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Synthesis of a dendritic cell-targeted self-assembled polymeric nanoparticle for selective delivery of mRNA vaccines to elicit enhanced immune responses.
Fan, Chen-Yo; Wang, Szu-Wen; Chung, Cinya; Chen, Jia-Yan; Chang, Chia-Yen; Chen, Yu-Chen; Hsu, Tsui-Ling; Cheng, Ting-Jen R; Wong, Chi-Huey.
Afiliação
  • Fan CY; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Wang SW; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Chung C; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Chen JY; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Chang CY; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Chen YC; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Hsu TL; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Cheng TR; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
  • Wong CH; Genomics Research Center, Academia Sinica Taipei 115 Taiwan.
Chem Sci ; 15(29): 11626-11632, 2024 Jul 24.
Article em En | MEDLINE | ID: mdl-39055027
ABSTRACT
Recent development of SARS-CoV-2 spike mRNA vaccines to control the pandemic is a breakthrough in the field of vaccine development. mRNA vaccines are generally formulated with lipid nanoparticles (LNPs) which are composed of several lipids with specific ratios; however, they generally lack selective delivery. To develop a selective delivery method for mRNA vaccine formulation, we reported here the synthesis of polymeric nanoparticles (PNPs) composed of a guanidine copolymer containing zwitterionic groups and a dendritic cell (DC)-targeted aryl-trimannoside ligand for encapsulation and selective delivery of an mRNA to dendritic cells. A DC-targeted SARS-CoV-2 spike mRNA-PNP vaccine was shown to elicit a stronger protective immune response in mice compared to the traditional mRNA-LNP vaccine and those without the selective delivery design. It is anticipated that this technology is generally applicable to other mRNA vaccines for DC-targeted delivery with enhanced immune response.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article