Vismederi, Siena, Italy, 53100, Italy.
Life-Science, University of Siena, Siena, Italy.
F1000Res. 2024 Oct 14;13:534. doi: 10.12688/f1000research.149578.2. eCollection 2024.
Over the past few decades, World Health Organization (WHO) has made massive efforts to promote the development of a vaccine against Lassa virus (LASV), one of the top ten priority pathogens for research and development under the WHO R&D Blueprint for Emerging Infections. To date, several vaccines are at different stages of development. In this scenario, a validated and standardised assay to measure LASV neutralising antibodies is urgently needed for vaccine development and comparison.
The neutralisation assay remains the gold standard for determining antibody efficacy. Here we have proposed a safe and validated pseudotyped neutralisation assay for LASV, taking advantage of the development of the first WHO International Standard and Reference Panel for Anti-Lassa Fever (NIBSC code 21/332).
The proposed results demonstrate that the pseudotyped luciferase neutralisation assay is a specific serological test for the measurement of LASV neutralising antibodies without cross-reacting with standard sera specific for heterologous viral infections. In addition, the assay is accurate, precise, and linear according to criteria and statistical analyses defined and accepted by international guidelines.
在过去几十年中,世界卫生组织(WHO)为推动拉沙病毒(LASV)疫苗的发展做出了巨大努力,LASV 是世卫组织研发新兴传染病蓝图中十大优先病原体研究和开发之一。迄今为止,有几种疫苗处于不同的开发阶段。在这种情况下,迫切需要一种经过验证和标准化的测定 LASV 中和抗体的检测方法,以用于疫苗开发和比较。
中和测定仍然是确定抗体疗效的金标准。在这里,我们利用首个世界卫生组织拉沙热国际标准和参考品(NIBSC 编号 21/332)的开发,提出了一种用于 LASV 的安全且经过验证的假型中和测定方法。
提出的结果表明,假型荧光素酶中和测定是一种用于测量 LASV 中和抗体的特异性血清学检测方法,与针对异源病毒感染的标准血清无交叉反应。此外,根据国际指南定义和接受的标准和统计分析,该测定方法准确、精密且呈线性。