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Impact of pre-adapted HIV transmission

机译:预先适应的艾滋病毒传播的影响

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Human leukocyte antigen class I (HLA)-restricted CD8(+) T lymphocyte (CTL) responses are crucial to HIV-1 control. Although HIV can evade these responses, the longer-term impact of viral escape mutants remains unclear, as these variants can also reduce intrinsic viral fitness. To address this, we here developed a metric to determine the degree of HIV adaptation to an HLA profile. We demonstrate that transmission of viruses that are pre-adapted to the HLA molecules expressed in the recipient is associated with impaired immunogenicity, elevated viral load and accelerated CD4(+) T cell decline. Furthermore, the extent of pre-adaptation among circulating viruses explains much of the variation in outcomes attributed to the expression of certain HLA alleles. Thus, viral pre-adaptation exploits 'holes' in the immune response. Accounting for these holes may be key for vaccine strategies seeking to elicit functional responses from viral variants, and to HIV cure strategies that require broad CTL responses to achieve successful eradication of HIV reservoirs.
机译:人类白细胞抗原I类(HLA)限制的CD8(+)T淋巴细胞(CTL)反应对HIV-1控制至关重要。尽管HIV可以逃避这些反应,但是病毒逃逸突变体的长期影响仍不清楚,因为这些变异体也可以降低内在的病毒适应性。为了解决这个问题,我们在这里开发了一种度量标准,以确定HIV对HLA谱图的适应程度。我们证明病毒的传播是预先适应接受者中表达的HLA分子与免疫原性受损,病毒载量升高和CD4(+)T细胞加速下降有关。此外,循环病毒之间的预适应程度可解释许多归因于某些HLA等位基因表达的结果差异。因此,病毒的预适应利用了免疫反应中的“漏洞”。对于寻求从病毒变体引起功能性反应的疫苗策略以及需要广泛CTL反应以成功消除HIV储库的HIV治愈策略而言,考虑这些漏洞可能是关键。

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