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首页> 外文期刊>Clinical infectious diseases >Antiretroviral drug concentrations and HIV RNA in the genital tract of HIV-infected women receiving long-term highly active antiretroviral therapy.
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Antiretroviral drug concentrations and HIV RNA in the genital tract of HIV-infected women receiving long-term highly active antiretroviral therapy.

机译:接受长期高度积极的抗逆转录病毒治疗的HIV感染妇女的生殖道中的抗逆转录病毒药物浓度和HIV RNA。

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摘要

OBJECTIVE: Our objective was to determine antiretroviral drug concentrations and human immunodeficiency virus (HIV) RNA rebound in cervicovaginal fluid (CVF) in relation to blood plasma (BP) in women receiving suppressive highly active antiretroviral therapy (HAART). METHODS: Thirty-four HIV-infected women who had plasma HIV RNA levels < or =80 copies/mL for at least 6 months were enrolled. Sixty-eight paired CVF and BP drug concentrations and HIV RNA levels were determined before and 3-4 h after drug administration. For each woman and antiretroviral drug, the CVF:BP drug concentration ratios before and after drug administration were calculated. The nonparametric Wilcoxon rank sum test was used to determine if these ratios were different from 1.0. RESULTS: Lamivudine (administered to 20 patients) and tenofovir (administered to 16) had significantly higher concentrations in CVF than in BP before drug administration, with mean CVF:BP concentration ratios of 3.19 (95% confidence interval, 1.2-8.5) and 5.2(95% confidence interval, 1.2-22.6), respectively. Efavirenz (administered to 13 patients) and lopinavir (administered to 6) had significantly lower concentrations in CVF, with mean CVF:BP concentration ratios of 0.01 (95% confidence interval, 0.00-0.03) and 0.03 (0.01-0.11), respectively. During the study visit (median time after enrollment, 6 months), BP and CVF detectable HIV RNA levels were observed 7 patients (20.6%) and 1 patient (2.9%), respectively. CONCLUSION: Despite lower CVF concentrations of key HAART components, such as efavirenz and lopinavir, virologic rebound was rare. The high concentrations of tenofovir and lamivudine in CVF may have implications for the prevention of sexual transmission during HAART and for pre-exposure or postexposure prophylaxis.
机译:目的:我们的目的是确定接受抑制性高效抗逆转录病毒治疗(HAART)的女性宫颈阴道液(CVF)中抗逆转录病毒药物的浓度和人血浆中的血浆(BP)的人类免疫缺陷病毒(HIV)RNA反弹。方法:招募了34名HIV感染的妇女,这些妇女的血浆HIV RNA水平<或= 80拷贝/ mL,持续至少6个月。在给药前和给药后3-4小时测定了六十八对CVF和BP药物浓度以及HIV RNA水平。对于每种妇女和抗逆转录病毒药物,计算给药前后的CVF:BP药物浓度比。使用非参数Wilcoxon秩和检验确定这些比率是否不同于1.0。结果:拉米夫定(20例患者)和替诺福韦(16例)的CVF浓度显着高于药物治疗前的BP,平均CVF:BP浓度比为3.19(95%置信区间1.2-8.5)和5.2。 (95%置信区间1.2-22.6)。依法韦仑(13例患者)和洛匹那韦(6例患者)的CVF浓度显着降低,平均CVF:BP浓度比分别为0.01(95%置信区间,0.00-0.03)和0.03(0.01-0.11)。在研究访问期间(入组后中位时间为6个月),分别观察到BP和CVF可检测到的HIV RNA水平为7例患者(20.6%)和1例患者(2.9%)。结论:尽管依法韦仑和洛匹那韦等关键HAART组分的CVF浓度较低,但病毒学反弹却很少。 CVF中高浓度的替诺福韦和拉米夫定可能对预防HAART期间的性传播以及接触前或接触后的预防有影响。

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