Université Paris Descartes, Sorbonne Paris Cité, Faculté de Médecine, Paris, France; INSERM, U1016, CNRS, UMR8104, Institut Cochin, Paris, France; APHP, Laboratoire de Virologie, CHU Cochin, Paris, France.
Université Paris Descartes, Sorbonne Paris Cité, Faculté de Médecine, Paris, France; INSERM, U1016, CNRS, UMR8104, Institut Cochin, Paris, France.
J Virol Methods. 2021 Apr;290:114074. doi: 10.1016/j.jviromet.2021.114074. Epub 2021 Jan 22.
Recently, immunoblots (IBs) have tended to substitute Western blots (WBs) for HIV infection diagnosis. Several studies have confirmed IBs' high sensitivity to confirm HIV infection for every stage. Since the nature and pattern of the antigens of IBs are different from those of WB, the abilities of IBs and WBs to distinguish the stages of recent seroconversion and open-ended chronic infection might differ. We aimed to evaluate the performance of two IBs (INNO-LIA™ HIVI/II, Fujirebio, and Geenius™ HIV1/2 Confirmatory assay, Bio-Rad) to define the stage of infection. We studied 53 patients from the French ANRS CO6 PRIMO cohort. IBs have higher positive rates than WB. However, Geenius was less sensitive than WB and INNO-LIA to detect antibodies to p31 (0% vs 22.6 % and 15.1 %, respectively), so it could wrongly label late Fiebig stage and open-ended chronic infections as recent infections (n = 5/53). For the first time, we provide evidence that centralized WBs associated with an enzyme immunoassay for the identification of recent HIV-1 infection support the establishment of a more accurate diagnosis of primary HIV infection to improve the accuracy of enrollments in cohorts of recent HIV infections useful for epidemiological studies, pathogenesis studies or therapeutic trials.
最近,免疫印迹(IB)倾向于替代 Western blot(WB)用于 HIV 感染诊断。多项研究已经证实,IB 对每个阶段的 HIV 感染都具有很高的敏感性。由于 IB 与 WB 的抗原性质和模式不同,IB 和 WB 区分近期血清转化和开放性慢性感染阶段的能力可能存在差异。我们旨在评估两种免疫印迹(INNO-LIA™ HIVI/II,富士瑞比欧,和 Geenius™ HIV1/2 确认检测,伯乐)在确定感染阶段方面的性能。我们研究了来自法国 ANRS CO6 PRIMO 队列的 53 名患者。IB 的阳性率高于 WB。然而,与 WB 和 INNO-LIA 相比,Geenius 检测 p31 抗体的敏感性较低(分别为 0%、22.6%和 15.1%),因此可能错误地将晚期 Fiebig 期和开放性慢性感染标记为近期感染(n=5/53)。这是首次提供证据表明,集中的 WB 与酶免疫分析联合用于识别近期 HIV-1 感染,有助于更准确地诊断原发性 HIV 感染,从而提高在近期 HIV 感染队列中登记的准确性,这些队列对于流行病学研究、发病机制研究或治疗试验很有用。