免疫测定和分子方法研究cART感染HIV患者外周血单个核细胞DNA甲基化变化

A. Roșca, G. Anton, L. Ene, I. Iancu, A. Temereanca, C. Achim, S. Ruță
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引用次数: 7

摘要

本研究旨在探讨抗逆转录病毒治疗对一组重度治疗的HIV感染者甲基化标志物的影响。使用免疫和分子方法研究了从抗逆转录病毒感染患者和健康对照者收集的外周血单个核细胞中分离的DNA甲基化谱的潜在变化。5-甲基胞嘧啶百分比与病毒前DNA和活跃复制呈负相关,而DNMT1 (p = 0.01)和DNMT3A (p = 0.004)与病毒活跃复制独立相关。DNMT3A表达随着总治疗时间(p = 0.03)、曾经使用过的抗逆转录病毒药物数量(p = 0.003)和蛋白酶抑制剂的累积暴露(p = 0.02)而增加,即使在目前未检测到HIV的患者中也是如此。
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Immunoassay and molecular methods to investigate DNA methylation changes in peripheral blood mononuclear cells in HIV infected patients on cART
ABSTRACT This study aimed to investigate the influence of antiretroviral therapy on methylation markers, in a group of HIV infected, heavily treated patients. Immune and molecular methods were used to investigate potential changes in methylation profile in DNA isolated from peripheral blood mononuclear cells collected from antiretroviral-experienced HIV infected patients and healthy controls. The percentage of 5-methylcytosine was inversely correlated with proviral DNA and active replication while DNMT1 (p = 0.01) and DNMT3A (p = 0.004) independently correlated with active viral replication. DNMT3A expression increased with total treatment duration (p = 0.03), number of antiretroviral drugs ever used (p = 0.003), and cumulative exposure to protease inhibitors (p = 0.02) even in currently HIV undetectable patients.
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