Your browser doesn't support javascript.
loading
Immunogenicity of trivalent DNA vaccine candidate encapsulated in Chitosan-TPP nanoparticles against EV-A71 and CV-A16.
Yew, Jia Sheng; Ong, Seng-Kai; Lim, Hui Xuan; Tan, Soon Hao; Ong, Kien Chai; Wong, Kum Thong; Poh, Chit Laa.
Afiliação
  • Yew JS; Centre for Virus & Vaccine Research, School of Medical & Life Sciences, Sunway University, Petaling Jaya, 47500, Malaysia.
  • Ong SK; Department of Biological science, School of Medical & Life Sciences, Sunway University, Petaling Jaya, 47500, Malaysia.
  • Lim HX; Centre for Virus & Vaccine Research, School of Medical & Life Sciences, Sunway University, Petaling Jaya, 47500, Malaysia.
  • Tan SH; Sunway Microbiome Centre, School of Medical & Life Sciences, Sunway University, Petaling Jaya, 47500, Malaysia.
  • Ong KC; Department of Biomedical Science, Faculty of Medicine, Universiti Malaya, Federal Territory of Kuala Lumpur, Kuala Lumpur, 50603, Malaysia.
  • Wong KT; Department of Biomedical Science, Faculty of Medicine, Universiti Malaya, Federal Territory of Kuala Lumpur, Kuala Lumpur, 50603, Malaysia.
  • Poh CL; Department of Pathology, Faculty of Medicine, Universiti Malaya, Federal Territory of Kuala Lumpur, Kuala Lumpur, 50603, Malaysia.
Nanomedicine (Lond) ; 19(21-22): 1779-1799, 2024.
Article em En | MEDLINE | ID: mdl-39140594
ABSTRACT

Aim:

To develop a trivalent DNA vaccine candidate encapsulated in Chitosan-TPP nanoparticles against hand foot and mouth disease (HFMD) and assess its immunogenicity in mice.Materials &

methods:

Trivalent plasmid carrying the VP1 and VP2 genes of EV-A71, VP1 gene of CV-A16 was encapsulated in Chitosan-TPP nanoparticles through ionic gelation. In vitro characterization and in vivo immunization studies of the CS-TPP-NPs (pIRES-VP121) were performed.

Results:

Mice administered with CS-TPP NPs (pIRES-VP121) intramuscularly were observed to have the highest IFN-γ response. Sera from mice immunized with the naked pDNA and CS-TPP-NPs (pIRES-VP121) demonstrated good viral clearance against wild-type EV-A71 and CV-A16 in RD cells.

Conclusion:

CS-TPP-NPs (pIRES-VP121) could serve as a prototype for future development of multivalent HFMD DNA vaccine candidates.
[Box see text].
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas de DNA / Enterovirus Humano A / Quitosana / Nanopartículas / Doença de Mão, Pé e Boca Limite: Animals / Female / Humans Idioma: En Revista: Nanomedicine (Lond) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Malásia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas de DNA / Enterovirus Humano A / Quitosana / Nanopartículas / Doença de Mão, Pé e Boca Limite: Animals / Female / Humans Idioma: En Revista: Nanomedicine (Lond) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Malásia