Liu Chia-Chyi, Chow Yen-Hung, Chong Pele, Klein Michel
Vaccine R&D Center, National Health Research Institutes, Zhunan Town 350, Miaoli County, Taiwan.
Vaccine R&D Center, National Health Research Institutes, Zhunan Town 350, Miaoli County, Taiwan; Graduate Institute of Immunology, China Medical University, Taichung, Taiwan.
Vaccine. 2014 Oct 29;32(47):6177-82. doi: 10.1016/j.vaccine.2014.08.064. Epub 2014 Sep 13.
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.
肠道病毒71型(EV71)是一种新出现的嗜神经病毒,柯萨奇病毒(CV)是手足口病(HFMD)的主要病原体。这些病毒已成为亚太地区严重的公共卫生威胁。福尔马林灭活的EV71(FI-EV71)疫苗已研发出来,并在人体临床试验中进行了评估,发现其能引发对EV71的完全保护。它们无法预防CVA16感染可能会影响单价EV71疫苗的可接受性。在动物模型中,二价FI-EV71/FI-CVA16疫苗已被发现能引发针对这两种病毒的强烈中和抗体反应,但在细胞培养中和试验中不能预防CVA6和CVA10病毒感染。在这篇综述中,我们讨论了多价手足口病疫苗研发中的关键瓶颈,包括疫苗毒株的选择、评估疫苗效力的动物模型、疗效试验终点的定义,以及改进生产工艺以生产价格可承受疫苗的必要性。