Zhou Shi-Hao, Zhang Ru-Yan, You Zi-Wei, Zou Yong-Ke, Wen Yu, Wang Jian, Ding Dong, Bian Miao-Miao, Zhang Zhi-Ming, Yuan Hong, Yang Guang-Fu, Guo Jun
Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, International Joint Research Center for Intelligent Biosensing Technology and Health, Hubei International Scientific and Technological Cooperation Base of Pesticide and Green Synthesis, College of Chemistry, Central China Normal University, Wuhan 430079, China.
ACS Appl Mater Interfaces. 2023 Feb 22;15(7):8914-8926. doi: 10.1021/acsami.2c19736. Epub 2023 Feb 7.
Developing a novel and potent adjuvant with great biocompatibility for immune response augmentation is of great significance to enhance vaccine efficacy. In this work, we prepared a long-term stable, pH-sensitive, and biodegradable Mn(PO)·3HO nanoparticle (nano-MnP) by simply mixing MnCl/NaHPO/NaHPO solution for the first time and employed it as an immune stimulant in the bivalent COVID-19 protein vaccine comprised of wild-type S1 (S1-WT) and Omicron S1 (S1-Omicron) proteins as antigens to elicit a broad-spectrum immunity. The biological experiments indicated that the nano-MnP could effectively activate antigen-presenting cells through the cGAS-STING pathway. Compared with the conventional Alum-adjuvanted group, the nano-MnP-adjuvanted bivalent vaccine elicited approximately 7- and 8-fold increases in IgG antibody titers and antigen-specific IFN-γ secreting T cells, respectively. Importantly, antisera of the nano-MnP-adjuvanted group could effectively cross-neutralize the SARS-CoV-2 and its five variants of concern (VOCs) including Alpha, Beta, Gamma, Delta, and Omicron, demonstrating that this bivalent vaccine based on S1-WT and S1-Omicron proteins is an effective vaccine design strategy to induce broad-spectrum immune responses. Collectively, this nano-MnP material may provide a novel and efficient adjuvant platform for various prophylactic and therapeutic vaccines and provide insights for the development of the next-generation manganese adjuvant.
开发一种具有良好生物相容性的新型强效佐剂以增强免疫反应对于提高疫苗效力具有重要意义。在这项工作中,我们首次通过简单混合MnCl₂/Na₂HPO₄/Na₂HPO₄溶液制备了一种长期稳定、pH敏感且可生物降解的Mn₃(PO₄)₂·3H₂O纳米颗粒(纳米MnP),并将其用作由野生型S1(S1-WT)和奥密克戎S1(S1-Omicron)蛋白作为抗原组成的二价新冠病毒蛋白疫苗中的免疫刺激剂,以引发广谱免疫。生物学实验表明,纳米MnP可通过cGAS-STING途径有效激活抗原呈递细胞。与传统铝佐剂组相比,纳米MnP佐剂二价疫苗分别使IgG抗体滴度和抗原特异性IFN-γ分泌T细胞增加了约7倍和8倍。重要的是,纳米MnP佐剂组的抗血清可有效交叉中和SARS-CoV-2及其包括阿尔法、贝塔、伽马、德尔塔和奥密克戎在内的五种关注变体(VOC),表明这种基于S1-WT和S1-Omicron蛋白的二价疫苗是诱导广谱免疫反应的有效疫苗设计策略。总体而言,这种纳米MnP材料可能为各种预防性和治疗性疫苗提供一个新型高效的佐剂平台,并为下一代锰佐剂的开发提供思路。