped HIV-1. When placental fragments were infected with R5-Env pseudotyped HIV-1, a low level of HIV expression at 168 hours of culture was detected for 3 of the 5 placentas tested, with no statistically significant enhancement by TNF-α. Infection with X4-Env pseudotyped HIV-1 did not lead to any detectable luciferase activity at any time point in the absence or in the presence of TNF-α.ConclusionTNF-α in the placental environment increases HIV-1 expression and could facilitate MTCT of HIV-1, particularly in an inflammatory context.

Highlights

  • The placenta plays an important role in the control of in utero human immunodeficiency virus type 1 (HIV-1) mother-to-child transmission (MTCT)

  • It has been observed that transmission of HIV-1 between T lymphocytes and trophoblasts is possible [2,3] and that cell-to-cell contact between HIV-1 infected peripheral blood mononuclear cells (PBMCs) and cells of trophoblast origin led to the passage of virus from the apical to the basolateral side of a trophoblast barrier reconstituted in vitro [4]

  • When placental fragments were infected by the VSV-G pseudotyped HIV-1, a dose dependent replication was observed with an increase of luciferase activity overtime

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Summary

Introduction

The placenta plays an important role in the control of in utero HIV-1 mother-to-child transmission (MTCT). It has been observed that transmission of HIV-1 between T lymphocytes and trophoblasts is possible [2,3] and that cell-to-cell contact between HIV-1 infected peripheral blood mononuclear cells (PBMCs) and cells of trophoblast origin led to the passage of virus from the apical to the basolateral side of a trophoblast barrier reconstituted in vitro [4]. Soluble factors such as RANTES and MIP-lβ decrease viral passage through this placental trophoblast barriers inoculated with HIV-1 infected cells while TNF-α and IL-8 increase it [5].

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