HIV-1 entry into CD4 + cells is mediated by the chemokine receptor CC-CKR-5

The β-chemokines MIP-1α, MIP-1β and RANTES inhibit infection of CD4 + cells by primary, non-syncytium-inducing (NSI) HIV-1 strains at the virus entry stage, and also block env -mediated cell–cell membrane fusion. CD4 + T cells from some HIV-1-exposed uninfected individuals cannot fuse with NSI HIV-1...

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Veröffentlicht in:Nature (London) 1996-06, Vol.381 (6584), p.667-673
Hauptverfasser: Dragic, Tatjana, Litwin, Virginia, Allaway, Graham P, Martin, Scott R, Huang, Yaoxing, Nagashima, Kirsten A, Cayanan, Charmagne, Maddon, Paul J, Koup, Richard A, Moore, John P, Paxton, William A
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Sprache:eng
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Zusammenfassung:The β-chemokines MIP-1α, MIP-1β and RANTES inhibit infection of CD4 + cells by primary, non-syncytium-inducing (NSI) HIV-1 strains at the virus entry stage, and also block env -mediated cell–cell membrane fusion. CD4 + T cells from some HIV-1-exposed uninfected individuals cannot fuse with NSI HIV-1 strains and secrete high levels of β-chemokines. Expression of the β-chemokine receptor CC-CKR-5 in CD4 + , non-permissive human and non-human cells renders them susceptible to infection by NSI strains, and allows env -mediated membrane fusion. CC-CKR-5 is a second receptor for NSI primary viruses.
ISSN:0028-0836
1476-4687
DOI:10.1038/381667a0