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HIV-1 的表达和诱导型血液生物标志物。

Blood biomarkers of expressed and inducible HIV-1.

机构信息

Division of Infectious Diseases, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Department of Immunology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

出版信息

AIDS. 2018 Mar 27;32(6):699-708. doi: 10.1097/QAD.0000000000001748.

Abstract

OBJECTIVE

To define the relationships between molecular measures of viral persistence in blood (i.e., plasma viremia, cellular HIV-1 DNA, and mRNA) and expressed or inducible virus from resting CD4 T cells of individuals on suppressive antiretroviral therapy.

DESIGN

We compared molecular measurements of HIV-1 in plasma and in uncultured peripheral blood mononuclear cells (PBMCs) to the levels of virions produced by either unstimulated or phorbol myristate acetate and ionomycin (PMA/iono)-stimulated PBMC or resting CD4 T cells from 21 donors on suppressive antiretroviral therapy.

RESULTS

We found that unstimulated virion release from cultured resting CD4 T cells was positively correlated with the levels of plasma viremia in vivo (Spearman rho = 0.67, P = 0.0017). We also found that levels of both cellular HIV-1 DNA and unspliced HIV-1 mRNA per million uncultured PBMC were positively correlated with the levels of inducible virion release from both PMA/iono-stimulated PBMC (total HIV-1 DNA: rho = 0.64, P = 0.0017; unspliced HIV-1 RNA: rho = 0.77, P < 0.001) and PMA/iono-stimulated resting CD4 T cells (total HIV-1 DNA: rho = 0.75, P < 0.001; unspliced HIV-1 RNA: rho = 0.75, P < 0.001).

CONCLUSION

These results show for the first time that there are strong associations between in-vivo measures of HIV-1 persistence and ex-vivo measures of spontaneous and inducible virus production from cultured PBMC and resting CD4 T cells. Findings from this study provide insight into the biology of HIV-1 persistence and suggest methods to guide the evaluation of clinical strategies to reduce the size of the viral reservoir.

摘要

目的

定义血液中病毒持续存在的分子指标(即血浆病毒血症、细胞 HIV-1 DNA 和 mRNA)与接受抑制性抗逆转录病毒治疗个体的静止 CD4 T 细胞中表达或可诱导的病毒之间的关系。

设计

我们比较了 21 名接受抑制性抗逆转录病毒治疗的供体的血浆和未培养外周血单核细胞(PBMC)中的 HIV-1 分子测量值与未刺激或佛波醇肉豆蔻酸乙酯和离子霉素(PMA/iono)刺激的 PBMC 或静止 CD4 T 细胞产生的病毒粒子水平。

结果

我们发现,培养的静止 CD4 T 细胞中未刺激的病毒粒子释放与体内血浆病毒血症水平呈正相关(Spearman rho = 0.67,P = 0.0017)。我们还发现,每百万个未培养的 PBMC 中细胞 HIV-1 DNA 和未剪接的 HIV-1 mRNA 的水平与 PMA/iono 刺激的 PBMC(总 HIV-1 DNA:rho = 0.64,P = 0.0017;未剪接的 HIV-1 RNA:rho = 0.77,P < 0.001)和 PMA/iono 刺激的静止 CD4 T 细胞(总 HIV-1 DNA:rho = 0.75,P < 0.001;未剪接的 HIV-1 RNA:rho = 0.75,P < 0.001)中诱导的病毒粒子释放呈正相关。

结论

这些结果首次表明,体内 HIV-1 持续存在的测量值与从培养的 PBMC 和静止 CD4 T 细胞中自发和诱导产生病毒的体外测量值之间存在很强的关联。这项研究的结果提供了对 HIV-1 持续存在生物学的深入了解,并为评估减少病毒储存库大小的临床策略提供了方法。

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