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

B Tassaneetrithep, TH Burgess… - The Journal of …, 2003 - rupress.org
B Tassaneetrithep, TH Burgess, A Granelli-Piperno, C Trumpfheller, J Finke, W Sun…
The Journal of experimental medicine, 2003rupress.org
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 …
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.
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