Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, United States of America.
PLoS One. 2014 Mar 6;9(3):e86461. doi: 10.1371/journal.pone.0086461. eCollection 2014.
BACKGROUND: Dried blood spots (DBS) have been used as alternative specimens to plasma to increase access to HIV viral load (VL) monitoring and early infant diagnosis (EID) in remote settings. We systematically reviewed evidence on the performance of DBS compared to plasma for VL monitoring and EID. METHODS AND FINDINGS: Thirteen peer reviewed HIV VL publications and five HIV EID papers were included. Depending on the technology and the viral load distribution in the study population, the percentage of DBS samples that are within 0.5 log of VL in plasma ranged from 52-100%. Because the input sample volume is much smaller in a blood spot, there is a risk of false negatives with DBS. Sensitivity of DBS VL was found to be 78-100% compared to plasma at VL below 1000 copies/ml, but this increased to 100% at a threshold of 5000 copies/ml. Unlike a plasma VL test which measures only cell free HIV RNA, a DBS VL also measures proviral DNA as well as cell-associated RNA, potentially leading to false positive results when using DBS. The systematic review showed that specificity was close to 100% at DBS VL above 5000 copies/ml, and this threshold would be the most reliable for predicting true virologic failure using DBS. For early infant diagnosis, DBS has a sensitivity of 100% compared to fresh whole blood or plasma in all studies. CONCLUSIONS: Although limited data are available for EID, DBS offer a highly sensitive and specific sampling strategy to make viral load monitoring and early infant diagnosis more accessible in remote settings. A standardized approach for sampling, storing, and processing DBS samples would be essential to allow successful implementation. TRIAL REGISTRATION: PROSPERO Registration #: CRD42013003621.
背景:干血斑(DBS)已被用作替代血浆的标本,以增加在偏远地区进行 HIV 病毒载量(VL)监测和早期婴儿诊断(EID)的机会。我们系统地回顾了 DBS 与血浆进行 VL 监测和 EID 的比较的证据。
方法和发现:纳入了 13 篇同行评议的 HIV VL 出版物和 5 篇 HIV EID 论文。根据技术和研究人群中病毒载量的分布,DBS 样本与血浆中 VL 相差 0.5 对数的百分比范围为 52-100%。由于在血斑中输入的样本量要小得多,因此 DBS 存在假阴性的风险。与 VL 低于 1000 拷贝/ml 的血浆相比,DBS VL 的灵敏度为 78-100%,但在阈值为 5000 拷贝/ml 时增加到 100%。与仅测量无细胞 HIV RNA 的血浆 VL 测试不同,DBS VL 还测量前病毒 DNA 以及细胞相关 RNA,当使用 DBS 时,这可能导致假阳性结果。系统评价表明,当 DBS VL 高于 5000 拷贝/ml 时,特异性接近 100%,并且该阈值将是使用 DBS 预测真正病毒学失败的最可靠方法。对于早期婴儿诊断,在所有研究中,DBS 与新鲜全血或血浆相比,具有 100%的灵敏度。
结论:尽管 EID 的数据有限,但 DBS 提供了一种高度敏感和特异的采样策略,可以使病毒载量监测和早期婴儿诊断在偏远地区更容易实现。采样、储存和处理 DBS 样本的标准化方法对于成功实施至关重要。
试验注册:PROSPERO 注册编号:CRD42013003621。
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