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Efficacy of genotype-matched vaccine against re-emerging genotype V Japanese encephalitis virus

Authors
 Jae-Deog Kim  ;  Ah-Ra Lee  ;  Dah-Hyun Moon  ;  Young-Uk Chung  ;  Su-Yeon Hong  ;  Hyo Je Cho  ;  Tae Hyun Kang  ;  Yo Han Jang  ;  Myung Hyun Sohn  ;  Baik-Lin Seong  ;  Sang-Uk Seo 
Citation
 EMERGING MICROBES & INFECTIONS, Vol.13(1) : 2343910, 2024-12 
Journal Title
 EMERGING MICROBES & INFECTIONS 
Issue Date
2024-12
MeSH
Animals ; Antibodies, Viral / blood ; Antibodies, Viral / immunology ; Antigens, Viral / genetics ; Antigens, Viral / immunology ; Cholera Toxin / genetics ; Cholera Toxin / immunology ; Encephalitis Virus, Japanese* / classification ; Encephalitis Virus, Japanese* / genetics ; Encephalitis Virus, Japanese* / immunology ; Encephalitis, Japanese* / immunology ; Encephalitis, Japanese* / prevention & control ; Encephalitis, Japanese* / virology ; Female ; Genotype* ; Humans ; Japanese Encephalitis Vaccines* / administration & dosage ; Japanese Encephalitis Vaccines* / genetics ; Japanese Encephalitis Vaccines* / immunology ; Mice ; Mice, Inbred BALB C ; Vaccine Efficacy
Keywords
Japanese encephalitis virus ; genotype V ; neutralizing antibody ; recombinant vaccine ; bivalent vaccine
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.
DOI
10.1080/22221751.2024.2343910
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers
Yonsei Authors
Seong, Baik L(성백린)
Sohn, Myung Hyun(손명현) ORCID logo https://orcid.org/0000-0002-2478-487X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200725
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