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Updated: May 20, 2026

An Optimized Hemagglutination Inhibition (HI) Assay to Quantify Influenza-specific Antibody Titers
Published on: December 1, 2017
Safety and immune responses in children after concurrent or sequential 2009 H1N1 and 2009-2010 seasonal trivalent
Sharon E Frey1, David I Bernstein, Michael A Gerber
1Division of Infectious Diseases, Allergy and Immunology, Saint Louis University School of Medicine, St. Louis, MO 63104, USA. freyse@slu.edu
Insights
In 2009, children received either one or two doses of the monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) alongside the seasonal trivalent inactivated influenza vaccine (TIV). The study found that vaccine combinations were safe and generally well-tolerated across all age groups.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Seasonal and pandemic influenza vaccines were administered separately in 2009.
- A randomized trial was conducted to evaluate combined influenza vaccine administration in children.
Purpose of the Study:
- To assess the safety and immunogenicity of sequential or concurrent administration of 2009 H1N1 influenza vaccine and seasonal trivalent inactivated influenza vaccine (TIV) in children.
- To determine optimal dosing of the 2009 H1N1 vaccine based on age.
Main Methods:
- A randomized trial involving 531 children stratified by age.
- Four study groups received different combinations of one dose of TIV and two doses of 2009 H1N1 vaccine.
- Hemagglutination inhibition antibody responses, reactogenicity, and adverse events were monitored.
Main Results:
- All vaccine combinations were safe and generally well-tolerated.
- One dose of 2009 H1N1 vaccine and one dose of TIV were immunogenic in children aged 10 years and older.
- Children younger than 10 years required two doses of the 2009 H1N1 vaccine for an adequate immune response.
Conclusions:
- The sequence of vaccine administration did not impact 2009 H1N1 vaccine immunogenicity but affected TIV antibody titers.
- Two doses of the 2009 H1N1 vaccine were necessary for protective immunity in children under 10.
- Combined influenza vaccination strategies were safe and effective in pediatric populations.
Background:
Administering 2 separate vaccines for seasonal and pandemic influenza was necessary in 2009. Therefore, we conducted a randomized trial of monovalent 2009 H1N1 influenza vaccine (2009 H1N1 vaccine) and seasonal trivalent inactivated influenza vaccine (TIV; split virion) given sequentially or concurrently in previously vaccinated children.
Methods:
Children randomized to 4 study groups and stratified by age received 1 dose of seasonal TIV and 2 doses of 2009 H1N1 vaccine in 1 of 4 combinations. Injections were given at 21-day intervals and serum samples for hemagglutination inhibition antibody responses were obtained prior to and 21 days after each vaccination. Reactogenicity and adverse events were monitored.
Results:
All combinations of vaccines were safe in the 531 children enrolled. Generally, 1 dose of 2009 H1N1 vaccine and 1 dose of TIV, regardless of sequence or concurrency of administration, was immunogenic in children ≥ 10 years of age; children <10 years of age required 2 doses of 2009 H1N1 vaccine.
Conclusions:
Vaccines were generally well tolerated. The immune responses to 2009 H1N1 vaccine were adequate regardless of the sequence of vaccination in all age groups but the sequence affected titers to TIV antigens. Two doses of 2009 H1N1 vaccine were required to achieve a protective immune response in children <10 years of age.
Clinical Trials Registration:
NCT00943202.
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