Heterologous prime-boost vaccination using an AS03B-adjuvanted influenza A(H5N1) vaccine in infants and children<3 years of age.

Terry Nolan, Patricia Izurieta, Bee-Wah Lee, Poh Chong Chan, Helen Marshall, Robert Booy, Mamadou Drame, David W Vaughn

Journal: The Journal of infectious diseases 2015;210(11):1800-10

PMID: 24973461

Abstract

BACKGROUND

Protecting young children from pandemic influenza should also reduce transmission to susceptible adults, including pregnant women.

METHODS

An open study assessed immunogenicity and reactogenicity of a heterologous booster dose of A/turkey/Turkey/1/2005(H5N1)-AS03B (AS03B is an Adjuvant System containing α-tocopherol and squalene in an oil-in-water emulsion [5.93 mg tocopherol]) in infants and children aged 6 to <36 months that was given 6 months following 2-dose primary vaccination with A/Indonesia/05/2005(H5N1)-AS03B. Vaccines contained 1.9 µg of hemagglutinin antigen and AS03B. Hemagglutinin inhibition (HI) responses, microneutralization titers, and antineuraminidase antibody levels were assessed for 6 months following the booster vaccination.

RESULTS

For each age stratum (defined on the basis of the subject's age at first vaccination as 6 to <12 months, 12 to <24 months, and 24 to <36 months) and overall (n=113), European influenza vaccine licensure criteria were fulfilled for responses to A/turkey/Turkey/1/2005(H5N1) 10 days following the booster vaccination. Local pain and fever increased with consecutive doses. Anamnestic immune responses were demonstrated for HI, neutralizing, and antineuraminidase antibodies against vaccine-homologous/heterologous strains. Antibody responses to vaccine-homologous/heterologous strains persisted in all children 6 months following the booster vaccination.

CONCLUSIONS

Prevaccination of young children with a clade 2 strain influenza A(H5N1) AS03-adjuvanted vaccine followed by heterologous booster vaccination boosted immune responses to the homologous strain and a related clade, with persistence for at least 6 months. The results support a prime-boost vaccination approach in young children for pandemic influenza preparedness.

CLINICAL TRIALS REGISTRATION

NCT01323946.

© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America.

Address: Murdoch Childrens Research Institute Melbourne School of Population and Global Health, University of Melbourne, Victoria.; GlaxoSmithKline Vaccines, Wavre.; Mount Elizabeth Medical Centre.; National University Hospital, Singapore.; Vaccinology and Immunology Research Trials Unit, Women's and Children's Hospital, North Adelaide School of Paediatrics and Reproductive Health Robinson Research Institute, University of Adelaide.; Children's Hospital at Westmead, National Centre for Immunisation Research and Surveillance, Australia.; GlaxoSmithKline Vaccines, King of Prussia, Pennsylvania.; GlaxoSmithKline Vaccines, Rixensart, Belgium.
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