Sun Yeqing, Huang Weijin, Xiang Hongyu, Nie Jianhui
School of Life Sciences, Jilin University, Changchun 130012, China.
Division of HIV/AIDS and Sex-Transmitted Virus Vaccines, National Institutes for Food and Drug Control, State Key Laboratory of Drug Regulatory Science, NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, NMPA Key Laboratory for Quality Research and Evaluation of Biological Products, Beijing 102629, China.
Vaccines (Basel). 2024 May 18;12(5):554. doi: 10.3390/vaccines12050554.
Since the emergence of COVID-19, extensive research efforts have been undertaken to accelerate the development of multiple types of vaccines to combat the pandemic. These include inactivated, recombinant subunit, viral vector, and nucleic acid vaccines. In the development of these diverse vaccines, appropriate methods to assess vaccine immunogenicity are essential in both preclinical and clinical studies. Among the biomarkers used in vaccine evaluation, the neutralizing antibody level serves as a pivotal indicator for assessing vaccine efficacy. Neutralizing antibody detection methods can mainly be classified into three types: the conventional virus neutralization test, pseudovirus neutralization test, and surrogate virus neutralization test. Importantly, standardization of these assays is critical for their application to yield results that are comparable across different laboratories. The development and use of international or regional standards would facilitate assay standardization and facilitate comparisons of the immune responses induced by different vaccines. In this comprehensive review, we discuss the principles, advantages, limitations, and application of different SARS-CoV-2 neutralization assays in vaccine clinical trials. This will provide guidance for the development and evaluation of COVID-19 vaccines.
自新冠病毒病出现以来,人们开展了广泛的研究工作,以加速多种类型疫苗的研发,以抗击这一疫情。这些疫苗包括灭活疫苗、重组亚单位疫苗、病毒载体疫苗和核酸疫苗。在研发这些不同类型的疫苗过程中,在临床前和临床研究中采用适当方法评估疫苗免疫原性至关重要。在用于疫苗评估的生物标志物中,中和抗体水平是评估疫苗效力的关键指标。中和抗体检测方法主要可分为三种类型:传统病毒中和试验、假病毒中和试验和替代病毒中和试验。重要的是,这些检测方法的标准化对于其应用至关重要,以便产生不同实验室之间可比的结果。国际或区域标准的制定和使用将有助于检测方法的标准化,并便于比较不同疫苗诱导的免疫反应。在这篇综述中,我们讨论了不同的严重急性呼吸综合征冠状病毒2中和试验在疫苗临床试验中的原理、优点、局限性及应用。这将为新冠病毒病疫苗的研发和评估提供指导。