Emergence and persistence of CXCR4-tropic HIV-1 in a population of men from the Multicenter AIDS Cohort Study

被引:76
作者
Shepherd, James C. [1 ,3 ]
Jacobson, Lisa P. [2 ]
Qiao, Wei [2 ]
Jamieson, Beth D. [5 ]
Phair, John P. [6 ,7 ]
Piazza, Paolo [8 ]
Quinn, Thomas C. [1 ,4 ]
Margolick, Joseph B. [2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Baltimore, MD 21218 USA
[3] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[4] NIAID, Bethesda, MD 20892 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[6] Northwestern Univ, Howard Brown Hlth Ctr, Chicago, IL 60611 USA
[7] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[8] Univ Pittsburgh, Grad Sch Publ Hlth, Pittsburgh, PA USA
关键词
D O I
10.1086/591623
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We examined the emergence of CXCR4 (i.e., X4) tropism in 67 male human immunodeficiency virus type 1 (HIV-1) seroconverters from the Multicenter AIDS Cohort Study (MACS) who were selected to reflect the full spectrum of rates of HIV-1 disease progression. A mean of 10 serial samples per donor were evaluated by a laboratory-validated, commercially available assay to determine phenotypic coreceptor use. A total of 52% of men had dual-or mixed-tropic HIV-1 detected at 1 or more of the time points tested. Use of X4 by HIV-1 was detected more frequently among men who developed AIDS (defined as a CD4(+) T cell count of < 200 cells/mu L and/or an AIDS-defining illness) <= 11 years after seroconversion than among those who did not ( P=.005), as well as among men who exhibited a total T cell count decline (i.e., a CD3(+) inflection point), compared with those who did not (P=.03). For men in whom both X4 virus and an inflection point were detected, emergence of X4 virus preceded the inflection point by a median of 0.83 years. The median CD4(+) T cell count at first detection of X4 viruses before the onset of AIDS was 475 cells/mu L. We conclude that HIV-1 variants that used X4 frequently emerged at high CD4(+) T cell counts and may contribute to the decrease in T cell numbers during late HIV-1 infection.
引用
收藏
页码:1104 / 1112
页数:9
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