An RNA-Scaffold Protein Subunit Vaccine for Nasal Immunization

Author:

Lam Joy-Yan12ORCID,Wong Wan-Man12,Yuen Chun-Kit12ORCID,Ng Yau-Yee1,San Chun-Hin1ORCID,Yuen Kwok-Yung123,Kok Kin-Hang1234ORCID

Affiliation:

1. Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China

2. Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong, China

3. State Key Laboratory for Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China

4. AIDS Institute, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China

Abstract

Developing recombinant proteins as nasal vaccines for inducing systemic and mucosal immunity against respiratory viruses is promising. However, additional adjuvants are required to overcome the low immunogenicity of protein antigens. Here, a self-adjuvanted protein-RNA ribonucleoprotein vaccine was developed and found to be an effective nasal vaccine in mice and the SARS-CoV-2 infection model. The vaccine consisted of spike RBD (as an antigen), nucleoprotein (as an adaptor), and ssRNA (as an adjuvant and RNA scaffold). This combination robustly induced mucosal IgA, neutralizing antibodies and activated multifunctional T-cells, while also providing sterilizing immunity against live virus challenge. In addition, high-resolution scRNA-seq analysis highlighted airway-resident immune cells profile during prime-boost immunization. The vaccine also possesses modularity (antigen/adaptor/RNA scaffold) and can be made to target other viruses. This protein-RNA ribonucleoprotein vaccine is a novel and promising approach for developing safe and potent nasal vaccines to combat respiratory virus infections.

Funder

General Research Fund

Innovation and Technology Commission, the Government of the Hong Kong Special Administrative Region, China

Theme-based Research Scheme

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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