Kiely P, Styles C
Australian Red Cross Blood Service, Melbourne, Vic., Australia.
Australian Red Cross Blood Service, Perth, WA, Australia.
Vox Sang. 2017 Aug;112(6):542-548. doi: 10.1111/vox.12547.
The significance of anti-HCV immunoblot (IB) indeterminate results can be difficult to determine. We analysed results for blood donors tested on the MP Diagnostics HCV Blot 3.0 IB assay to determine whether indeterminate results representing past exposure to HCV could be distinguished from those due to non-specific reactivity.
Results for all donors tested by IB during the study period (July 2010 to December 2013) were included in this study.
Of 131 donors tested by IB, 34 (26.0%) were negative, 38 (29.0%) were indeterminate, and 59 (45.0%) were positive. There was no significant difference in IB band reactivity strength between indeterminate and positive donors. The PRISM HCV chemiluminescent immunoassay (ChLIA) sample to cut-off (s/co) ratio distribution for the indeterminate donors was significantly higher than for those with biological false reactivity (P = 0·037), but significantly lower than for donors who were IB positive/HCV RNA negative (P < 0·001) or IB not tested/HCV RNA positive (P < 0·001). Of donors available for follow-up, 53.1% of the indeterminate group disclosed a putative risk factor for HCV infection compared to 39.4% (P < 0·001) for the IB-negative group, 76.6% (P = 0·065) for the IB-positive group and 83.4% (P < 0·001) for the HCV RNA-positive group.
The results of this study indicate that PRISM ChLIA s/co ratios >2·00 with IB indeterminate results predict exposure to HCV, particularly in the presence of putative risk factors for HCV infection. These findings may be applied to optimizing counselling of donors with indeterminate HCV results.
抗丙型肝炎病毒免疫印迹法(IB)检测结果不确定时其意义难以判定。我们分析了在MP诊断公司丙型肝炎病毒印迹3.0免疫印迹检测中接受检测的献血者的结果,以确定代表既往丙型肝炎病毒暴露的不确定结果是否能与非特异性反应导致的结果区分开来。
本研究纳入了研究期间(2010年7月至2013年12月)所有通过免疫印迹法检测的献血者的结果。
在131名接受免疫印迹法检测的献血者中,34名(26.0%)为阴性,38名(29.0%)结果不确定,59名(45.0%)为阳性。结果不确定的献血者与阳性献血者之间免疫印迹条带反应强度无显著差异。结果不确定的献血者的PRISM丙型肝炎病毒化学发光免疫分析(ChLIA)样本与临界值(s/co)比值分布显著高于具有生物学假反应性的献血者(P = 0.037),但显著低于免疫印迹阳性/丙型肝炎病毒RNA阴性的献血者(P < 0.001)或免疫印迹未检测/丙型肝炎病毒RNA阳性的献血者(P < 0.001)。在可供随访的献血者中,结果不确定组有53.1%披露了丙型肝炎病毒感染的假定危险因素,相比之下,免疫印迹阴性组为39.4%(P < 0.001),免疫印迹阳性组为76.6%(P = 0.065),丙型肝炎病毒RNA阳性组为83.4%(P < 0.001)。
本研究结果表明,PRISM ChLIA s/co比值>2.00且免疫印迹结果不确定预示着丙型肝炎病毒暴露,尤其是在存在丙型肝炎病毒感染假定危险因素的情况下。这些发现可应用于优化对丙型肝炎病毒检测结果不确定的献血者的咨询。