Harvard School of Public Health AIDS Initiative, Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts, United States of America.
PLoS One. 2010 Apr 12;5(4):e10148. doi: 10.1371/journal.pone.0010148.
The first aim of the study is to assess the distribution of HIV-1 RNA levels in subtype C infection. Among 4,348 drug-naïve HIV-positive individuals participating in clinical studies in Botswana, the median baseline plasma HIV-1 RNA levels differed between the general population cohorts (4.1-4.2 log(10)) and cART-initiating cohorts (5.1-5.3 log(10)) by about one log(10). The proportion of individuals with high (> or = 50,000 (4.7 log(10)) copies/ml) HIV-1 RNA levels ranged from 24%-28% in the general HIV-positive population cohorts to 65%-83% in cART-initiating cohorts. The second aim is to estimate the proportion of individuals who maintain high HIV-1 RNA levels for an extended time and the duration of this period. For this analysis, we estimate the proportion of individuals who could be identified by repeated 6- vs. 12-month-interval HIV testing, as well as the potential reduction of HIV transmission time that can be achieved by testing and ARV treating. Longitudinal analysis of 42 seroconverters revealed that 33% (95% CI: 20%-50%) of individuals maintain high HIV-1 RNA levels for at least 180 days post seroconversion (p/s) and the median duration of high viral load period was 350 (269; 428) days p/s. We found that it would be possible to identify all HIV-infected individuals with viral load > or = 50,000 (4.7 log(10)) copies/ml using repeated six-month-interval HIV testing. Assuming individuals with high viral load initiate cART after being identified, the period of high transmissibility due to high viral load can potentially be reduced by 77% (95% CI: 71%-82%). Therefore, if HIV-infected individuals maintaining high levels of plasma HIV-1 RNA for extended period of time contribute disproportionally to HIV transmission, a modified "test-and-treat" strategy targeting such individuals by repeated HIV testing (followed by initiation of cART) might be a useful public health strategy for mitigating the HIV epidemic in some communities.
本研究的首要目的是评估 HIV-1 RNA 水平在 C 型亚型感染中的分布。在博茨瓦纳参与临床研究的 4348 名未经药物治疗的 HIV 阳性个体中,普通人群队列(4.1-4.2log10)和开始 cART 队列(5.1-5.3log10)之间的中位基线血浆 HIV-1 RNA 水平相差约一个对数级。高(≥50000(4.7log10)拷贝/ml)HIV-1 RNA 水平个体的比例范围从普通 HIV 阳性人群队列的 24%-28%到开始 cART 队列的 65%-83%。第二个目的是估计维持较长时间高 HIV-1 RNA 水平的个体比例以及这段时间的持续时间。为此,我们通过重复的 6 个月和 12 个月的 HIV 检测,来估计可以识别的个体比例,以及通过检测和 ARV 治疗可能实现的 HIV 传播时间的潜在减少。42 例血清转换者的纵向分析显示,33%(95%置信区间:20%-50%)的个体在血清转换后至少 180 天(p/s)内维持高 HIV-1 RNA 水平,高病毒载量期的中位持续时间为 350(269;428)天 p/s。我们发现,使用重复的 6 个月间隔 HIV 检测,有可能识别所有病毒载量≥50000(4.7log10)拷贝/ml 的 HIV 感染个体。假设高病毒载量的个体在被识别后开始接受 cART,由于高病毒载量而导致的高传染性时期可能会减少 77%(95%置信区间:71%-82%)。因此,如果维持高水平血浆 HIV-1 RNA 时间较长的 HIV 感染者对 HIV 传播的贡献不成比例,那么通过重复 HIV 检测(随后开始 cART)针对这些个体的“检测和治疗”策略的修改可能是减轻某些社区 HIV 流行的一种有用的公共卫生策略。