Geijtenbeek T B, Kwon D S, Torensma R, van Vliet S J, van Duijnhoven G C, Middel J, Cornelissen I L, Nottet H S, KewalRamani V N, Littman D R, Figdor C G, van Kooyk Y
Department of Tumor Immunology, University Medical Center St. Radboud, Nijmegen, The Netherlands.
Cell. 2000 Mar 3;100(5):587-97. doi: 10.1016/s0092-8674(00)80694-7.
Dendritic cells (DC) capture microorganisms that enter peripheral mucosal tissues and then migrate to secondary lymphoid organs, where they present these in antigenic form to resting T cells and thus initiate adaptive immune responses. Here, we describe the properties of a DC-specific C-type lectin, DC-SIGN, that is highly expressed on DC present in mucosal tissues and binds to the HIV-1 envelope glycoprotein gp120. DC-SIGN does not function as a receptor for viral entry into DC but instead promotes efficient infection in trans of cells that express CD4 and chemokine receptors. We propose that DC-SIGN efficiently captures HIV-1 in the periphery and facilitates its transport to secondary lymphoid organs rich in T cells, to enhance infection in trans of these target cells.
树突状细胞(DC)捕获进入外周黏膜组织的微生物,然后迁移至二级淋巴器官,在那里它们将这些微生物以抗原形式呈递给静止的T细胞,从而启动适应性免疫反应。在此,我们描述了一种DC特异性C型凝集素DC-SIGN的特性,它在黏膜组织中的DC上高度表达,并与HIV-1包膜糖蛋白gp120结合。DC-SIGN并非作为病毒进入DC的受体发挥作用,而是促进表达CD4和趋化因子受体的细胞发生反式高效感染。我们提出,DC-SIGN在外周有效捕获HIV-1,并促进其转运至富含T细胞的二级淋巴器官,以增强这些靶细胞的反式感染。