Affiliations 

  • 1 Department of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul, Republic of Korea
  • 2 The Interdisciplinary Graduate Program in Integrative Biotechnology & Translational Medicine, Yonsei University, Incheon, Republic of Korea
  • 3 Department of Biochemistry, Chungbuk National University, Cheongju, Republic of Korea
  • 4 Department of Biopharmaceutical Chemistry, Kookmin University, Seoul, Republic of Korea
  • 5 Department of Vaccine Biotechnology, Andong National University, Andong, Republic of Korea
  • 6 Department of Pediatrics, College of Medicine, Yonsei University, Seoul, Republic of Korea
  • 7 Department of Microbiology and Immunology, College of Medicine, Yonsei University, Seoul, Republic of Korea
Emerg Microbes Infect, 2024 Dec;13(1):2343910.
PMID: 38618740 DOI: 10.1080/22221751.2024.2343910

Abstract

Japanese encephalitis (JE), caused by the Japanese encephalitis virus (JEV), is a highly threatening disease with no specific treatment. Fortunately, the development of vaccines has enabled effective defense against JE. However, re-emerging genotype V (GV) JEV poses a challenge as current vaccines are genotype III (GIII)-based and provide suboptimal protection. Given the isolation of GV JEVs from Malaysia, China, and the Republic of Korea, there is a concern about the potential for a broader outbreak. Under the hypothesis that a GV-based vaccine is necessary for effective defense against GV JEV, we developed a pentameric recombinant antigen using cholera toxin B as a scaffold and mucosal adjuvant, which was conjugated with the E protein domain III of GV by genetic fusion. This GV-based vaccine antigen induced a more effective immune response in mice against GV JEV isolates compared to GIII-based antigen and efficiently protected animals from lethal challenges. Furthermore, a bivalent vaccine approach, inoculating simultaneously with GIII- and GV-based antigens, showed protective efficacy against both GIII and GV JEVs. This strategy presents a promising avenue for comprehensive protection in regions facing the threat of diverse JEV genotypes, including both prevalent GIII and GI as well as emerging GV strains.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.