Evaluation and comparison of immune responses induced by two Mpox mRNA vaccine candidates in mice

免疫系统 牛痘 病毒学 抗原 病毒 抗体 生物 中和抗体 信使核糖核酸 免疫学 重组DNA 基因 生物化学
作者
Xidan Yang,Congxia Hu,Xuetao Yang,Xiu Yang,Xing Hu,Xingyun Wang,Cong Liu,Yuan Yuan,Shouwen Du,Peng George Wang,Jihui Lin
出处
期刊:Journal of Medical Virology [Wiley]
卷期号:95 (10) 被引量:13
标识
DOI:10.1002/jmv.29140
摘要

The epidemic of Mpox virus (MPXV) from May 2022 was once declared as a Public Health Emergency of International Concern by the World Health Organization. Vaccines play an important role in prevention of infectious diseases, and mRNA vaccine technology was proved to be a safe and effective platform with successful application in defense of coronavirus disease 2019. In this study, based on A29L, M1R, A35R, and B6R of MPXV, we developed two MPXV mRNA vaccine candidates, designated as MPXfus and MPXmix. The MPXfus was one-component, in which these four antigen proteins were linked in tandem by flexible linker and encoded by an individual mRNA as a fusion protein. The MPXmix was multicomponent containing four mRNA, and each mRNA encoded one antigen protein respectively. Mice were immunized with equal quality of MPXfus or MPXmix, delivered by lipid nanoparticles for evaluation and comparison of the immune responses induced by these two MPXV vaccine candidates. Results of immune response analyses indicated that both MPXfus and MPXmix could elicit high-level of antigen-specific antibodies and robust cellular immune response in mice. Moreover, results of virus neutralization assays suggested that sera from MPXfus- or MPXmix-immunized mice possessed high neutralizing activities against vaccinia virus. In addition, titers of antigen-specific antibody, levels of cellular immune response, and activities of neutralizing antibody against vaccinia virus induced by MPXfus and MPXmix presented no significant difference. In summary, this study provides valuable insights for further clinical development of one-component and multicomponent mRNA vaccine candidates for the prevention of MPXV and other orthomyxoviruses.

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