Identification of a major co-receptor for primary isolates of HIV-1

被引:3127
作者
Deng, HK
Liu, R
Ellmeier, W
Choe, S
Unutmaz, D
Burkhart, M
DiMarzio, P
Marmon, S
Sutton, RE
Hill, CM
Davis, CB
Peiper, SC
Schall, TJ
Littman, DR
Landau, NR
机构
[1] NYU,MED CTR,SKIRBALL INST BIOMOL MED,NEW YORK,NY 10016
[2] NYU,MED CTR,HOWARD HUGHES MED INST,NEW YORK,NY 10016
[3] ROCKEFELLER UNIV,AARON DIAMOND AIDS RES CTR,NEW YORK,NY 10016
[4] STANFORD UNIV,MED CTR,DEPT BIOCHEM,STANFORD,CA 94305
[5] UNIV LOUISVILLE,SCH MED,JAMES GRAHAM BROWN CANC CTR,LOUISVILLE,KY 40207
[6] DNAX RES INST MOLEC & CELLULAR BIOL INC,DEPT IMMUNOL,PALO ALTO,CA 94304
关键词
D O I
10.1038/381661a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Entry of HIV-1 into target cells requires cell-surface CD4 and additional host cell cofactors. A cofactor required for infection with virus adapted for growth in transformed T-cell lines was recently identified and named fusin. However, fusin does not promote entry of macrophage-tropic viruses, which are believed to be the key pathogenic strains in vivo. The principal cofactor for entry mediated by the envelope glycoproteins of primary macrophage-tropic strains of HIV-1 is CC-CKR-5, a receptor for the beta-chemokines RANTES, MIP-1 alpha and MIP-1 beta.
引用
收藏
页码:661 / 666
页数:6
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