Chemokine receptor CCR5 genotype influences the kinetics of human immunodeficiency virus type 1 infection in human PBL-SCID mice

被引:25
|
作者
Picchio, GR [1 ]
Gulizia, RJ [1 ]
Mosier, DE [1 ]
机构
[1] SCRIPPS RES INST, DEPT IMMUNOL IMM7, LA JOLLA, CA 92037 USA
关键词
D O I
10.1128/JVI.71.9.7124-7127.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Individuals homozygous for a 32-bp deletion (Delta 32) in the CCR5 gene encoding the coreceptor for macrophage-tropic human immunodeficiency virus type 1 (HIV-1) are resistant to virus infection, and heterozygous individuals show some slowing of disease progression. The impact of the CCR5 genotype on HIV-1 infection was assessed in vitro and in the human PBL-SCID (hu-PBL-SCID) model. Cells and hu-PBL-SCID mice from CCR5 Delta 32/Delta 32 donors were resistant to infection with macrophage-tropic HIV-1 and showed slower replication of dual-tropic HIV-1. hu-PBL-SCID mice derived from CCR5 Delta 32/+ heterozygotes showed delayed replication of macrophage-tropic HIV-1 despite a small and variable effect of heterozygosity on viral replication in vitro, The level of CCR5 expression appears to limit replication of macrophage-tropic and dual-tropic HIV-1 strains in vivo.
引用
收藏
页码:7124 / 7127
页数:4
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