HIV Reference Laboratory, Virology Laboratory, Department of Microbiology, Division of Pathology, Singapore General Hospital, Singapore, Singapore.
Duke-NUS Medical School, Singapore, Singapore.
PLoS One. 2018 Jun 21;13(6):e0199502. doi: 10.1371/journal.pone.0199502. eCollection 2018.
In view of recent revised recommendations for human immunodeficiency virus (HIV) confirmatory testing, the performance of 3 HIV confirmatory assays was compared. Using the HIV Blot 2.2 (MP-WB), the INNO-LIA HIV I/II Score (INNO), and the Geenius HIV 1/2 Confirmatory Assay (Geenius), we tested 199 HIV-1 positive, 161 HIV negative, 65 HIV western blot indeterminate, 26 HIV seroconversion, 34 early HIV infection and 4 HIV-2 positive archived specimens. We show that all 3 assays had comparable test sensitivity in the detection of HIV-1 positive cases. However, less non-specific reactivity was observed with the INNO and Geenius assays, where both of them were able to resolve MP-WB indeterminate cases. When early HIV cases were considered, INNO and Geenius were more likely to confirm an early-stage infection as positive. Nevertheless, overall poor sensitivity (25.5% - 44.7%) of these assays for the detection of early cases was observed, likely because these cases had very low or non-detectable levels of HIV antibodies. Hence, further testing by a nucleic acid test or a p24 antigen test of specimens reactive on screening with a fourth generation Ag/Ab assay that are negative on confirmatory testing for HIV-specific antibody, may be useful. In conclusion, INNO and Geenius had comparable test performance, although the ease of use and shorter assay time for Geenius may make it the preferred choice for laboratories. In that regard, of note is our observation of non-specific reactivity of lipaemic specimens to the HIV-2 gp140 band in the Geenius assay, which should prompt caution when interpreting results of such specimens.
鉴于最近对人类免疫缺陷病毒 (HIV) 确认检测的修订建议,比较了 3 种 HIV 确认检测方法的性能。我们使用 HIV Blot 2.2 (MP-WB)、INNO-LIA HIV I/II Score (INNO) 和 Geenius HIV 1/2 确认检测试剂盒 (Geenius) ,检测了 199 份 HIV-1 阳性、161 份 HIV 阴性、65 份 HIV 免疫印迹不确定、26 份 HIV 血清转换、34 份早期 HIV 感染和 4 份 HIV-2 阳性的存档标本。结果显示,所有 3 种检测方法在检测 HIV-1 阳性病例时均具有相当的检测灵敏度。然而,与 INNO 和 Geenius 检测方法相比,观察到较少的非特异性反应,这两种方法都能够解决 MP-WB 不确定病例的问题。当考虑早期 HIV 病例时,INNO 和 Geenius 更有可能确认早期感染呈阳性。然而,这些检测方法对早期病例的总体检测灵敏度(25.5%至 44.7%)较差,这可能是因为这些病例的 HIV 抗体水平非常低或无法检测到。因此,对于通过第四代 Ag/Ab 检测呈反应性且 HIV 特异性抗体确认检测为阴性的标本,进一步进行核酸检测或 p24 抗原检测可能是有用的。总之,INNO 和 Geenius 的检测性能相当,尽管 Geenius 的易用性和较短的检测时间可能使其成为实验室的首选。在这方面,值得注意的是我们观察到 Geenius 检测中脂血标本对 HIV-2 gp140 带的非特异性反应,这在解释此类标本的结果时应引起警惕。