Department of Research and Development, Sanofi Pasteur, Marcy L'Etoile, France.
Influenza Resource Centre, National Institute for Biological Standards and Control, Potters Bar, United Kingdom.
Front Immunol. 2022 Jun 17;13:909297. doi: 10.3389/fimmu.2022.909297. eCollection 2022.
Current vaccination strategies against influenza focus on generating an antibody response against the viral haemagglutination surface protein, however there is increasing interest in neuraminidase (NA) as a target for vaccine development. A critical tool for development of vaccines that target NA or include an NA component is available validated serology assays for quantifying anti-NA antibodies. Additionally serology assays have a critical role in defining correlates of protection in vaccine development and licensure. Standardisation of these assays is important for consistent and accurate results. In this study we first validated a harmonized enzyme-linked lectin assay (ELLA)- Neuraminidase Inhibition (NI) SOP for N1 influenza antigen and demonstrated the assay was precise, linear, specific and robust within classical acceptance criteria for neutralization assays for vaccine testing. Secondly we tested this SOP with NA from influenza B viruses and showed the assay performed consistently with both influenza A and B antigens. Third, we demonstrated that recombinant NA (rNA) could be used as a source of antigen in ELLA-NI. In addition to validating a harmonized SOP we finally demonstrated a clear improvement in inter-laboratory agreement across several studies by using a calibrator. Importantly we showed that the use of a calibrator significantly improved agreement when using different sources of antigen in ELLA-NI, namely reverse genetics viruses and recombinant NA. We provide a freely available and detailed harmonized SOP for ELLA-NI. Our results add to the growing body of evidence in support of developing biological standards for influenza serology.
目前针对流感的疫苗接种策略主要集中在产生针对病毒血凝素表面蛋白的抗体反应上,但人们对神经氨酸酶(NA)作为疫苗开发目标的兴趣越来越大。针对 NA 或包含 NA 成分的疫苗开发的关键工具是可用于定量抗 NA 抗体的经过验证的血清学检测。此外,血清学检测在疫苗开发和许可中确定保护相关性方面具有重要作用。这些检测的标准化对于获得一致和准确的结果非常重要。在这项研究中,我们首先验证了一种经过协调的酶联凝集素检测(ELLA)-神经氨酸酶抑制(NI)标准操作程序(SOP),用于 N1 流感抗原,并证明该检测在用于疫苗测试的中和检测的经典接受标准范围内具有精确性、线性、特异性和稳健性。其次,我们用流感 B 病毒的 NA 测试了该 SOP,并表明该检测与流感 A 和 B 抗原的性能一致。第三,我们证明了重组 NA(rNA)可以用作 ELLA-NI 中的抗原来源。除了验证一个协调的 SOP 外,我们还通过使用校准器,最终在几个研究中证明了实验室间协议的明显改善。重要的是,我们表明,在 ELLA-NI 中使用不同的抗原来源时,使用校准器可以显著提高一致性,即反向遗传学病毒和重组 NA。我们提供了一个免费的、详细的 ELLA-NI 协调 SOP。我们的结果为支持开发流感血清学的生物学标准提供了越来越多的证据。