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Platelets from HIV-infected individuals on antiretroviral drug therapy with poor CD4+ T cell recovery can harbor replication-competent HIV despite viral suppression

  • Fernando Real
  • , Claude Capron
  • , Alexis Sennepin
  • , Riccardo Arrigucci
  • , Aiwei Zhu
  • , Gérémy Sannier
  • , Jonathan Zheng
  • , Lin Xu
  • , Jean Marc Massé
  • , Ségolène Greffe
  • , Michelle Cazabat
  • , Maribel Donoso
  • , Pierre Delobel
  • , Jacques Izopet
  • , Eliseo Eugenin
  • , Maria Laura Gennaro
  • , Elisabeth Rouveix
  • , Elisabeth Cramer Bordé
  • , Morgane Bomsel

Research output: Contribution to journalArticlepeer-review

Abstract

In addition to hemostasis, human platelets have several immune functions and interact with infectious pathogens including HIV in vitro. Here, we report that platelets from HIV-infected individuals on combined antiretroviral drug therapy (ART) with low blood CD4+ T cell counts (<350 cells/μl) contained replication-competent HIV despite viral suppression. In vitro, human platelets harboring HIV propagated the virus to macrophages, a process that could be prevented with the biologic abciximab, an anti-integrin αIIb/β3 Fab. Furthermore, in our cohort, 88% of HIV-infected individuals on ART with viral suppression and with platelets containing HIV were poor immunological responders with CD4+ T cell counts remaining below <350 cells/μl for more than one year. Our study suggests that platelets may be transient carriers of HIV and may provide an alternative pathway for HIV dissemination in HIV-infected individuals on ART with viral suppression and poor CD4+ T cell recovery.

Original languageEnglish (US)
Article numbereaat6263
JournalScience Translational Medicine
Volume12
Issue number535
DOIs
StatePublished - Mar 18 2020

ASJC Scopus subject areas

  • General Medicine

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