tetano
Editor, Senior Moderator
Hum Vaccin Immunother. 2017 Sep 19:0. doi: 10.1080/21645515.2017.1373227. [Epub ahead of print]
[h=1]MF59-adjuvanted influenza vaccine (FLUAD?) elicits higher immune responses than a non-adjuvanted influenza vaccine (Fluzone?): a randomized, multicenter, Phase III pediatric trial in Mexico.[/h] Cruz-Valdez A[SUP]1[/SUP], Valdez-Zapata G[SUP]2[/SUP], Patel SS[SUP]3[/SUP], Castelli FV[SUP]4[/SUP], Garcia MG[SUP]5[/SUP], Jansen WT[SUP]6[/SUP], Arora AK[SUP]7[/SUP], Heijnen E[SUP]8[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The poor immune response elicited by trivalent influenza vaccines (TIVs) in children can be enhanced by the addition of adjuvants. This observer-blind, randomized Phase III trial assessed the immunogenicity and safety of the MF59-adjuvanted trivalent influenza vaccine FLUAD? (aTIV) and a non-adjuvanted TIV, in healthy children (aged 6 to <72 months) from 3 centers in Mexico, during the 2014-2015 season. The primary objectives were to assess the non-inferiority of aTIV to TIV, measured by geometric mean titers (GMTs), and the safety of aTIV and TIV. Seroconversion was one of several secondary objectives. In total, 287 children were enrolled. The non-inferiority criteria for GMTs and seroconversion were met for aTIV for all 3 vaccine strains. Lower bounds of the 95% confidence intervals for all 3 aTIV:TIV vaccine ratios were >2, showing that the immunogenicity of aTIV was superior to that of TIV for all 3 strains. Solicited adverse events (AEs) were experienced more frequently with aTIV than TIV by younger children (aged 6 to <36 months), but were more frequent with TIV than aTIV in older children (aged 36 to <72 months) who had been vaccinated previously. More unsolicited AEs were associated with aTIV than the TIV. All AEs were of mild or moderate severity. No deaths, serious AEs, or AEs leading to premature withdrawal were reported. Overall, aTIV was highly immunogenic and was well tolerated in healthy children 6 to <72 months of age. These results indicate that aTIV may be a beneficial addition to national pediatric vaccination programs.
[h=4]KEYWORDS:[/h] MF59; adjuvant; immunogenicity; influenza; safety; trivalent influenza vaccine
PMID: 28925801 DOI: 10.1080/21645515.2017.1373227
[h=1]MF59-adjuvanted influenza vaccine (FLUAD?) elicits higher immune responses than a non-adjuvanted influenza vaccine (Fluzone?): a randomized, multicenter, Phase III pediatric trial in Mexico.[/h] Cruz-Valdez A[SUP]1[/SUP], Valdez-Zapata G[SUP]2[/SUP], Patel SS[SUP]3[/SUP], Castelli FV[SUP]4[/SUP], Garcia MG[SUP]5[/SUP], Jansen WT[SUP]6[/SUP], Arora AK[SUP]7[/SUP], Heijnen E[SUP]8[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The poor immune response elicited by trivalent influenza vaccines (TIVs) in children can be enhanced by the addition of adjuvants. This observer-blind, randomized Phase III trial assessed the immunogenicity and safety of the MF59-adjuvanted trivalent influenza vaccine FLUAD? (aTIV) and a non-adjuvanted TIV, in healthy children (aged 6 to <72 months) from 3 centers in Mexico, during the 2014-2015 season. The primary objectives were to assess the non-inferiority of aTIV to TIV, measured by geometric mean titers (GMTs), and the safety of aTIV and TIV. Seroconversion was one of several secondary objectives. In total, 287 children were enrolled. The non-inferiority criteria for GMTs and seroconversion were met for aTIV for all 3 vaccine strains. Lower bounds of the 95% confidence intervals for all 3 aTIV:TIV vaccine ratios were >2, showing that the immunogenicity of aTIV was superior to that of TIV for all 3 strains. Solicited adverse events (AEs) were experienced more frequently with aTIV than TIV by younger children (aged 6 to <36 months), but were more frequent with TIV than aTIV in older children (aged 36 to <72 months) who had been vaccinated previously. More unsolicited AEs were associated with aTIV than the TIV. All AEs were of mild or moderate severity. No deaths, serious AEs, or AEs leading to premature withdrawal were reported. Overall, aTIV was highly immunogenic and was well tolerated in healthy children 6 to <72 months of age. These results indicate that aTIV may be a beneficial addition to national pediatric vaccination programs.
[h=4]KEYWORDS:[/h] MF59; adjuvant; immunogenicity; influenza; safety; trivalent influenza vaccine
PMID: 28925801 DOI: 10.1080/21645515.2017.1373227