Immunodeficiency virus uptake, turnover, and 2-phase transfer in human dendritic cells

Stuart Turville(The University of Melbourne), John J. Santos(The University of Melbourne), Ines Frank(The University of Melbourne), Paul Cameron(The University of Melbourne), John Wilkinson(The University of Melbourne), Monica Miranda‐Saksena(The University of Melbourne), Joanne Dable(The University of Melbourne), Hella Stössel(The University of Melbourne), Nikolaus Romani(The University of Melbourne), Michael Piatak(The University of Melbourne), Jeffrey D. Lifson(The University of Melbourne), Melissa Pope(The University of Melbourne), Anthony L. Cunningham(The University of Melbourne)
Blood
November 25, 2003
Cited by 391Open Access
Full Text

Abstract

HIV-1 subverts antigen processing in dendritic cells (DCs) resulting in viral uptake, infection, and transfer to T cells. Although DCs bound monomeric gp120 and HIV-1 similarly, virus rarely colocalized with endolysosomal markers, unlike gp120, suggesting HIV-1 alters endolysosomal trafficking. Virus within DC intracellular compartments rapidly moved to DC-CD4+ lymphocyte synapses when introduced to CD4+ lymphocyte cultures. Although viral harboring and transfer from nonlysosomal compartments was transient, given DC-associated virus protein, nucleic acids, and infectious HIV-1 transfer to CD4+, lymphocytes decayed within 24 hours. However a second long-term transfer phase was apparent in immature DCs after 48 hours as a zidovudine-sensitive rise in proviral DNA. Therefore, DCs transfer HIV-1 to CD4+ lymphocytes in 2 distinct phases. Immature and mature DCs first divert virus from the endolysosomal pathway to the DC-T-cell synapse. Secondly, the later transfer phase from immature DCs is through de novo HIV-1 production. Thus, the controversy of DCs being infected or not infected for the mechanics of viral transfer to CD4+ lymphocytes can be addressed as a function of time.


Related Papers

No related papers found

Powered by citation graph analysis