Immunogenicity and safety of MF59-adjuvanted and full-dose unadjuvanted trivalent inactivated influenza vaccines among vaccine-naïve children in a randomized clinical trial in rural Senegal

Aldiouma Diallo, John C Victor, Jodi Feser, Justin R Ortiz, Niranjan Kanesa-Thasan, Moussa Ndiaye, Bou Diarra, Sathie Cheikh, Djibril Diene, Tofene Ndiaye, Assane Ndiaye, Kathryn E Lafond, Marc-Alain Widdowson, Kathleen M Neuzil

Research output: Contribution to journalA1: Web of Science-article

Abstract

INTRODUCTION: Effective, programmatically suitable influenza vaccines are needed for low-resource countries.

MATERIALS AND METHODS: This phase II, placebo-controlled, randomized safety and immunogenicity trial (NCT01819155) was conducted in Senegal using the 2012-2013 Northern Hemisphere trivalent influenza vaccine (TIV) formulation. Participants were allocated in a 2:2:1 ratio to receive TIV (full-dose for all age groups), adjuvanted TIV (aTIV), or placebo. Participants were stratified into age groups: 6-11, 12-35, and 36-71 months. All participants were vaccine-naïve and received two doses of study vaccine 4 weeks apart. The two independent primary objectives were to estimate the immunogenicity of TIV and of aTIV as the proportion of children with a hemagglutination inhibition (HI) antibody titer of ≥1:40 to each vaccine strain at 28 days post-dose two. Safety was evaluated by solicited local and systemic reactions, unsolicited adverse events, and serious adverse events.

RESULTS: 296 children received TIV, aTIV, or placebo, and 235 were included in the final analysis. After two doses, children aged 6-11, 12-35, and 36-71 months receiving TIV had HI titers ≥1:40 against A/H1N1 (73.1%, 94.1%, and 97.0%), A/H3N2 (96.2%, 100.0%, and 100.0%), and B (80.8%, 97.1%, and 97.0%), respectively. After two doses, 100% children aged 6-11, 12-35, and 36-71 months receiving aTIV had ≥1:40 titers against A/H1N1, A/H3N2, and B. After a single dose, the aTIV response was comparable to or greater than the TIV response for all vaccine strains. TIV and aTIV reactogenicity were similar, except for mild elevation in temperature (37.5-38.4 °C) which occurred more frequently in aTIV than TIV after each vaccine dose. TIV and aTIV had similarly increased pain/tenderness at the injection site compared to placebo.

CONCLUSIONS: Both aTIV and full-dose TIV were well-tolerated and immunogenic in children aged 6-71 months. These vaccines may play a role in programmatically suitable strategies to prevent influenza in low-resource settings.

Original languageEnglish
JournalVaccine
Volume36
Issue number43
Pages (from-to)6424-6432
Number of pages9
ISSN0264-410X
DOIs
Publication statusPublished - 2018

Keywords

  • Adjuvants, Immunologic/adverse effects
  • Antibodies, Viral/blood
  • Child, Preschool
  • Female
  • Hemagglutination Inhibition Tests
  • Humans
  • Immunogenicity, Vaccine
  • Infant
  • Influenza A Virus, H1N1 Subtype
  • Influenza A Virus, H3N2 Subtype
  • Influenza Vaccines/adverse effects
  • Influenza, Human/prevention & control
  • Male
  • Polysorbates
  • Senegal
  • Squalene/immunology
  • Vaccines, Inactivated/adverse effects

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