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Updated: Jul 24, 2025

An Improved and High Throughput Respiratory Syncytial Virus RSV Micro-neutralization Assay
Published on: January 26, 2019
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.
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.
Abstract:
Respiratory syncytial virus (RSV) is the predominant cause of acute lower respiratory infection (ALRI) in young children worldwide, yet no licensed RSV vaccine exists to help prevent the millions of illnesses and hospitalizations and tens of thousands of young lives taken each year. Monoclonal antibody (mAb) prophylaxis exists for prevention of RSV in a small subset of very high-risk infants and young children, but the only currently licensed product is impractical, requiring multiple doses and expensive for the low-income settings where the RSV disease burden is greatest. A robust candidate pipeline exists to one day prevent RSV disease in infant and pediatric populations, and it focuses on two promising passive immunization approaches appropriate for low-income contexts: maternal RSV vaccines and long-acting infant mAbs. Licensure of one or more candidates is feasible over the next one to three years and, depending on final product characteristics, current economic models suggest both approaches are likely to be cost-effective. Strong coordination between maternal and child health programs and the Expanded Program on Immunization will be needed for effective, efficient, and equitable delivery of either intervention. This 'Vaccine Value Profile' (VVP) for RSV is intended to provide a high-level, holistic assessment of the information and data that are currently available to inform the potential public health, economic and societal value of pipeline vaccines and vaccine-like products. This VVP was developed by a working group of subject matter experts from academia, non-profit organizations, public private partnerships and multi-lateral organizations, and in collaboration with stakeholders from the WHO headquarters. All contributors have extensive expertise on various elements of the RSV VVP and collectively aimed to identify current research and knowledge gaps. The VVP was developed using only existing and publicly available information.
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