Delta Inulin Adjuvant Enhances Plasmablast Generation, Expression of Activation-Induced Cytidine Deaminase and B-Cell Affinity Maturation in Human Subjects Receiving Seasonal Influenza Vaccine

There is a major need for new adjuvants to improve the efficacy of seasonal and pandemic influenza vaccines. Advax is a novel polysaccharide adjuvant based on delta inulin that has been shown to enhance the immunogenicity of influenza vaccine in animal models and human clinical trials. To better und...

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Published inPloS one Vol. 10; no. 7; p. e0132003
Main Authors Li, Lei, Honda-Okubo, Yoshikazu, Li, Connie, Sajkov, Dimitar, Petrovsky, Nikolai
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 15.07.2015
Public Library of Science (PLoS)
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Summary:There is a major need for new adjuvants to improve the efficacy of seasonal and pandemic influenza vaccines. Advax is a novel polysaccharide adjuvant based on delta inulin that has been shown to enhance the immunogenicity of influenza vaccine in animal models and human clinical trials. To better understand the mechanism for this enhancement, we sought to assess its effect on the plasmablast response in human subjects. This pilot study utilised cryopreserved 7 day post-vaccination (7dpv) peripheral blood mononuclear cell samples obtained from a subset of 25 adult subjects from the FLU006-12 trial who had been immunized intramuscularly with a standard dose of 2012 trivalent inactivated influenza vaccine (TIV) alone (n=9 subjects) or combined with 5mg (n=8) or 10mg (n=8) of Advax adjuvant. Subjects receiving Advax adjuvant had increased 7dpv plasmablasts, which in turn exhibited a 2-3 fold higher rate of non-silent mutations in the B-cell receptor CDR3 region associated with higher expression of activation-induced cytidine deaminase (AID), the major enzyme controlling BCR affinity maturation. Together, these data suggest that Advax adjuvant enhances influenza immunity in immunized subjects via multiple mechanisms including increased plasmablast generation, AID expression and CDR3 mutagenesis resulting in enhanced BCR affinity maturation and increased production of high avidity antibody. How Advax adjuvant achieves these beneficial effects on plasmablasts remains the subject of ongoing investigation. Australia New Zealand Clinical Trials Register ACTRN12612000709842 https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=362709.
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Conceived and designed the experiments: LL DS NP. Performed the experiments: LL YHO CL. Analyzed the data: LL NP. Wrote the paper: LL NP. Clinical Trial Investigator: DS.
Competing Interests: LL, YHO, CL and NP are employees of Vaxine Pty Ltd, which has interests in Advax adjuvant. Vaxine Pty Ltd was the trial sponsor for FLU006-­‐12. Vaxine Pty Ltd holds the following patents relating to material pertinent to this study: (Family of International (PCT) Patent Application No. PCT/AU2005/001328 entitled New polymorphic form of inulin and uses thereof and Family of International (PCT) Patent Application No. PCT/EP2012/061748 entitled Enhanced immunological composition). There are no further patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0132003