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Efficacy of genotype-matched vaccine against re-emerging genotype V Japanese encephalitis virus.
Kim, Jae-Deog; Lee, Ah-Ra; Moon, Dah-Hyun; Chung, Young-Uk; Hong, Su-Yeon; Cho, Hyo Je; Kang, Tae Hyun; Jang, Yo Han; Sohn, Myung Hyun; Seong, Baik-Lin; Seo, Sang-Uk.
Afiliação
  • Kim JD; Department of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul, Republic of Korea.
  • Lee AR; Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Moon DH; Department of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul, Republic of Korea.
  • Chung YU; Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Hong SY; The Interdisciplinary Graduate Program in Integrative Biotechnology & Translational Medicine, Yonsei University, Incheon, Republic of Korea.
  • Cho HJ; Department of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul, Republic of Korea.
  • Kang TH; Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Jang YH; Department of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul, Republic of Korea.
  • Sohn MH; Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Seong BL; Department of Biochemistry, Chungbuk National University, Cheongju, Republic of Korea.
  • Seo SU; Department of Biopharmaceutical Chemistry, Kookmin University, Seoul, Republic of Korea.
Emerg Microbes Infect ; 13(1): 2343910, 2024 Dec.
Article em En | MEDLINE | ID: mdl-38618740
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalite Japonesa / Vacinas contra Encefalite Japonesa / Vírus da Encefalite Japonesa (Espécie) / Genótipo Limite: Animals / Female / Humans Idioma: En Revista: Emerg Microbes Infect Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalite Japonesa / Vacinas contra Encefalite Japonesa / Vírus da Encefalite Japonesa (Espécie) / Genótipo Limite: Animals / Female / Humans Idioma: En Revista: Emerg Microbes Infect Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos