Tinguely Caroline, Schild-Spycher Therese, Bahador Zahra, Gowland Peter, Stolz Martin, Niederhauser Christoph
Blood Transfusion Service SRC Berne, Murtenstrasse 133, 3008 Berne, Switzerland.
Blood Transfusion Service SRC Berne, Murtenstrasse 133, 3008 Berne, Switzerland.
J Virol Methods. 2014 Sep;206:1-4. doi: 10.1016/j.jviromet.2014.05.010. Epub 2014 May 27.
The performance of the rapid confirmatory HIV 1/2 assay Geenius was compared with the conventional HIV 1/2 line immunoblot (INNO-LIA HIV I/II Score). One hundred HIV 1/2 confirmed positive samples from donors and patients and 136 negative screening samples from blood donors were evaluated with both assays. A 20 member performance panel consisting of different HIV 1 and 2 subtypes was also analysed. Ninety-nine of the confirmed HIV positive samples were positive with both assays. One sample was positive with the INNO-LIA HIV I/II Score but indeterminate with the Geenius HIV 1/2. From 136 negative blood donor samples (negative with a combo HIV assay and a highly sensitive ID-NAT), 125 were concordant negative. Six and five samples were incorrectly indeterminate with the INNO-LIA HIV I/II Score and the Geenius HIV 1/2, respectively. One sample was weak positive with the INNO-LIA HIV I/II Score but negative with the Geenius HIV 1/2. The 20 member performance showed equivalent results with both assays. The rapid assay showed a comparable sensitivity and specificity for confirmation for positive and negative HIV donor and patient samples as well for a 20 member performance panel.
将快速确证性HIV 1/2检测试剂Geenius与传统的HIV 1/2线性免疫印迹法(INNO-LIA HIV I/II Score)进行了比较。使用这两种检测方法对来自献血者和患者的100份HIV 1/2确证阳性样本以及来自献血者的136份阴性筛查样本进行了评估。还分析了一个由不同HIV 1和2亚型组成的20份样本的性能评估组。99份确证的HIV阳性样本在两种检测方法中均呈阳性。1份样本在INNO-LIA HIV I/II Score检测中呈阳性,但在Geenius HIV 1/2检测中结果不确定。在136份阴性献血者样本(联合HIV检测和高灵敏度ID-NAT检测均为阴性)中,125份结果一致为阴性。分别有6份和5份样本在INNO-LIA HIV I/II Score检测和Geenius HIV 1/2检测中被错误地判定为不确定。1份样本在INNO-LIA HIV I/II Score检测中呈弱阳性,但在Geenius HIV 1/2检测中为阴性。这个由20份样本组成的性能评估组在两种检测方法中显示出等效的结果。对于HIV阳性和阴性的献血者及患者样本以及一个由20份样本组成的性能评估组,这种快速检测方法在确证方面显示出相当的灵敏度和特异性。