Immunological implications of diverse production approaches for Chikungunya virus-like particle vaccines

被引:5
作者
Thompson, Danielle [1 ]
Metz, Stefan W. [1 ]
Abad, Carmen [1 ]
Beaty, Shannon [1 ]
Warfield, Kelly [1 ]
机构
[1] Emergent BioSolut Inc, 400 Profess Dr, Gaithersburg, MD 20879 USA
关键词
Chikungunya; Virus-like particle; Vaccine; Phylogenetics; Expression platform; Neutralizing antibodies; MONOCLONAL-ANTIBODIES; HUMAN-PAPILLOMAVIRUS; E2; PROTEIN; RESPONSES; CELLS; ALPHAVIRUS; EXPRESSION; ANTIGEN; EPITOPE; INSECT;
D O I
10.1016/j.vaccine.2022.04.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chikungunya virus (CHIKV), an arbovirus from the Alphavirus genus, causes sporadic outbreaks and epidemics and can cause acute febrile illness accompanied by severe long-term arthralgias. Over 20 CHIKV vaccine candidates have been developed over the last two decades, utilizing a wide range of vaccine platforms, including virus-like particles (VLP). A CHIKV VLP vaccine candidate is among three candidates in late-stage clinical testing and has potentially promising data in nonclinical and clinical studies exploring safety and vaccine immunogenicity. Despite the consistency of the CHIKV VLP structure, vaccine candidates vary significantly in protein sequence identity, structural protein expression cassettes and their mode of production. Here, we explore the impact of CHIKV VLP coding sequence variation and the chosen expression platform, which affect VLP expression yields, antigenicity and overall vaccine immunogenicity. Additionally, we explore the potential of the CHIKV VLP platform to be modified to elicit protection against other pathogens. (c) 2022 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:3009 / 3017
页数:9
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