Prospect and challenges for the development of multivalent vaccines against hand, foot and mouth diseases

被引:98
作者
Liu, Chia-Chyi [1 ]
Chow, Yen-Hung [1 ]
Chong, Pele [1 ,2 ]
Klein, Michel [3 ]
机构
[1] Natl Hlth Res Inst, Vaccine R&D Ctr, Zhunan Town 350, Miaoli County, Taiwan
[2] China Med Univ, Grad Inst Immunol, Taichung, Taiwan
[3] VaxiBio Inc, Toronto, ON, Canada
关键词
Human enterovirus A (HEV-A); Hand; foot and mouth diseases; Enterovirus; 71; Coxsackievirus; Inactivated whole virion vaccine; Serum-free culture technology; Cross-neutralizing antibody; Immunodominant epitopes; Waning immunity; ENTEROVIRUS; 71; VACCINE; INFECTION; SAFETY; A16; IMMUNOGENICITY; EVOLUTION; EFFICACY; CHILDREN; TAIWAN; CHINA;
D O I
10.1016/j.vaccine.2014.08.064
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Enterovirus 71 (EV71), an emerging neurotropic virus and coxsackieviruses (CV) are the major causative agents of hand, foot and mouth diseases (HFMD). These viruses have become a serious public health threat in the Asia Pacific region. Formalin-inactivated EV71 (FI-EV71) vaccines have been developed, evaluated in human clinical trials and were found to elicit full protection against EV71. Their failure to prevent CVA16 infections could compromise the acceptability of monovalent EV71 vaccines. Bivalent FI-EV71/FI-CVA16 vaccines have been found to elicit strong neutralizing antibody responses against both viruses in animal models but did not protect against CVA6 and CVA10 viral infections in cell culture neutralization assay. In this review, we discuss the critical bottlenecks in the development of multivalent HFMD vaccines, including the selection of vaccine strains, animal models to assess vaccine potency, the definition of end-points for efficacy trials, and the need for improved manufacturing processes to produce affordable vaccines. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6177 / 6182
页数:6
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