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Updated: May 30, 2026

Influenza A Virus Studies in a Mouse Model of Infection
Published on: September 7, 2017
Progress in the development of human parainfluenza virus vaccines
Alexander C Schmidt1, Anne Schaap-Nutt, Emmalene J Bartlett
1RNA Viruses Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. schmidta@niaid.nih.gov
Insights
Human parainfluenza viruses (HPIVs) cause significant childhood respiratory illness. Live-attenuated intranasal vaccines for HPIV3 show promise in early trials, with HPIV1 and HPIV2 vaccines in development.
Area of Science:
- Virology
- Vaccinology
- Pediatric infectious diseases
Background:
- Human parainfluenza viruses (HPIVs) are a leading cause of pediatric acute respiratory illness requiring hospitalization.
- HPIVs rank second only to respiratory syncytial virus in this regard, preceding influenza viruses.
Purpose of the Study:
- To evaluate the safety, tolerability, and immunogenicity of novel live-attenuated intranasal vaccines against HPIV serotypes 1, 2, and 3.
- To advance vaccine candidates for HPIV3 into proof-of-concept trials based on promising Phase I data.
Main Methods:
- Development of live-attenuated HPIV vaccines using reverse genetics systems for HPIV1, HPIV2, and HPIV3.
- Clinical evaluation of intranasal vaccines in Phase I trials involving HPIV-seronegative infants and children.
Main Results:
- Two HPIV3 vaccine candidates demonstrated good tolerability, infectivity, and immunogenicity in Phase I trials.
- Vaccines targeting HPIV1 and HPIV2 are in earlier stages of development, having recently entered pediatric trials.
Conclusions:
- Live-attenuated intranasal HPIV3 vaccines are safe and immunogenic in infants and children, warranting further clinical investigation.
- Continued development of HPIV1 and HPIV2 vaccines is necessary to provide comprehensive protection against HPIV-associated respiratory diseases.
Abstract:
In children under 5 years of age, human parainfluenza viruses (HPIVs) as a group are the second most common etiology of acute respiratory illness leading to hospitalization, surpassed only by respiratory syncytial virus but ahead of influenza viruses. Using reverse genetics systems for HPIV serotypes 1, 2 and 3 (HPIV1, 2 and 3), several live-attenuated HPIVs have been generated and evaluated as intranasal vaccines in adults and in children. Two vaccines against HPIV3 were found to be well tolerated, infectious and immunogenic in Phase I trials in HPIV3-seronegative infants and children and should progress to proof-of-concept trials. Vaccines against HPIV1 and HPIV2 are less advanced and have just entered pediatric trials.
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