Portal de Periódicos da CAPES

Th17 Cells Are Preferentially Infected Very Early after Vaginal Transmission of SIV in Macaques

2016; Cell Press; Volume: 19; Issue: 4 Linguagem: Inglês

10.1016/j.chom.2016.03.005

1934-6069

Daniel J. Stieh, Edgar Matias, Huanbin Xu, Angela J. Fought, James Blanchard, Preston A. Marx, Ronald S. Veazey, Thomas J. Hope,

Immune Cell Function and Interaction

The difficulty in detecting rare infected cells immediately after mucosal HIV transmission has hindered our understanding of the initial cells targeted by the virus. Working with the macaque simian immunodeficiency virus (SIV) vaginal challenge model, we developed methodology to identify discrete foci of SIV (mac239) infection 48 hr after vaginal inoculation. We find infectious foci throughout the reproductive tract, from labia to ovary. Phenotyping infected cells reveals that SIV has a significant bias for infection of CCR6+ CD4+ T cells. SIV-infected cells expressed the transcriptional regulator RORγt, confirming that the initial target cells are specifically of the Th17 lineage. Furthermore, we detect host responses to infection, as evidenced by apoptosis, cell lysis, and phagocytosis of infected cells. Thus, our analysis identifies Th17-lineage CCR6+ CD4+ T cells as primary targets of SIV during vaginal transmission. This opens new opportunities for interventions to protect these cells and prevent HIV transmission.