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DC-SIGN Is a Receptor for Human Herpesvirus 8 on Dendritic Cells and Macrophages
Author(s) -
Giovanna Rappocciolo,
Frank J. Jenkins,
Heather R. Hensler,
Paolo Piazza,
Mariel Jais,
Luann Borowski,
Simon C. Watkins,
Charles R. Rinaldo
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.176.3.1741
Subject(s) - dc sign , biology , virology , cd8 , dendritic cell , immune system , mannose receptor , virus , primary effusion lymphoma , receptor , immunology , macrophage , biochemistry , in vitro
Human herpesvirus 8 (HHV-8) causes Kaposi's sarcoma and pleural effusion lymphoma. In this study, we show that dendritic cell-specific ICAM-3 grabbing nonintegrin (DC-SIGN; CD209) is a receptor for HHV-8 infection of myeloid DCs and macrophages. DC-SIGN was required for virus attachment to these cells and DC-SIGN-expressing cell lines. HHV-8 binding and infection were blocked by anti-DC-SIGN mAb and soluble DC-SIGN, and mannan, a natural ligand for DC-SIGN. Infection of DCs and macrophages with HHV-8 led to production of viral proteins, with little production of viral DNA, similar to HHV-8 infection of vascular endothelial cells. Infection of DCs resulted in down-regulation of DC-SIGN, a decrease in endocytic activity, and an inhibition of Ag stimulation of CD8+ T cells. We propose that DC-SIGN serves as a portal for immune dysfunction and oncogenesis caused by HHV-8 infection.

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