Effect of Varying Doses of a Monovalent H7N9 Influenza Vaccine With and Without ASO3 and MF59 Adjuvants on Immune Response: A Randomized Clinical Trial

Human infections with the avian influenza A(H7N9) virus were first reported in China in 2013 and continue to occur. Hemagglutinin H7 administered alone is a poor immunogen necessitating evaluation of adjuvanted H7N9 vaccines. Here, Jackson et al evaluate the immunogenicity and safety of an inactivat...

Full description

Saved in:
Bibliographic Details
Published inJAMA : the journal of the American Medical Association Vol. 314; no. 3; p. 237
Main Authors Jackson, Lisa A, Campbell, James D, Frey, Sharon E, Edwards, Kathryn M, Keitel, Wendy A, Kotloff, Karen L, Berry, Andrea A, Graham, Irene, Atmar, Robert L, Creech, C Buddy, Thomsen, Isaac P, Patel, Shital M, Gutierrez, Andres F, Anderson, Edwin L, El Sahly, Hana M, Hill, Heather, Noah, Diana L, Bellamy, Abbie R
Format Journal Article
LanguageEnglish
Published Chicago American Medical Association 21.07.2015
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Human infections with the avian influenza A(H7N9) virus were first reported in China in 2013 and continue to occur. Hemagglutinin H7 administered alone is a poor immunogen necessitating evaluation of adjuvanted H7N9 vaccines. Here, Jackson et al evaluate the immunogenicity and safety of an inactivated H7N9 vaccine with and without AS03 adjuvant, as well as mixed vaccine schedules that included sequential administration of AS03- and MF59-containing formulations and of adjuvanted and unadjuvanted formulations. The AS03 and MF59 adjuvants augmented the immune responses to 2 doses of an inactivated H7N9 influenza vaccine, with AS03-adjuvanted formulations inducing the highest titers. This study of 2 adjuvants used in influenza vaccine formulations with adjuvant mixed on site provides immunogenicity information that may be informative to influenza pandemic preparedness programs.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0098-7484
1538-3598