Demonstrates improved antibody responses and protection in mice with intranasal vaccines using TLR7 conjugate adjuvant, indicating its potential.
The development of novel vaccine adjuvants with high efficacy remains an important issue in vaccine design. In this study, we examined a 1 V209-cyclodextrin (CD) conjugate that we have previously developed and evaluated its potential as an adjuvant for intranasal vaccines. Intranasal administration of the vaccines adjuvanted with 1 V209-CD conjugate enhanced both mucosal and systemic IgA and IgG responses against a model antigen, ovalbumin, recombinant hemagglutinin (rHA) from influenza virus strain A/Puerto Rico/8/1934 (H1N1), and a commercially available split influenza vaccine. In an influenza A virus challenge experiment, mice immunized with vaccines adjuvanted with the 1 V209-CD conjugate showed significantly improved survival and reduced lung tissue damage compared with non-adjuvanted controls, indicating that the 1 V209-CD conjugate promoted protective effects. These findings demonstrate that the 1 V209-CD conjugate effectively enhanced immunogenicity of the rHA or existing influenza split vaccine and may serve as a useful adjuvant for intranasal vaccines.
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Jufuku et al. (2026) studied this question.
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