Establishment and validation of a high-throughput micro-neutralization assay for respiratory syncytial virus (subtypes A and B)

J Med Virol. 2023 Jul;95(7):e28923. doi: 10.1002/jmv.28923.

Abstract

The validation of a bioanalytical method allows us to determine its validity for a designated purpose and to guarantee the reliability of its analytical results. The virus neutralization assay has proved to be suitable for the detection and quantification of specific serum-neutralizing antibodies against respiratory syncytial virus subtypes A and B. Respiratory syncytial virus is a negative-sense RNA virus and is responsible for the majority of acute lower respiratory tract infections in infants and older adults worldwide. Owing to its widespread infection, the WHO considers it a target for the development of preventive vaccines. Despite the high impact of its infections, however, only one vaccine has been recently approved. The aim of this paper is to provide a detailed validation process for the microneutralization assay and to demonstrate that this method can effectively support the efficacy assessment of candidate vaccines and the definition of correlates of protection.

Keywords: correlates of protection; neutralization; respiratory syncytial virus; validation.

MeSH terms

  • Aged
  • Antibodies, Neutralizing
  • Antibodies, Viral
  • Humans
  • Infant
  • Reproducibility of Results
  • Respiratory Syncytial Virus Infections* / diagnosis
  • Respiratory Syncytial Virus Infections* / prevention & control
  • Respiratory Syncytial Virus, Human* / genetics

Substances

  • Antibodies, Viral
  • Antibodies, Neutralizing