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Subset of DC-SIGN(+) dendritic cells in human blood transmits HIV-1 to T lymphocytes

  • Department of Molecular Cell Biology, Vrÿe Universiteit Medical Center, Amsterdam, The Netherlands.

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The dendritic cell (DC)-specific molecule DC-SIGN is a receptor for the HIV-1 envelope glycoprotein gp120 and is essential for the dissemination of HIV-1. DC-SIGN is expressed by DCs, both monocyte-derived DCs and DCs in several tissues, including mucosa and lymph nodes. To identify a DC-SIGN(+) DC in blood that may be involved in HIV-1 infection through blood, we have analyzed the expression of DC-SIGN in human blood cells. Here we describe the characterization of a subset of DCs in human blood, isolated from T-/NK-/B-cell-depleted peripheral blood mononuclear cells (PBMCs) on the basis of expression of DC-SIGN. This subset coexpresses CD14, CD16, and CD33 and is thus of myeloid origin. In contrast to CD14(+) monocytes, DC-SIGN(+) blood cells display a DC-like morphology and express markers of antigen-presenting cells, including CD1c, CD11b, CD11c, CD86, and high levels of major histocompatibility complex (MHC) class I and II molecules. This DC population differs from other described CD14(-) blood DC subsets. Functionally, DC-SIGN(+) blood DCs are able to stimulate proliferation of allogeneic T cells and can produce tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) upon activation with lipopolysaccharide (LPS). When they encounter HIV-1, low amounts of these blood DC-SIGN(+) DCs enhance infection of T lymphocytes in trans, whereas blood monocytes and CD14(-) blood DCs are not capable of transmitting HIV-1. Therefore DC-SIGN(+) blood DCs can be the first target for HIV-1 upon transmission via blood; they can capture minute amounts of HIV-1 through DC-SIGN and transfer HIV-1 to infect target T cells in trans.

Original languageEnglish
Pages (from-to)1780-6
Number of pages7
JournalBlood
Volume100
Issue number5
DOIs
Publication statusPublished - 1 Sept 2002

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 5 - Gender Equality
    SDG 5 Gender Equality

Keywords

  • Cell Adhesion Molecules
  • Cell Communication/immunology
  • Cell Differentiation/immunology
  • Dendritic Cells/immunology
  • HIV Infections/immunology
  • HIV-1/immunology
  • Humans
  • Lectins/immunology
  • Lectins, C-Type
  • Receptors, Cell Surface/immunology
  • T-Lymphocytes/immunology
  • Viral Proteins/immunology

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