Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
School of Information and Computing, Pittsburgh, PA, USA.
Am J Clin Pathol. 2022 Aug 4;158(2):162-166. doi: 10.1093/ajcp/aqac025.
Acute viral infections and some vaccines have been shown to increase false positivity in serologic assays. We assessed if the messenger RNA coronavirus disease 2019 (COVID-19) vaccines could cause false reactivity in common serologic assays in a pilot longitudinal cohort.
Thirty-eight participants with sera available prevaccination, 2 weeks after each vaccine dose, and monthly thereafter for up to 5 months were tested for common infectious disease serologies and antiphospholipid syndrome (APS) serology markers on the BioPlex 2200, Sure-Vue rapid plasma reagin (RPR), and Macro-Vue RPR. Twenty-two participants received the Moderna vaccine and 16 received the Pfizer vaccine.
Most assays had no change in reactivity over the course of the sample draws, including APS markers. Epstein-Barr virus immunoglobulin G (IgG), measles IgG, and rubella immunoglobulin M all had possible false reactivity in one to two participants. RPR tests demonstrated false reactivity, with baseline nonreactive participant samples becoming reactive following vaccination. There were more false reactive participants (7/38) in the BioPlex RPR than in the Sure-Vue (2/38) and Macro-Vue (1/38) tests. All falsely reactive RPR tests were in participants who received the Moderna vaccine.
Serologic assays with results that do not fit the clinical picture following COVID-19 vaccination should be repeated. Effects of false reactivity can last more than 5 months in some assays. In particular, RPR is susceptible to false reactivity, and there is variability among assays. Larger longitudinal studies are needed to determine the incidence and window of false reactivity.
急性病毒感染和某些疫苗已被证明会增加血清学检测的假阳性率。我们评估了信使 RNA 新型冠状病毒病 2019(COVID-19)疫苗是否会在一个试点纵向队列中引起常见血清学检测的假反应。
38 名参与者在接种疫苗前、每次接种疫苗后 2 周以及此后每月均有血清样本可供检测,最多可检测 5 个月,检测项目包括常见传染病血清学和抗磷脂综合征(APS)血清学标志物,检测方法为 BioPlex 2200、Sure-Vue 快速血浆反应素(RPR)和 Macro-Vue RPR。22 名参与者接受了 Moderna 疫苗,16 名参与者接受了 Pfizer 疫苗。
在样本采集过程中,大多数检测的反应性没有变化,包括 APS 标志物。在 1 到 2 名参与者中,EB 病毒免疫球蛋白 G(IgG)、麻疹 IgG 和风疹免疫球蛋白 M 均可能出现假阳性反应。RPR 检测显示出假阳性反应,基线时无反应的参与者样本在接种疫苗后变得有反应。在 BioPlex RPR 中,有更多的假阳性反应参与者(7/38),而在 Sure-Vue(2/38)和 Macro-Vue(1/38)中,假阳性反应参与者较少。所有假阳性的 RPR 检测均来自接受 Moderna 疫苗的参与者。
COVID-19 疫苗接种后结果与临床情况不符的血清学检测应重复进行。在某些检测中,假阳性反应的影响可持续超过 5 个月。特别是 RPR 容易出现假阳性反应,并且不同检测之间存在差异。需要进行更大规模的纵向研究,以确定假阳性反应的发生率和窗口期。