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Design and proof of concept for targeted phage-based COVID-19 vaccination strategies with a streamlined cold-free supply chain
Author(s) -
Daniela I. Staquicini,
Fenny H. F. Tang,
Christopher Markosian,
Virginia J. Yao,
Fernanda I. Staquicini,
Esteban DoderoRojas,
Vinícius G. Contessoto,
Deodate Davis,
Paul E. O’Brien,
Nazia Habib,
Tracey L. Smith,
Natalie Bruiners,
Richard L. Sidman,
Maria Laura Gennaro,
Edmund C. Lattime,
Steven K. Libutti,
Paul C. Whitford,
S.K. Burley,
José N. Onuchic,
Wadih Arap,
Renata Pasqualini
Publication year - 2021
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2105739118
Subject(s) - vaccination , covid-19 , virology , pandemic , authorization , proof of concept , computational biology , biology , computer science , immunology , medicine , computer security , disease , pathology , infectious disease (medical specialty) , operating system
Significance The COVID-19 pandemic has had an unprecedented impact. Although several vaccines have received emergency use authorization, demand has created enormous logistical challenges—including supply, access, and distribution—that justify research for alternative strategies. Phage are viruses that only infect bacteria and can be safely administered to humans. Here, as a proof-of-concept study, we demonstrate that aerosol vaccination with lung-targeted phage particles displaying short SARS-CoV-2 S protein epitopes and subcutaneous vaccination with targeted AAVP particles carrying the entire S protein gene both elicit systemic and specific immune responses in immunocompetent mice. Given their unique attributes, including sturdiness, simple-to-engineer platform, cost-effectiveness for rapid large-scale production, and stability at room temperature, these phage-based approaches may become attractive tools for COVID-19 vaccine development.

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