Behavioral and Biomedical Research Department, Family Health International, Research Triangle Park, NC 27709, USA.
AIDS. 2010 Feb 20;24(4):573-82. doi: 10.1097/QAD.0b013e32833433df.
High levels of HIV-1 viremia exist in peripheral blood during acute and early infection; however, data on HIV-1 viral loads in female genital secretions during this period are sparse.
Prospective cohort of 188 African women with primary HIV-1 infection.
HIV-uninfected and infected women were followed quarterly; we tested serial plasma specimens by HIV PCR to estimate infection dates. We used the Loess procedure to estimate the magnitude and timing of viral setpoints in plasma and cervical secretions and generalized estimating equations (GEE) to identify predictors of plasma and cervical viral setpoints.
We estimated the mean HIV-1 plasma setpoint to be 4.20 log10 HIV-1 RNA copies/ml [95% confidence interval (CI) 4.04-4.35] at 121 days (95% CI 91-137) from infection; an analogous mean cervical viral setpoint was 1.64 log10 HIV-1 RNA copies/swab (95% CI 1.46-1.82) at 174 days (95% CI 145-194) from infection. Cervical loads were significantly higher (0.7-1.1 log10 copies/swab) during acute infection than subsequently. Subtype D infection, pregnancy, breastfeeding, and older age at the time of infection were associated with higher plasma viral setpoint. Subtype C infection, nonviral sexually transmitted infections, having a partner spending nights away from home, recent unprotected sex, and shorter time since infection were associated with higher cervical HIV-1 loads. Hormonal contraception was not associated with either the HIV-1 plasma setpoint or cervical loads during early infection.
Cervical HIV-1 viral loads were highest during acute infection and then declined up to 6 months following infection, when a 'setpoint' was attained. The prognostic value of a cervical 'setpoint' on future transmission risk remains unclear.
在急性和早期感染期间,外周血中存在高水平的 HIV-1 病毒血症;然而,在此期间女性生殖道中 HIV-1 病毒载量的数据很少。
188 名原发性 HIV-1 感染的非洲女性前瞻性队列研究。
未感染和感染 HIV 的女性每季度随访一次;我们通过 HIV PCR 检测连续的血浆标本,以估计感染日期。我们使用 Loess 程序估计血浆和宫颈分泌物中病毒基准的大小和时间,并使用广义估计方程(GEE)识别血浆和宫颈病毒基准的预测因素。
我们估计 HIV-1 血浆基准值的平均值为感染后 121 天(95%置信区间 91-137)时为 4.20 log10 HIV-1 RNA 拷贝/ml[95%置信区间(95%CI)4.04-4.35];类似的平均宫颈病毒基准值为感染后 174 天(95%CI 145-194)时为 1.64 log10 HIV-1 RNA 拷贝/拭子(95%CI 1.46-1.82)。在急性感染期间,宫颈负荷明显更高(0.7-1.1 log10 拷贝/拭子)。D 型感染、妊娠、母乳喂养和感染时年龄较大与较高的血浆病毒基准值相关。C 型感染、非病毒性性传播感染、伴侣离家过夜、最近无保护性行为和感染后时间较短与较高的宫颈 HIV-1 负荷相关。在早期感染期间,激素避孕与 HIV-1 血浆基准值或宫颈负荷无关。
在急性感染期间,宫颈 HIV-1 病毒载量最高,然后在感染后 6 个月下降,达到“基准值”。宫颈“基准值”对未来传播风险的预后价值尚不清楚。