Abstract

Bacillus Calmette-Guerin (BCG) and the cell wall skeleton (CWS) derived from BCG are known to enhance nonspecific immune activation and anti-cancer immunity; however, their roles as a vaccine adjuvant are largely unknown. Here, we report that BCG-CWS acts as a strong immune adjuvant by promoting the protective immune responses in mouse models with influenza vaccination. The different aged mice immunized with inactivated split vaccine with or without BCG-CWS were challenged with an influenza pandemic virus. When protective immune responses were compared, even a single immunization of adult mice with a BCG-CWS-adjuvanted vaccine showed significantly enhanced humoral immune responses with increased IgG1 and IgG2a isotype antibodies. Importantly, the protective effects by the BCG-CWS adjuvant for influenza vaccination upon humoral and cellular immunogenicity were comparable between infants (6 days and 2 weeks old) and aged (20 months old) mice. Moreover, BCG-CWS dramatically augmented vaccine-mediated protective responses, including decreased viral loads, lung damage, and airway resistance, as well as increased mouse survival, amelioration of weight loss, and proinflammatory cytokine expression in all experimental groups including infant, adults, and old aged mice. We further provided the evidence that the BCG-CWS adjuvant effects were mediated through Toll-like receptors (TLR) 2 and TLR4 signaling pathways. Together, these data suggest that BCG-CWS can be promising as a potential influenza vaccine adjuvant in both young and old aged population through TLR2/4-mediated immune-boosting activities.

Highlights

  • We investigated Bacillus Calmette-Guerin (BCG)-cell wall skeleton (CWS) adjuvant effects on influenza vaccine efficacy in neonatal infant ages (6 D, 2 W), adult, and old (20 M) age mice after priming and/or boosting by intramuscular vaccination with an inactivated split vaccine prior to challenge with influenza virus infection

  • It was expected that CWS would have prominent adjuvant effects in a single dose vaccination with inactivated influenza virus in adult BALB/c mice

  • Toll-like receptor 2 (TLR2) and TLR4 knockout mice significantly reduced the production of tumor necrosis factor (TNF)-α and interleukin 6 (IL-6) than those from wild type mice did, after BCG-CWS stimulation (Figure 8A,B). These results suggest that BCG-CWS exhibits stimulating effects in antigen presenting cells (APCs) through induction of inflammatory cytokines via TLR2 and TLR4 signaling pathways

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Summary

Introduction

An attenuated Mycobacterium bovis Bacillus Calmette-Guerin (BCG), a safe and licensed live attenuated vaccine for human tuberculosis, has been implemented in international vaccination programs since the 1920s, with proven safety [1]. BCG vaccination of newborns and infants provides various degrees of protection against human tuberculosis caused by Mycobacterium tuberculosis [2]. BCG vaccination and positive tuberculin reaction in early childhood are related to increased survival with nonspecific immune activation and broad protection against other infections [3]. Recent studies suggest that BCG vaccinationinduced non-specific immunity and cross-protection are associated with trained immunity, Biomedicines 2021, 9, 516.

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