通过野生型噬斑减少中和试验、微量中和试验和假型病毒中和试验来定量 SARS-CoV-2 中和抗体。
Quantification of SARS-CoV-2 neutralizing antibody by wild-type plaque reduction neutralization, microneutralization and pseudotyped virus neutralization assays.
机构信息
National Infection Service, Public Health England, Salisbury, UK.
Nexelis, Laval, Quebec, Canada.
出版信息
Nat Protoc. 2021 Jun;16(6):3114-3140. doi: 10.1038/s41596-021-00536-y. Epub 2021 Apr 23.
Virus neutralization assays measure neutralizing antibodies in serum and plasma, and the plaque reduction neutralization test (PRNT) is considered the gold standard for measuring levels of these antibodies for many viral diseases. We have developed procedures for the standard PRNT, microneutralization assay (MNA) and pseudotyped virus neutralization assay (PNA) for severe acute respiratory syndrome coronavirus 2. The MNA offers advantages over the PRNT by reducing assay time, allowing increased throughput and reducing operator workload while remaining dependent upon the use of wild-type virus. This ensures that all severe acute respiratory syndrome coronavirus 2 antigens are present, but Biosafety Level 3 facilities are required. In addition to the advantages of MNA, PNA can be performed with lower biocontainment (Biosafety Level 2 facilities) and allows for further increases in throughput. For each new vaccine, it is critical to ensure good correlation of the neutralizing activity measured using PNA against the PRNT or MNA. These assays have been used in the development and licensure of the ChAdOx1 nCoV-19 (AstraZeneca; Oxford University) and Ad26.COV2.S (Janssen) coronavirus disease 2019 vaccines and are critical for demonstrating bioequivalence of future vaccines.
病毒中和测定法用于测量血清和血浆中的中和抗体,而蚀斑减少中和试验(PRNT)被认为是许多病毒疾病中测量这些抗体水平的金标准。我们已经为严重急性呼吸综合征冠状病毒 2 开发了标准 PRNT、微量中和测定法(MNA)和假型病毒中和测定法(PNA)的程序。MNA 通过减少测定时间、增加通量并减少操作人员的工作量,同时仍然依赖于使用野生型病毒,从而优于 PRNT。这确保了所有严重急性呼吸综合征冠状病毒 2 抗原都存在,但需要生物安全 3 级设施。除了 MNA 的优势外,PNA 可以在较低的生物安全 2 级设施下进行,并且可以进一步增加通量。对于每种新疫苗,至关重要的是要确保使用 PNA 测量的中和活性与 PRNT 或 MNA 之间具有良好的相关性。这些测定法已用于 ChAdOx1 nCoV-19(阿斯利康;牛津大学)和 Ad26.COV2.S(杨森)冠状病毒病 2019 疫苗的开发和许可,对于证明未来疫苗的生物等效性至关重要。