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Intranasal Administration of Recombinant Influenza Vaccines in Chimeric Mouse Models to Study Mucosal Immunity
Published on: June 25, 2015
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Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models
Haiqiang Yang1, Jessica Cao2, Xiaoyang Lin1
1Department of Pharmaceutical Sciences, Taneja College of Pharmacy, University of South Florida, Tampa, FL 33612, USA.
Viruses
|March 26, 2022
Summary
A novel peptide-based vaccine shows promise for preventing COVID-19 by inducing durable antibody and T cell responses. This vaccine approach offers flexibility against new SARS-CoV-2 variants and avoids autoimmune issues.
Area of Science:
- Immunology
- Vaccinology
- Molecular Biology
Background:
- Coronavirus disease 2019 (COVID-19) poses significant global health and economic challenges.
- Current vaccines offer protection but face uncertainties regarding long-term efficacy and effectiveness against emerging SARS-CoV-2 variants.
Purpose of the Study:
- To develop and evaluate a novel peptide-based vaccine for preventing COVID-19.
- To assess the immunogenicity and efficacy of the peptide vaccine in a preclinical mouse model.
Main Methods:
- Selection of 15 B cell epitopes from the SARS-CoV-2 spike protein with in silico HLA affinity prediction.
- Testing of peptide vaccines with QS21 or Al(OH)3 adjuvants in C57BL/6 mice.
- Evaluation of antibody and T cell responses, epitope mapping, and pseudoparticle neutralization assays.
Main Results:
- The peptide-based vaccine elicited robust and sustained antibody responses in mice.
- Adjuvant choice influenced T and B cell responses.
- Antibody profiles in vaccinated mice mimicked those of COVID-19 convalescent individuals.
- Vaccine-induced plasma demonstrated neutralizing activity against SARS-CoV-2.
Conclusions:
- The developed peptide-based vaccine generates durable and effective B and T cell responses.
- This vaccine strategy is adaptable for future SARS-CoV-2 variants.
- The approach holds potential as a safe and effective COVID-19 vaccine, minimizing autoimmune risks.

