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HLA - B*57+精英抑制者中CD8+ T细胞对人类免疫缺陷病毒1型nef基因介导的选择性压力的证据。

Evidence of CD8+ T-cell-mediated selective pressure on human immunodeficiency virus type 1 nef in HLA-B*57+ elite suppressors.

作者信息

Bailey Justin R, Brennan Timothy P, O'Connell Karen A, Siliciano Robert F, Blankson Joel N

机构信息

Broadway Research Bldg., Rm. 880, Johns Hopkins University School of Medicine, 733 N. Broadway, Baltimore, MD 21205, USA.

出版信息

J Virol. 2009 Jan;83(1):88-97. doi: 10.1128/JVI.01958-08. Epub 2008 Oct 22.

Abstract

Elite suppressors (ES) are human immunodeficiency virus type 1 (HIV-1)-infected patients who maintain viral loads of <50 copies/ml without treatment. The observation that the HLA-B57 allele is overrepresented in these patients implies that HIV-1-specific CD8(+) T cells play a key role in suppressing viral replication. We have previously shown that while CD8(+) T-cell escape mutations are rarely seen in proviral Gag sequences in resting CD4(+) T cells from peripheral blood, they are present in every clone amplified from the low levels of free virus in the plasma of HLA-B57(+) ES. In this study, we compared the pattern of mutations in Nef sequences amplified from peripheral blood CD4(+) T cells and from plasma virus. We show that Nef mutations are present in plasma virus but are rare in the cellular sequences and provide evidence that these plasma Nef variants represent novel escape mutants. The results provide further evidence of CD8(+) T-cell-mediated selective pressure on plasma virus in ES and suggest that there must be ongoing HIV-1 replication in spite of the very low viral loads seen for these patients.

摘要

精英抑制者(ES)是未经治疗但病毒载量维持在<50拷贝/毫升的1型人类免疫缺陷病毒(HIV-1)感染患者。这些患者中HLA-B57等位基因的比例过高这一观察结果表明,HIV-1特异性CD8(+) T细胞在抑制病毒复制中起关键作用。我们之前已经表明,虽然在外周血静止CD4(+) T细胞的前病毒Gag序列中很少见到CD8(+) T细胞逃逸突变,但在从HLA-B57(+) ES血浆中低水平游离病毒扩增的每个克隆中都存在这种突变。在本研究中,我们比较了从外周血CD4(+) T细胞和血浆病毒中扩增的Nef序列的突变模式。我们发现血浆病毒中存在Nef突变,但在细胞序列中很少见,并提供证据表明这些血浆Nef变体代表新的逃逸突变体。这些结果进一步证明了ES中CD8(+) T细胞对血浆病毒的选择性压力,并表明尽管这些患者的病毒载量非常低,但HIV-1肯定仍在持续复制。

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