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DC-SIGN (CD209) mediates dengue virus infection of human dendritic cells

  • Boonrat Tassaneetrithep
  • , Timothy H. Burgess
  • , Angela Granelli-Piperno
  • , Christine Trumpfheller
  • , Jennifer Finke
  • , Wellington Sun
  • , Michael A. Eller
  • , Kovit Pattanapanyasat
  • , Suttipant Sarasombath
  • , Deborah L. Birx
  • , Ralph M. Steinman
  • , Sarah Schlesinger
  • , Mary A. Marovich*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

771 Scopus citations

Abstract

Dengue virus is a single-stranded, enveloped RNA virus that productively infects human dendritic cells (DCs) primarily at the immature stage of their differentiation. We now find that all four serotypes of dengue use DC-SIGN (CD209), a C-type lectin, to infect dendritic cells. THP-1 cells become susceptible to dengue infection after transfection of DC-specific ICAM-3 grabbing nonintegrin (DC-SIGN), or its homologue L-SIGN, whereas the infection of dendritic cells is blocked by anti-DC-SIGN antibodies and not by antibodies to other molecules on these cells. Viruses produced by dendritic cells are infectious for DC-SIGN- and L-SIGN-bearing THP-1 cells and other permissive cell lines. Therefore, DC-SIGN may be considered as a new target for designing therapies that block dengue infection.

Original languageEnglish
Pages (from-to)823-829
Number of pages7
JournalJournal of Experimental Medicine
Volume197
Issue number7
DOIs
StatePublished - Apr 2003

Keywords

  • Antigen-presenting cells
  • Flavivirus
  • Lectin
  • Receptor
  • Virus receptor

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