Assessment of twelve echovirus virus-neutralisation assays in Europe: recommendations for harmonisation of non-polio enterovirus sero-surveillance studies.

IF 3.6 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of General Virology Pub Date : 2024-09-01 DOI:10.1099/jgv.0.001986
Karen Couderé, Kimberley S M Benschop, Gerrit Koen, Hetty van Eijk, Heli Harvala, Jean-Luc Bailly, Maël Bessaud, Everlyn Kamau, Isabelle Simon, Marie-Line Joffret, Lubomira Nikolaeva-Glomb, Irina Georgieva, Asya Stoyanova, Sabine Diedrich, Sindy Böttcher, Maria Cabrerizo, Irena Tabain, Željka Hruškar, Vladimir Stevanović, Petri Susi, Eero Hietanen, Paula Palminha, Petra Rainetová, Anda Baicus, Maartje Kristensen, Dasja Pajkrt, Jean-Luc Murk, Katja C Wolthers, European Non-Polio Enterovirus Network
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Abstract

Non-polio enteroviruses (NPEV) cause significant disease worldwide. Population-based sero-surveillance, by measuring antibodies against specific NPEV types, provides additional information on past circulation and the prediction for future upsurges. Virus neutralisation assays (VNA), the current method of choice for measuring NPEV type specific antibodies, are not entirely standardised. Via the European Non-Polio Enterovirus Network, we organised a VNA quality assessment in which twelve laboratories participated. We provided five echovirus (E) types (E1, E18, E30 G2, E30 G6 and E6) and intravenous immunoglobulins (IVIG) as a sample for the NPEV VNA quality assessment. Differences in VNA protocols and neutralising Ab (nAb) titres were found between the participating laboratories with geometric coefficients of variation ranging from 10.3-62.9 %. Mixed-effects regression analysis indicated a small but significant effect of type of cell line used. Harmonisation of cell line passage number, however, did not improve variation between laboratories. Calibration by making use of a reference sample, reduced variation between laboratories but differences in nAb titres remained higher than two log2 dilution steps. In conclusion, sero-surveillance data from different laboratories should be compared with caution and standardised protocols are needed.

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欧洲十二种埃可病毒中和检测方法评估:关于统一非脊髓灰质炎肠道病毒血清监测研究的建议。
非脊髓灰质炎肠道病毒(NPEV)在全球范围内引发大量疾病。通过测量特定 NPEV 类型的抗体来进行基于人群的血清监测,可提供有关过去传播情况的更多信息,并预测未来的疫情激增。病毒中和检测法(VNA)是目前测量非脊髓灰质炎病毒特定类型抗体的首选方法,但尚未完全标准化。我们通过欧洲非脊髓灰质炎肠道病毒网络(European Non-Polio Enterovirus Network)组织了一次 VNA 质量评估,共有 12 家实验室参加。我们提供了五种埃可病毒 (E) 类型(E1、E18、E30 G2、E30 G6 和 E6)和静脉注射免疫球蛋白 (IVIG) 作为 NPEV VNA 质量评估的样本。参与评估的实验室在 VNA 方案和中和抗体 (nAb) 滴度方面存在差异,几何变异系数在 10.3%-62.9% 之间。混合效应回归分析表明,所使用的细胞系类型会产生微小但显著的影响。然而,统一细胞系通过数并不能改善实验室之间的差异。使用参考样本进行校准可减少实验室之间的差异,但 nAb 滴度的差异仍高于两个 log2 稀释级。总之,应谨慎比较不同实验室的血清监测数据,并需要制定标准化方案。
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来源期刊
Journal of General Virology
Journal of General Virology 医学-病毒学
CiteScore
7.70
自引率
2.60%
发文量
91
审稿时长
3 months
期刊介绍: JOURNAL OF GENERAL VIROLOGY (JGV), a journal of the Society for General Microbiology (SGM), publishes high-calibre research papers with high production standards, giving the journal a worldwide reputation for excellence and attracting an eminent audience.
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