Advances in mRNA and other vaccines against MERS-CoV

被引:17
|
作者
Tai, Wanbo
Zhang, Xiujuan
Yang, Yang
Zhu, Jiang
Du, Lanying [1 ]
机构
[1] Georgia State Univ, Inst Biomed Sci, Atlanta, GA 30303 USA
关键词
RESPIRATORY SYNDROME CORONAVIRUS; RECEPTOR-BINDING DOMAIN; PRACTICES INTERIM RECOMMENDATION; PROTECTIVE IMMUNE-RESPONSES; DIPEPTIDYL PEPTIDASE 4; UNITED-STATES; IMMUNIZATION PRACTICES; ADVISORY-COMMITTEE; COVID-19; VACCINE; STRUCTURAL DEFINITION;
D O I
10.1016/j.trsl.2021.11.007
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Middle East respiratory syndrome coronavirus (MERS-CoV) is a highly pathogenic human coronavirus (CoV). Belonging to the same beta-CoV genus as severe acute respiratory syndrome coronavirus-1 (SARS-CoV-1) and SARS-CoV-2, MERS-CoV has a significantly higher fatality rate with limited human-to-human transmissibility. MERS-CoV causes sporadic outbreaks, but no vaccines have yet been approved for use in humans, thus calling for continued efforts to develop effective vaccines against this important CoV. Similar to SARS-CoV-1 and SARS-CoV-2, MERS-CoV contains 4 structural proteins, among which the surface spike (S) protein has been used as a core component in the majority of currently developed MERS-CoV vaccines. Here, we illustrate the importance of the MERS-CoV S protein as a key vaccine target and provide an update on the currently developed MERS-CoV vaccines, including those based on DNAs, proteins, virus-like particles or nanoparticles, and viral vectors. Additionally, we describe approaches for designing MERS-CoV mRNA vaccines and explore the role and importance of naturally occurring pseudo -nucleosides in the design of effective MERS-CoV mRNA vaccines. This review also provides useful insights into designing and evaluating mRNA vaccines against other viral pathogens. (Translational Research 2022; 242:20-37)
引用
收藏
页码:20 / 37
页数:18
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