| Literature DB >> 35244125 |
Ru-Yan Zhang1, Xu-Guang Yin1, Shi-Hao Zhou1, Hai-Wei Zhang2, Jie Lu1, Chen-Bin He1, Jian Wang1, Yu Wen1, Yu-Ting Li1, Yan-Ling Liu1, Ran-Ran Feng1, Dong Ding1, Hua-Wei Wei3, Rui Gong2, Guang-Fu Yang1, Jun Guo1.
Abstract
Adjuvants are important components in vaccines to increase the immunogenicity of proteins and induce optimal immunity. In this study, we designed a novel ternary adjuvant system Alum + c-GAMP + poly(I:C) with STING agonist 3,3'-c-GAMP (c-GAMP) and TLR3 agonist poly(I:C) co-adsorbed on the conventional adjuvant aluminum gel (Alum), and further constructed an S1 protein vaccine. Two doses of vaccination with the ternary adjuvant vaccine were sufficient to induce a balanced Th1/Th2 immune response and robust humoral and cellular immunity. Additionally, the ternary adjuvant group had effective neutralizing activity against live virus SARS-CoV-2 and pseudovirus of all variants of concern (alpha, beta, gamma, delta and omicron). These results indicate that the ternary adjuvants have a significant synergistic effect and can rapidly trigger potent immune responses; the combination of the ternary adjuvant system with S1 protein is a promising COVID-19 vaccine candidate.Entities:
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Year: 2022 PMID: 35244125 DOI: 10.1039/d2cc00271j
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222