Sijing Yan, Fan Yang, Jia Ji, Xiantian Lin, Ping Wang, Han Wu, Linfang Cheng, Fumin Liu, Nanping Wu, Hangping Yao, Wade S. J. Wu, Haibo Wu
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Flow cytometry and enzyme-linked immunospot assays assessed T cell phenotypes and cytokine expression. The protective effects were tested through challenge experiments, and the adjuvants were further evaluated in a quadrivalent seasonal influenza vaccine.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>BCG-PSN adjuvant exhibited favorable safety profiles and demonstrated an ability to elevate total antibody titers, particularly enhancing neutralizing antibody production when co-administered with the H1N1 antigen. BCG-PSN increased cytokine levels and the proportion of CD8+ T lymphocytes, indicating its capacity to enhance cellular immunity. Upon viral challenge in mice, BCG-PSN mitigated the production of inflammatory factors and reduced lung pathology, effectively protecting the mice. Furthermore, BCG-PSN displayed heightened immunogenicity against a mixture of four antigens.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>BCG-PSN is a reliable and efficient adjuvant for influenza vaccines, holding promise for enhancing vaccine efficacy and increasing immune responses.</p>\n </section>\n </div>","PeriodicalId":13544,"journal":{"name":"Influenza and Other Respiratory Viruses","volume":"19 5","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/irv.70118","citationCount":"0","resultStr":"{\"title\":\"Evaluating Bacillus Calmette–Guérin Polysaccharide Nucleic Acid as an Adjuvant for Influenza Vaccines in Mice\",\"authors\":\"Sijing Yan, Fan Yang, Jia Ji, Xiantian Lin, Ping Wang, Han Wu, Linfang Cheng, Fumin Liu, Nanping Wu, Hangping Yao, Wade S. J. Wu, Haibo Wu\",\"doi\":\"10.1111/irv.70118\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>To enhance influenza vaccine efficacy, it is essential to investigate new adjuvants that are both safe and effective. In a recent study utilizing a mouse model, Bacillus Calmette–Guérin polysaccharide nucleic acid (BCG-PSN) emerged as a promising candidate vaccine adjuvant.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>This study evaluated the immunomodulatory effects of BCG-PSN on influenza vaccines hemagglutinin antigen and aluminum adjuvant as controls. Mice were immunized with H1N1 antigen and adjuvants, and serum antibody levels were measured using hemagglutination inhibition, enzyme-linked immunosorbent assay, and microneutralization assays. Flow cytometry and enzyme-linked immunospot assays assessed T cell phenotypes and cytokine expression. The protective effects were tested through challenge experiments, and the adjuvants were further evaluated in a quadrivalent seasonal influenza vaccine.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>BCG-PSN adjuvant exhibited favorable safety profiles and demonstrated an ability to elevate total antibody titers, particularly enhancing neutralizing antibody production when co-administered with the H1N1 antigen. BCG-PSN increased cytokine levels and the proportion of CD8+ T lymphocytes, indicating its capacity to enhance cellular immunity. Upon viral challenge in mice, BCG-PSN mitigated the production of inflammatory factors and reduced lung pathology, effectively protecting the mice. 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Evaluating Bacillus Calmette–Guérin Polysaccharide Nucleic Acid as an Adjuvant for Influenza Vaccines in Mice
Background
To enhance influenza vaccine efficacy, it is essential to investigate new adjuvants that are both safe and effective. In a recent study utilizing a mouse model, Bacillus Calmette–Guérin polysaccharide nucleic acid (BCG-PSN) emerged as a promising candidate vaccine adjuvant.
Methods
This study evaluated the immunomodulatory effects of BCG-PSN on influenza vaccines hemagglutinin antigen and aluminum adjuvant as controls. Mice were immunized with H1N1 antigen and adjuvants, and serum antibody levels were measured using hemagglutination inhibition, enzyme-linked immunosorbent assay, and microneutralization assays. Flow cytometry and enzyme-linked immunospot assays assessed T cell phenotypes and cytokine expression. The protective effects were tested through challenge experiments, and the adjuvants were further evaluated in a quadrivalent seasonal influenza vaccine.
Results
BCG-PSN adjuvant exhibited favorable safety profiles and demonstrated an ability to elevate total antibody titers, particularly enhancing neutralizing antibody production when co-administered with the H1N1 antigen. BCG-PSN increased cytokine levels and the proportion of CD8+ T lymphocytes, indicating its capacity to enhance cellular immunity. Upon viral challenge in mice, BCG-PSN mitigated the production of inflammatory factors and reduced lung pathology, effectively protecting the mice. Furthermore, BCG-PSN displayed heightened immunogenicity against a mixture of four antigens.
Conclusions
BCG-PSN is a reliable and efficient adjuvant for influenza vaccines, holding promise for enhancing vaccine efficacy and increasing immune responses.
期刊介绍:
Influenza and Other Respiratory Viruses is the official journal of the International Society of Influenza and Other Respiratory Virus Diseases - an independent scientific professional society - dedicated to promoting the prevention, detection, treatment, and control of influenza and other respiratory virus diseases.
Influenza and Other Respiratory Viruses is an Open Access journal. Copyright on any research article published by Influenza and Other Respiratory Viruses is retained by the author(s). Authors grant Wiley a license to publish the article and identify itself as the original publisher. Authors also grant any third party the right to use the article freely as long as its integrity is maintained and its original authors, citation details and publisher are identified.