Related Experiment Video
Updated: Aug 10, 2026

Intranasal Administration of Recombinant Influenza Vaccines in Chimeric Mouse Models to Study Mucosal Immunity
Published on: June 25, 2015
Immunization of high-risk infants younger than 18 months of age with split-product influenza vaccine
J R Groothuis1, M J Levin, G P Rabalais
1Department of Pediatrics, University of Colorado School of Medicine, Denver.
Insights
This study evaluated influenza vaccine safety and effectiveness in high-risk infants. While generally safe, responses varied by age and influenza strain, indicating a need for optimized vaccination strategies for vulnerable children.
Area of Science:
- Pediatric Infectious Diseases
- Vaccinology
- Immunology
Background:
- Influenza poses a significant risk of severe illness in young children with underlying cardiopulmonary conditions.
- Very young children, particularly those with bronchopulmonary dysplasia and congenital heart disease, are a high-risk population for influenza complications.
Purpose of the Study:
- To assess the immunogenicity and safety of an influenza split-product vaccine.
- To evaluate vaccine responses in infants aged 3 to 18 months with specific cardiopulmonary diseases.
Main Methods:
- A 4-year study involving 113 children (3-18 months) with bronchopulmonary dysplasia and congenital heart disease.
- Sera were collected pre- and post-immunization for hemagglutination inhibition testing.
- Adverse reactions were monitored in 95 children.
Main Results:
- Seroresponses were specific to age and influenza antigen, with A/Mississippi (H3N2) showing the highest response (97%).
- Children over 6 months demonstrated better seroresponses to A/Leningrad (H3N2) and B/Victoria compared to younger infants.
- Adverse reactions were infrequent (9%) and predominantly mild.
Conclusions:
- Influenza vaccination is generally safe in this high-risk pediatric population.
- Age and antigen specificity of immune responses highlight the need for tailored immunization strategies.
- Further research is required to understand immunologic mechanisms and optimize influenza prevention in very young, high-risk children.
Abstract:
Influenza is an important cause of serious illness in very young children with cardiopulmonary disease. A 4-year study was conducted at two centers to assess immunogenicity and safety of influenza split-product vaccine in children aged 3 to 18 months with bronchopulmonary dysplasia and congenital heart disease. A total of 113 children were studied: 62 children 3 to 5 months of age and 51 children 6 to 18 months of age. Sera were drawn prior to first and second immunization and 3 weeks after second immunization and were tested by hemagglutination inhibition; protection was defined as greater than 1:32. Ninety-five children were surveyed for adverse reactions. Seroresponses were age and antigen specific. Best responses for all ages were to A/Mississippi (H3N2) (97%). Children older than 6 months of age had better seroresponses to A/Leningrad (H3N2) (73%, P less than .03) and B/Victoria (62%, P less than .02) than did children younger than 6 months of age. Seroconversion rates to the remaining antigens were low. Only 9% of children experienced adverse reactions; all but one were mild. The immunologic mechanisms responsible for preventing serious influenzal disease and more effective immunization strategies need to be defined for very young high-risk children.
Related Concept Videos
Vaccinations
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Drug Dosing: Infants and Children
Smallpox
Influenza
Respiratory Syncytial Virus Disease

