State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Department of Laboratory Medicine, School of Public Health, Xiamen University. Xiamen 361102, China; National Institute of Diagnostics and Vaccine Development in Infectious Diseases, State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, Collaborative Innovation Center of Biologic Products, National Innovation Platform for Industry-Education Integration in Vaccine Research, NMPA Key Laboratory for Research and Evaluation of Infectious Disease Diagnostic Technology, the Research Unit of Frontier Technology of Structural Vaccinology of Chinese Academy of Medical Sciences, Xiamen University, Xiamen 361102, China; Novel Product R&D Department,Xiamen Innovax Biotech Co., Ltd., Xiamen 361022, Fujian, China.
State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Department of Laboratory Medicine, School of Public Health, Xiamen University. Xiamen 361102, China; National Institute of Diagnostics and Vaccine Development in Infectious Diseases, State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, Collaborative Innovation Center of Biologic Products, National Innovation Platform for Industry-Education Integration in Vaccine Research, NMPA Key Laboratory for Research and Evaluation of Infectious Disease Diagnostic Technology, the Research Unit of Frontier Technology of Structural Vaccinology of Chinese Academy of Medical Sciences, Xiamen University, Xiamen 361102, China.
Vaccine. 2024 May 31;42(15):3514-3521. doi: 10.1016/j.vaccine.2024.04.056. Epub 2024 Apr 25.
Group A rotavirus (RVA) is the primary etiological agent of acute gastroenteritis (AGE) in children under 5 years of age. Despite the global implementation of vaccines, rotavirus infections continue to cause over 120,000 deaths annually, with a majority occurring in developing nations. Among infants, the P[8] rotavirus strain is the most prevalent and can be categorized into four distinct lineages. In this investigation, we expressed five VP4(aa26-476) proteins from different P[8] lineages of human rotavirus in E. coli and assessed their immunogenicity in rabbits. Among the different P[8] strains, the Wa-VP4 protein, derived from the MT025868.1 strain of the P[8]-1 lineage, exhibited successful purification in a highly homogeneous form and significantly elicited higher levels of neutralizing antibodies (nAbs) against both homologous and heterologous rotaviruses compared to other VP4 proteins derived from different P[8] lineages in rabbits. Furthermore, we assessed the immunogenicity of the Wa-VP4 protein in mice, pigs, and cynomolgus monkeys, observing that it induced robust production of nAbs in all animals. Interestingly, there was no significant difference between in nAb titers against homologous and heterologous rotaviruses in pigs and mankeys. Collectively, these findings suggest that the Wa-VP4* protein may serve as a potential candidate for a rotavirus vaccine.
A 组轮状病毒(RVA)是 5 岁以下儿童急性胃肠炎(AGE)的主要病因。尽管全球已实施疫苗接种,但轮状病毒感染仍每年导致超过 120,000 人死亡,其中大部分发生在发展中国家。在婴儿中,P[8]轮状病毒株最为普遍,可分为四个不同的谱系。在这项研究中,我们在大肠杆菌中表达了来自人类轮状病毒的五个不同 P[8]谱系的 VP4(aa26-476)蛋白,并评估了它们在兔子中的免疫原性。在不同的 P[8]株中,来自 P[8]-1 谱系的 MT025868.1 株的 Wa-VP4 蛋白成功地以高度均一的形式纯化,并显著诱导了针对同源和异源轮状病毒的更高水平的中和抗体(nAbs),与来自不同 P[8]谱系的其他 VP4 蛋白相比,在兔子中。此外,我们评估了 Wa-VP4 蛋白在小鼠、猪和食蟹猴中的免疫原性,观察到它在所有动物中均诱导了强大的 nAb 产生。有趣的是,猪和恒河猴中针对同源和异源轮状病毒的 nAb 滴度之间没有显著差异。总之,这些发现表明 Wa-VP4*蛋白可能是轮状病毒疫苗的潜在候选物。