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  5. Lymph Node Follicle-Targeting STING Agonist Nanoshells Enable Single-Shot M2e Vaccination for Broad and Durable Influenza Protection
 
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Lymph Node Follicle-Targeting STING Agonist Nanoshells Enable Single-Shot M2e Vaccination for Broad and Durable Influenza Protection

Journal
Advanced Science
Date Issued
2023-01-01
Author(s)
Tsai, Hsiao Han
Huang, Ping Han
Lin, Leon C.W.
Yao, Bing Yu
Liao, Wan Ting
Pai, Chen Hsueh
Liu, Yu Han
HUI-WEN CHEN  
Hu, Che Ming J.
DOI
10.1002/advs.202206521
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85153307370&doi=10.1002%2fadvs.202206521&partnerID=40&md5=e30961143dbffef4154d1faa8d5f43b4
https://scholars.lib.ntu.edu.tw/handle/123456789/631971
URL
https://api.elsevier.com/content/abstract/scopus_id/85153307370
Abstract
The highly conserved matrix protein 2 ectodomain (M2e) of influenza viruses presents a compelling vaccine antigen candidate for stemming the pandemic threat of the mutation-prone pathogen, yet the low immunogenicity of the diminutive M2e peptide renders vaccine development challenging. A highly potent M2e nanoshell vaccine that confers broad and durable influenza protectivity under a single vaccination is shown. Prepared via asymmetric ionic stabilization for nanoscopic curvature formation, polymeric nanoshells co-encapsulating high densities of M2e peptides and stimulator of interferon genes (STING) agonists are prepared. Robust and long-lasting protectivity against heterotypic influenza viruses is achieved with a single administration of the M2e nanoshells in mice. Mechanistically, molecular adjuvancy by the STING agonist and nanoshell-mediated prolongation of M2e antigen exposure in the lymph node follicles synergistically contribute to the heightened anti-M2e humoral responses. STING agonist-triggered T cell helper functions and extended residence of M2e peptides in the follicular dendritic cell network provide a favorable microenvironment that induces Th1-biased antibody production against the diminutive antigen. These findings highlight a versatile nanoparticulate design that leverages innate immune pathways for enhancing the immunogenicity of weak immunogens. The single-shot nanovaccine further provides a translationally viable platform for pandemic preparedness.
Subjects
follicular dendritic cells; germinal center; lymph node follicle targeting; matrix protein 2 ectodomain antigen; nanoshell; stimulator of interferon genes agonist; universal influenza vaccine
SDGs

[SDGs]SDG3

Publisher
WILEY
Type
journal article

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