Biosynthesis of Self-Assembled Proteinaceous Nanoparticles for Vaccination

Biosynthesis of Self-Assembled Proteinaceous Nanoparticles for Vaccination

© 2020 The Authors. Published by Wiley-VCH GmbH.

Détails bibliographiques
Publié dans:Advanced materials (Deerfield Beach, Fla.). - 1998. - 32(2020), 42 vom: 18. Okt., Seite e2002940
Auteur principal: Pan, Chao (Auteur)
Autres auteurs: Wu, Jun, Qing, Shuang, Zhang, Xiao, Zhang, Lulu, Yue, Hua, Zeng, Ming, Wang, Bin, Yuan, Zheng, Qiu, Yefeng, Ye, Huahu, Wang, Dongshu, Liu, Xiankai, Sun, Peng, Liu, Bo, Feng, Erling, Gao, Xiaoyong, Zhu, Li, Wei, Wei, Ma, Guanghui, Wang, Hengliang
Format: Article en ligne
Langue:English
Publié: 2020
Accès à la collection:Advanced materials (Deerfield Beach, Fla.)
Sujets:Journal Article AB5 toxins biosynthesis conjugate vaccines nanovaccines self-assembled proteins Antigens Proteins
Description
Résumé:© 2020 The Authors. Published by Wiley-VCH GmbH.
Recent years have seen enormous advances in nanovaccines for both prophylactic and therapeutic applications, but most of these technologies employ chemical or hybrid semi-biosynthetic production methods. Thus, production of nanovaccines has to date failed to exploit biology-only processes like complex sequential post-translational biochemical modifications and scalability, limiting the realization of the initial promise for offering major performance advantages and improved therapeutic outcomes over conventional vaccines. A Nano-B5 platform for in vivo production of fully protein-based, self-assembling, stable nanovaccines bearing diverse antigens including peptides and polysaccharides is presented here. Combined with the self-assembly capacities of pentamer domains from the bacterial AB5 toxin and unnatural trimer peptides, diverse nanovaccine structures can be produced in common Escherichia coli strains and in attenuated pathogenic strains. Notably, the chassis of these nanovaccines functions as an immunostimulant. After showing excellent lymph node targeting and immunoresponse elicitation and safety performance in both mouse and monkey models, the strong prophylactic effects of these nanovaccines against infection, as well as their efficient therapeutic effects against tumors are further demonstrated. Thus, the Nano-B5 platform can efficiently combine diverse modular components and antigen cargos to efficiently generate a potentially very large diversity of nanovaccine structures using many bacterial species
Description:Date Completed 14.07.2021
Date Revised 14.07.2021
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202002940