Value profile for respiratory syncytial virus vaccines and monoclonal antibodies

Jessica A Fleming1, Ranju Baral1, Deborah Higgins1

  • 1Center for Vaccine Innovation and Access, PATH, 2201 Westlake Ave Suite 200, Seattle, WA 98121, United States.

Vaccine
|July 8, 2023
PubMed

Insights

No licensed respiratory syncytial virus (RSV) vaccine exists for children, but maternal vaccines and infant monoclonal antibodies (mAbs) show promise for prevention. These interventions are likely cost-effective and feasible within 1-3 years.

Area of Science:

  • * Public Health and Vaccinology
  • * Infectious Disease Prevention
  • * Pediatric Health

Background:

  • * Respiratory syncytial virus (RSV) is a leading cause of acute lower respiratory infection (ALRI) in young children globally.
  • * Current prevention options, like monoclonal antibody (mAb) prophylaxis, are limited, costly, and impractical for widespread use, especially in low-income settings.
  • * There is a critical unmet need for effective and accessible RSV prevention strategies for infants and children.

Purpose of the Study:

  • * To assess the potential public health, economic, and societal value of emerging RSV vaccines and vaccine-like products.
  • * To identify current research and knowledge gaps concerning RSV prevention strategies.
  • * To inform the development and implementation of future RSV interventions.

Main Methods:

  • * Development of a Vaccine Value Profile (VVP) for RSV.
  • * Holistic assessment of available data on pipeline RSV vaccines and passive immunization approaches.
  • * Expert working group collaboration with stakeholders from academia, non-profit organizations, public-private partnerships, multi-lateral organizations, and WHO.

Main Results:

  • * Two promising passive immunization approaches for low-income contexts: maternal RSV vaccines and long-acting infant mAbs.
  • * Feasible licensure of one or more candidates within one to three years.
  • * Economic models suggest both maternal vaccines and infant mAbs are likely to be cost-effective.

Conclusions:

  • * Maternal RSV vaccines and infant mAbs represent viable strategies for preventing RSV disease in pediatric populations.
  • * Effective, efficient, and equitable delivery will require strong coordination between maternal/child health programs and immunization initiatives.
  • * Further research and data are needed to address knowledge gaps and optimize the value of these emerging interventions.

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