| Literature DB >> 27236001 |
Geert Leroux-Roels1, Arnaud Marchant2, Jack Levy3, Pierre Van Damme4, Tino F Schwarz5, Yves Horsmans6, Wolfgang Jilg7, Peter G Kremsner8, Edwige Haelterman9, Frédéric Clément10, Julian J Gabor8, Meral Esen8, Annick Hens4, Isabelle Carletti11, Laurence Fissette11, Fernanda Tavares Da Silva11, Wivine Burny11, Michel Janssens11, Philippe Moris11, Arnaud M Didierlaurent11, Robbert Van Der Most11, Nathalie Garçon11, Pascale Van Belle11, Marcelle Van Mechelen11.
Abstract
Immunogenicity and safety of different adjuvants combined with a model antigen (HBsAg) were compared. Healthy HBV-naïve adults were randomized to receive HBs adjuvanted with alum or Adjuvant Systems AS01B, AS01E, AS03A or AS04 at Days 0 and 30. Different frequencies of HBs-specific CD4+ T cells 14days post dose 2 but similar polyfunctionality profiles were induced by the different adjuvants with frequencies significantly higher in the AS01B and AS01E groups than in the other groups. Antibody concentrations 30days post-dose 2 were significantly higher in AS01B, AS01E and AS03A than in other groups. Limited correlations were observed between HBs-specific CD4+ T cell and antibody responses. Injection site pain was the most common solicited local symptom and was more frequent in AS groups than in alum group. Different adjuvants formulated with the same antigen induced different adaptive immune responses and reactogenicity patterns in healthy naïve adults. The results summary for this study (GSK study number 112115 - NCT# NCT00805389) is available on the GSK Clinical Study Register and can be accessed at www.gsk-clinicalstudyregister.com.Entities:
Keywords: Adaptive immune response; Adjuvant system; CD4(+) T cell; Hepatitis B virus surface antigen; Memory B cell; Polyfunctionality
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Year: 2016 PMID: 27236001 DOI: 10.1016/j.clim.2016.05.007
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969