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APOBEC3G levels predict rates of progression to AIDS
被引:25
作者:

Jin, Xia
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机构: Univ Rochester, Dept Med, Rochester, NY 14642 USA

Wu, Hulin
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机构: Univ Rochester, Dept Med, Rochester, NY 14642 USA

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机构:
机构:
[1] Univ Rochester, Dept Med, Rochester, NY 14642 USA
[2] Univ Rochester, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[3] Univ Rochester, Dept Biostat & Computat Biol, Rochester, NY 14642 USA
[4] Univ Rochester, Dept Biochem & Biophys, Rochester, NY 14642 USA
来源:
关键词:
LONG-TERM SURVIVORS;
RESTRICTS HIV-1 INFECTION;
MESSENGER-RNA LEVELS;
CD4(+) T-CELLS;
DISEASE PROGRESSION;
VIRUS-REPLICATION;
TRIM5-ALPHA;
HLA;
PROLIFERATION;
HYPERMUTATION;
D O I:
10.1186/1742-4690-4-20
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Background: APOBEC3G ( hA3G) is a newly discovered cellular factor of innate immunity that inhibits HIV replication in vitro. Whether hA3G conferrs protection against HIV in vivo is not known. To investigate the possible anti-HIV activity of hA3G in vivo, we examined hA3G mRNA abundance in primary human cells isolated from either HIV-infected or HIV-uninfected individuals, and found that hA3G mRNA levels follow a hierarchical order of long-term nonprogressors > HIV-uninfected > Progressors; and, hA3G mRNA abundance is correlated with surrogates of HIV disease progression: viral load and CD4 count. Another group later confirmed that HIV-infected subjects have lower hA3G mRNA levels than HIV-uninfected controls, but did not find correlations between hA3G mRNA levels and viral load or CD4 count. These conflicing results indicate that a more comprehensive, conclusive investigation of hA3G expression levels in various patient cohorts is urgently needed.
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