Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Graduate Program in Biomaterials Science and Engineering, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Front Immunol. 2021 Nov 12;12:769088. doi: 10.3389/fimmu.2021.769088. eCollection 2021.
Vaccine adjuvants from natural resources have been utilized for enhancing vaccine efficacy against infectious diseases. This study examined the potential use of catechins, polyphenolic materials derived from green tea, as adjuvants for subunit and inactivated vaccines. Previously, catechins have been documented to have irreversible virucidal function, with the possible applicability in the inactivated viral vaccine platform. In a mouse model, the coadministration of epigallocatechin-3-gallate (EGCG) with influenza hemagglutinin (HA) antigens induced high levels of neutralizing antibodies, comparable to that induced by alum, providing complete protection against the lethal challenge. Adjuvant effects were observed for all types of HA antigens, including recombinant full-length HA and HA1 globular domain, and egg-derived inactivated split influenza vaccines. The combination of alum and EGCG further increased neutralizing (NT) antibody titers with the corresponding hemagglutination inhibition (HI) titers, demonstrating a dose-sparing effect. Remarkably, EGCG induced immunoglobulin isotype switching from IgG1 to IgG2a (approximately >64-700 fold increase), exerting a more balanced T1/T2 response compared to alum. The upregulation of IgG2a correlated with significant enhancement of antibody-dependent cellular cytotoxicity (ADCC) function (approximately 14 fold increase), providing a potent effector-mediated protection in addition to NT and HI. As the first report on a novel class of vaccine adjuvants with built-in virucidal activities, the results of this study will help improve the efficacy and safety of vaccines for pandemic preparedness.
从自然资源中提取的疫苗佐剂已被用于增强针对传染病的疫苗效力。本研究探讨了儿茶素(绿茶中提取的多酚物质)作为亚单位疫苗和灭活疫苗佐剂的潜力。先前已有文献记载儿茶素具有不可逆的抗病毒作用,因此可能适用于灭活病毒疫苗平台。在小鼠模型中,表没食子儿茶素没食子酸酯(EGCG)与流感血凝素(HA)抗原共同给药可诱导高水平的中和抗体,与铝佐剂相当,可完全抵抗致死性挑战。佐剂效应观察到所有类型的 HA 抗原,包括重组全长 HA 和 HA1 球状结构域以及源自鸡蛋的灭活分裂流感疫苗。铝佐剂和 EGCG 的组合进一步提高了中和(NT)抗体滴度和相应的血凝抑制(HI)滴度,显示出剂量节省效应。值得注意的是,EGCG 诱导免疫球蛋白同种型从 IgG1 向 IgG2a 的转换(约增加 64-700 倍),与铝佐剂相比,产生更平衡的 T1/T2 反应。IgG2a 的上调与抗体依赖性细胞毒性(ADCC)功能的显著增强相关(约增加 14 倍),除了 NT 和 HI 之外,还提供了有效的效应细胞介导的保护。作为具有内置抗病毒活性的新型疫苗佐剂的第一个报告,本研究结果将有助于提高大流行性流感疫苗的功效和安全性。