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An Improved and High Throughput Respiratory Syncytial Virus (RSV) Micro-neutralization Assay
Published on: January 26, 2019
Challenges in developing a pediatric RSV vaccine
Jeanne H Schickli1, Filip Dubovsky, Roderick S Tang
1Research Department, MedImmune, Mountain View, CA, USA. schicklij@medimmune.com
Insights
Preventing respiratory syncytial virus (RSV) lower respiratory tract infection in infants is crucial. Live attenuated RSV vaccine candidates are promising, with two advanced into clinical studies for infant immunization.
Area of Science:
- Vaccinology
- Pediatric infectious diseases
- Virology
Background:
- Respiratory syncytial virus (RSV) bronchiolitis is a primary cause of infant hospitalization globally.
- A significant unmet need exists for effective RSV prevention strategies in young infants.
- Current RSV vaccine development faces challenges including maternal antibody interference and enhanced disease risk.
Purpose of the Study:
- To review the current landscape of RSV vaccine development for infants.
- To highlight the advantages of live attenuated RSV vaccine candidates.
- To introduce promising live attenuated RSV vaccine candidates progressing in clinical trials.
Main Methods:
- Review of existing vaccinology approaches for RSV prevention.
- Evaluation of live attenuated RSV vaccine candidates in preclinical models.
- Assessment of clinical trial progress for novel RSV vaccines.
Main Results:
- No RSV vaccine is currently approved for infant use.
- Live RSV infection elicits protective systemic and mucosal immunity without enhanced disease.
- Two live attenuated RSV vaccine candidates have advanced into clinical studies.
Conclusions:
- Live attenuated RSV vaccines are a preferred strategy due to their safety and immunogenicity profile.
- rA2cpts248/404/1030/DeltaSH and rb/h PIV3/RSV F2 represent promising candidates for infant RSV prevention.
- Further clinical evaluation is essential to establish the efficacy and safety of these live attenuated RSV vaccines.
Abstract:
RSV bronchiolitis is the leading cause of infant hospitalization in industrialized countries. There is an unmet need to prevent RSV lower respiratory tract infection in young infants. Although many vaccinology approaches, including live attenuated, viral and bacterial vectored and adjuvanted subunit vaccines have been evaluated in rodent and primate models there is currently no approved RSV vaccine. A vaccine candidate for RSV-naive infants must provide immunogenicity in the presence of maternally acquired antibodies, avoid enhanced disease and have minimal reactogenicity. Because live RSV infection does not potentiate for enhanced disease and elicits systemic and mucosal immune responses, live RSV vaccine candidates are currently preferred. Two live attenuated RSV vaccine candidates, rA2cpts248/404/1030/DeltaSH, a temperature sensitive RSV with a deletion of the SH gene, and rb/h PIV3/RSV F2 which has RSV F vectored into a bovine/human chimeric parainfluenza type 3 genome, have recently advanced into clinical studies.
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