Dendritic cells express multiple chemokine receptors used as coreceptors for HIV entry

被引:0
|
作者
Rubbert, A
Combadiere, C
Ostrowski, M
Arthos, J
Dybul, M
Machado, E
Cohn, MA
Hoxie, JA
Murphy, PM
Fauci, AS
Weissman, D
机构
[1] NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Host Def Lab, NIH, Bethesda, MD 20892 USA
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
来源
JOURNAL OF IMMUNOLOGY | 1998年 / 160卷 / 08期
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中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cells of the dendritic lineage are thought to be among the first cells infected after mucosal exposure to HIV, Zn this study, we have identified the presence of multiple chemokine receptors on dendritic cells (DC) that may function as coreceptors for HIV entry, DC effectively used CCR5 far entry of macrophage (M)-tropic isolates. CCR3, the eotaxin receptor, initially identified on eosinophils, is expressed on DC and may be used as an entry coreceptor by certain dual-tropic strains, CXCR4 was not expressed on DC, although SDF-1 induced a calcium flux and DC could be infected by T cell line (T)-tropic HIV. Our findings pro,ide evidence for the presence of a non-CXCR4 SDF-1 receptor on DC that is used mainly by T-tropic strains of HIV. DC from individuals homozygous for a 32-bp deletion of the CCR5 gene are also infectable with M-tropic strains of HIV-1, and this infection is inhibited by stromal cell-derived factor (SDF)1, suggesting that this receptor can also be used by hi-tropic HIV for entry, Delineation of the spectrum of coreceptor usage on DC may offer new approaches to interfere with the initiation and propagation of HIV infection.
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页码:3933 / 3941
页数:9
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