122
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Initial Events in Establishing Vaginal Entry and Infection by Human Immunodeficiency Virus Type-1

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          Understanding the initial events in the establishment of vaginal human immunodeficiency virus type-1 (HIV-1) entry and infection has been hampered by the lack of appropriate experimental models. Here, we show in an ex vivo human organ culture system that upon contact in situ, HIV-1 rapidly penetrated both intraepithelial vaginal Langerhans and CD4 + T cells. HIV-1 entered CD4 + T cells almost exclusively by CD4 and CCR5 receptor-mediated direct fusion, without requiring passage from Langerhans cells, and overt productive infection ensued. By contrast, HIV-1 entered CD1a + Langerhans cells primarily by endocytosis, by means of multiple receptors, and virions persisted intact within the cytoplasm for several days. Our findings shed light on the very earliest steps of mucosal HIV infection in vivo and may guide the design of effective strategies to block local transmission and prevent HIV-1 spread.

          Related collections

          Most cited references31

          • Record: found
          • Abstract: found
          • Article: not found

          Human immunodeficiency virus type 1 spinoculation enhances infection through virus binding.

          The study of early events in the human immunodeficiency virus type 1 (HIV-1) life cycle can be limited by the relatively low numbers of cells that can be infected synchronously in vitro. Although the efficiency of HIV-1 infection can be substantially improved by centrifugal inoculation (spinoculation or shell vial methods), the underlying mechanism of enhancement has not been defined. To understand spinoculation in greater detail, we have used real-time PCR to quantitate viral particles in suspension, virions that associate with cells, and the ability of those virions to give rise to reverse transcripts. We report that centrifugation of HIV-1(IIIB) virions at 1,200 x g for 2 h at 25 degrees C increases the number of particles that bind to CEM-SS T-cell targets by approximately 40-fold relative to inoculation by simple virus-cell mixing. Following subsequent incubation at 37 degrees C for 5 h to allow membrane fusion and uncoating to occur, the number of reverse transcripts per target cell was similarly enhanced. Indeed, by culturing spinoculated samples for 24 h, approximately 100% of the target cells were reproducibly shown to be productively infected, as judged by the expression of p24(gag). Because the modest g forces employed in this procedure were found to be capable of sedimenting viral particles and because CD4-specific antibodies were effective at blocking virus binding, we propose that spinoculation works by depositing virions on the surfaces of target cells and that diffusion is the major rate-limiting step for viral adsorption under routine in vitro pulsing conditions. Thus, techniques that accelerate the binding of viruses to target cells not only promise to facilitate the experimental investigation of postentry steps of HIV-1 infection but should also help to enhance the efficacy of virus-based genetic therapies.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Recruitment of HIV and its receptors to dendritic cell-T cell junctions.

            Monocyte-derived dendritic cells (MDDCs) can efficiently bind and transfer HIV infectivity without themselves becoming infected. Using live-cell microscopy, we found that HIV was recruited to sites of cell contact in MDDCs. Analysis of conjugates between MDDCs and T cells revealed that, in the absence of antigen-specific signaling, the HIV receptors CD4, CCR5, and CXCR4 on the T cell were recruited to the interface while the MDDCs concentrated HIV to the same region. We propose that contact between dendritic cells and T cells facilitates transmission of HIV by locally concentrating virus, receptor, and coreceptor during the formation of an infectious synapse.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Sexual transmission and propagation of SIV and HIV in resting and activated CD4+ T cells.

              In sexual transmission of simian immunodeficiency virus, and early and later stages of human immunodeficiency virus-type 1 (HIV-1) infection, both viruses were found to replicate predominantly in CD4(+) T cells at the portal of entry and in lymphoid tissues. Infection was propagated not only in activated and proliferating T cells but also, surprisingly, in resting T cells. The infected proliferating cells correspond to the short-lived population that produces the bulk of HIV-1. Most of the HIV-1-infected resting T cells persisted after antiretroviral therapy. Latently and chronically infected cells that may be derived from this population pose challenges to eradicating infection and developing an effective vaccine.
                Bookmark

                Author and article information

                Contributors
                Journal
                Immunity
                Immunity
                Cell Press
                1074-7613
                1097-4180
                23 February 2007
                23 February 2007
                : 26
                : 2
                : 257-270
                Affiliations
                [1 ]Program in Infectious Diseases, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
                [2 ]Department of Obstetrics and Gynecology, University of Washington School of Medicine, Seattle, WA 98195, USA
                [3 ]Department of Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA
                [4 ]Department of Laboratory Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA
                [5 ]Department of Pathobiology, University of Washington School of Medicine, Seattle, WA 98195, USA
                Author notes
                []Corresponding author jmcelrat@ 123456fhcrc.org
                Article
                IMMUNI1162
                10.1016/j.immuni.2007.01.007
                1885958
                17306567
                4aff86b9-f81b-4412-8d43-42362ffaa14c
                © 2007 ELL & Excerpta Medica.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 24 July 2006
                : 8 November 2006
                : 2 January 2007
                Categories
                Article

                Immunology
                humdisease,cellimmuno,microbio
                Immunology
                humdisease, cellimmuno, microbio

                Comments

                Comment on this article