4.6 Article

DC-SIGN on B lymphocytes is required for transmission of HIV-1 to T lymphocytes

Journal

PLOS PATHOGENS
Volume 2, Issue 7, Pages 691-704

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.ppat.0020070

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Funding

  1. NCI NIH HHS [R01 CA082053] Funding Source: Medline
  2. NIAID NIH HHS [R37 AI041870, U01 AI035041, R37AI041870] Funding Source: Medline

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Infection of T cells by HIV-1 can occur through binding of virus to dendritic cell (DC)-specific ICAM-3 grabbing nonintegrin (DC-SIGN) on dendritic cells and transfer of virus to CD4(+) T cells. Here we show that a subset of B cells in the blood and tonsils of normal donors expressed DC-SIGN, and that this increased after stimulation in vitro with interleukin 4 and CD40 ligand, with enhanced expression of activation and co-stimulatory molecules CD23, CD58, CD80, and CD86, and CD22. The activated B cells captured and internalized X4 and R5 tropic strains of HIV-1, and mediated trans infection of T cells. Pretreatment of the B cells with anti-DC-SIGN monoclonal antibody blocked trans infection of T cells by both strains of HIV-1. These results indicate that DC-SIGN serves as a portal on B cells for HIV-1 infection of T cells in trans. Transmission of HIV-1 from B cells to T cells through this DC-SIGN pathway could be important in the pathogenesis of HIV-1 infection.

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