Ndlovu Kwazi C Z, Sibanda Wilbert, Assounga Alain
Inkosi Albert Luthuli Central Hospital, Durban, South Africa.
Department of Nephrology, University of KwaZulu-Natal, Durban, South Africa.
Nephrol Dial Transplant. 2017 Apr 1;32(4):714-721. doi: 10.1093/ndt/gfx001.
We evaluated the shedding of human immunodeficiency virus (HIV)-1 particles into continuous ambulatory peritoneal dialysis (CAPD) effluents of HIV-positive patients with end-stage renal disease (ESRD).
A total of 58 HIV-positive patients with ESRD on highly active antiretroviral therapy (HAART) who had Tenckhoff catheters inserted between September 2012 and February 2015 were prospectively reviewed and followed for 18 months. Peritoneal dialysis (PD) effluent samples from functioning CAPD catheters and plasma samples were obtained at three points during regular clinic visits on days 45 ± 37, 200 ± 19 and 377 ± 13 after catheter insertion. All specimens were stored at -20°C, and each batch was analysed by Roche quantitative HIV-1 polymerase chain reaction assay to detect HIV-1 particles. Clustered logistic regression was used to test for independent predictors of HIV-1 detection in CAPD effluents.
HIV-1 RNA above 20 copies/mL assay limit was detectable in 19% (first batch), 26.3% (second batch) and 20% (third batch) of PD effluent specimens. HIV-1 RNA was detectable in PD fluid, without corresponding detection in the paired plasma in 3.4% (first batch), 5.3% (second batch) and 10% (third batch) of samples. Detection of HIV-1 in plasma sample (odds ratios 3.94; 95% confidence interval 1.14-13.55; P = 0.030), body mass index, serum albumin and HAART regimen were found to be significantly associated with HIV-1 detection in PD effluents.
HIV particles are shed in detectable amounts into CAPD effluents even in patients with suppressed plasma viral load, raising concerns of a localized sanctuary site and potential infectivity of HIV-positive CAPD patients on a full complement of HAART.
我们评估了终末期肾病(ESRD)的HIV阳性患者在持续性非卧床腹膜透析(CAPD)流出液中人类免疫缺陷病毒(HIV)-1颗粒的释放情况。
对2012年9月至2015年2月期间插入Tenckhoff导管的58例接受高效抗逆转录病毒治疗(HAART)的ESRD HIV阳性患者进行前瞻性回顾,并随访18个月。在导管插入后第45±37天、200±19天和377±13天的定期门诊就诊期间的三个时间点,采集来自功能正常的CAPD导管的腹膜透析(PD)流出液样本和血浆样本。所有标本均储存在-20°C,每一批次均通过罗氏定量HIV-1聚合酶链反应测定法进行分析以检测HIV-1颗粒。采用聚类逻辑回归分析来检测CAPD流出液中HIV-1检测的独立预测因素。
在19%(第一批)、26.3%(第二批)和20%(第三批)的PD流出液标本中可检测到高于20拷贝/mL检测限的HIV-1 RNA。在3.4%(第一批)、5.3%(第二批)和10%(第三批)的样本中,PD液中可检测到HIV-1 RNA,而配对血浆中未检测到相应病毒。血浆样本中HIV-1的检测(比值比3.94;95%置信区间1.14-13.55;P = 0.030)、体重指数、血清白蛋白和HAART方案被发现与PD流出液中HIV-1的检测显著相关。
即使血浆病毒载量得到抑制,HIV颗粒仍会以可检测的量释放到CAPD流出液中,这引发了对局部庇护所部位以及接受完整HAART方案的HIV阳性CAPD患者潜在传染性的担忧。