| Literature DB >> 32188724 |
Fernando Real1,2,3, Claude Capron4, Alexis Sennepin1,2,3, Riccardo Arrigucci5, Aiwei Zhu1,2,3, Gérémy Sannier1,2,3, Jonathan Zheng1,2,3, Lin Xu1,2,3, Jean-Marc Massé2,3,6, Ségolène Greffe7, Michelle Cazabat8, Maribel Donoso9, Pierre Delobel10,11,12, Jacques Izopet8,10,11, Eliseo Eugenin9, Maria Laura Gennaro5, Elisabeth Rouveix7, Elisabeth Cramer Bordé1,2,4, Morgane Bomsel13,2,3.
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.Entities:
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Year: 2020 PMID: 32188724 DOI: 10.1126/scitranslmed.aat6263
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956