Host Responses to Respiratory Syncytial Virus Infection

Viruses. 2023 Sep 26;15(10):1999. doi: 10.3390/v15101999.

Abstract

Respiratory syncytial virus (RSV) infections are a constant public health problem, especially in infants and older adults. Virtually all children will have been infected with RSV by the age of two, and reinfections are common throughout life. Since antigenic variation, which is frequently observed among other respiratory viruses such as SARS-CoV-2 or influenza viruses, can only be observed for RSV to a limited extent, reinfections may result from short-term or incomplete immunity. After decades of research, two RSV vaccines were approved to prevent lower respiratory tract infections in older adults. Recently, the FDA approved a vaccine for active vaccination of pregnant women to prevent severe RSV disease in infants during their first RSV season. This review focuses on the host response to RSV infections mediated by epithelial cells as the first physical barrier, followed by responses of the innate and adaptive immune systems. We address possible RSV-mediated immunomodulatory and pathogenic mechanisms during infections and discuss the current vaccine candidates and alternative treatment options.

Keywords: adaptive immunity; immune evasion; immunopathology; innate immunity; respiratory syncytial virus; vaccines.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Child
  • Female
  • Humans
  • Immunity
  • Infant
  • Pregnancy
  • Reinfection
  • Respiratory Syncytial Virus Infections*
  • Respiratory Syncytial Virus Vaccines*
  • Respiratory Syncytial Virus, Human*
  • Respiratory Syncytial Viruses
  • Vaccines*

Substances

  • Vaccines
  • Respiratory Syncytial Virus Vaccines

Grants and funding

This work was financially supported by the Innovative Medicines Initiative 2 of the European Union’s Horizon 2020 research and innovation program (EU IMI101007799, Inno4Vac) and the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—398066876/GRK 2485/2, Research Training Group VIPER. Open Access publication was funded by the DFG—491094227 “Open Access Publication Funding” and the University of Veterinary Medicine Hannover Foundation.