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不同佐剂对基于蛋白质的亚单位疫苗引发的针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)及其德尔塔变种的免疫反应的影响。

Effect of Different Adjuvants on Immune Responses Elicited by Protein-Based Subunit Vaccines against SARS-CoV-2 and Its Delta Variant.

作者信息

Zhang Naru, Ji Qianting, Liu Zezhong, Tang Kaiming, Xie Yubin, Li Kangchen, Zhou Jie, Li Sisi, Shang Haotian, Shi Zecan, Zheng Tianyu, Yao Jiawei, Lu Lu, Yuan Shuofeng, Jiang Shibo

机构信息

School of Medicine and Waikato Joint Institute, Zhejiang University City College, Hangzhou 310015, China.

Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), Shanghai Frontiers Science Center of Pathogenic Microbes and Infection, School of Basic Medical Sciences, Shanghai Institute of Infectious Disease and Biosecurity, Fudan University, Shanghai 200032, China.

出版信息

Viruses. 2022 Feb 28;14(3):501. doi: 10.3390/v14030501.

Abstract

The global pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become more serious because of the continuous emergence of variants of concern (VOC), thus calling for the development of broad-spectrum vaccines with greater efficacy. Adjuvants play important roles in enhancing the immunogenicity of protein-based subunit vaccines. In this study, we compared the effect of three adjuvants, including aluminum, nanoparticle manganese and MF59, on the immunogenicity of three protein-based COVID-19 vaccine candidates, including RBD-Fc, RBD and S-trimer. We found that the nanoparticle manganese adjuvant elicited the highest titers of SARS-CoV-2 RBD-specific IgG, IgG1 and IgG2a, as well as neutralizing antibodies against infection by pseudotyped SARS-CoV-2 and its Delta variant. What is more, the nanoparticle manganese adjuvant effectively reduced the viral load of the authentic SARS-CoV-2 and Delta variant in the cell culture supernatants. These results suggest that nanoparticle manganese, known to facilitate cGAS-STING activation, is an optimal adjuvant for protein-based COVID-19 subunit vaccines.

摘要

由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)全球大流行,由于值得关注的变异株(VOC)不断出现而变得更加严重,因此需要研发更有效的广谱疫苗。佐剂在增强基于蛋白质的亚单位疫苗的免疫原性方面发挥着重要作用。在本研究中,我们比较了三种佐剂,包括铝、纳米颗粒锰和MF59,对三种基于蛋白质的COVID-19候选疫苗,包括RBD-Fc、RBD和S三聚体的免疫原性的影响。我们发现,纳米颗粒锰佐剂诱导出最高滴度的SARS-CoV-2 RBD特异性IgG、IgG1和IgG2a,以及针对假型SARS-CoV-2及其Delta变异株感染的中和抗体。此外,纳米颗粒锰佐剂有效降低了细胞培养上清液中真实SARS-CoV-2和Delta变异株的病毒载量。这些结果表明,已知可促进cGAS-STING激活的纳米颗粒锰是基于蛋白质的COVID-19亚单位疫苗的最佳佐剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30d3/8950793/48469b8c9d00/viruses-14-00501-g001.jpg

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