TLR7 ligand-cyclodextrin conjugate is a promising adjuvant for intranasal influenza vaccine

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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Publication Details

Journal
Vaccine
Published
2026-05-27
DOI
https://doi.org/10.1016/j.vaccine.2026.128762
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

TLR7 ligand-cyclodextrin conjugate is a promising adjuvant for intranasal influenza vaccine

Tomoko Hayashi, Michael Chan, Yasuo Suda, Masahiro Wakao et al.
Vaccine
Influenza Virus Research Studies
article

TLR7 ligand-cyclodextrin conjugate is a promising adjuvant for intranasal influenza vaccine

Tomoko Hayashi, Michael Chan, Yasuo Suda, Masahiro Wakao, Koki Murata, Howard B. Cottam, Hiroyuki Shinchi, Ryo Jufuku, Dennis A. Carson
article en

Abstract

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.

VaccineVol. 86
Kagoshima University (JP), University of California San Diego (US)
Takahashi Industrial and Economic Research Foundation, Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science, National Institute of Allergy and Infectious Diseases, Adaptable and Seamless Technology Transfer Program through Target-Driven R and D
Good health and well-being
Openalex Percentile: Top 7%
Influenza Virus Research Studies
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