Design and Preclinical Evaluation of a Multi-Epitope mRNA Vaccine Against Methicillin-Resistant Staphylococcus Aureus (MRSA)

Methicillin-resistant Staphylococcus aureus (MRSA) infections represent a critical healthcare challenge. In this study, we describe the design a multi-epitope mRNA vaccine encoding immunodominant MRSA antigens, delivered using a novel lipid nanoparticle system. Preclinical evaluation in murine models demonstrated robust humoral and cellular immune responses, with significant protection against MRSA challenge. The vaccine exhibited excellent safety and tolerability profiles. No bacterial colonies were detected in the brain, lung, and spleen tissues of the mice that were immunized with the mRNA vaccine at dosages of 75, 150, or 300 µg. No statistical difference in bacterial burden was found among the mRNA-dosed groups. Our findings support the further development of mRNA-based strategies for combating antibiotic-resistant bacterial infections.

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Publication Details

Journal
Trends in Pharmaceutical Biotechnology
Published
2025-06-30
DOI
https://doi.org/10.57238/tpb.2025.153196.1025
Citations
1
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
0.81
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article

Design and Preclinical Evaluation of a Multi-Epitope mRNA Vaccine Against Methicillin-Resistant Staphylococcus Aureus (MRSA)

Siti Norhajah Hashim, Qassim A. Zigam, Ahmed R. Ali, Noor Kbah et al.
1 citations
Trends in Pharmaceutical Biotechnology
RNA Interference and Gene Delivery
0.81
article

Design and Preclinical Evaluation of a Multi-Epitope mRNA Vaccine Against Methicillin-Resistant Staphylococcus Aureus (MRSA)

Siti Norhajah Hashim, Qassim A. Zigam, Ahmed R. Ali, Noor Kbah, Fatemah Shkir
article en
1 citations

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) infections represent a critical healthcare challenge. In this study, we describe the design a multi-epitope mRNA vaccine encoding immunodominant MRSA antigens, delivered using a novel lipid nanoparticle system. Preclinical evaluation in murine models demonstrated robust humoral and cellular immune responses, with significant protection against MRSA challenge. The vaccine exhibited excellent safety and tolerability profiles. No bacterial colonies were detected in the brain, lung, and spleen tissues of the mice that were immunized with the mRNA vaccine at dosages of 75, 150, or 300 µg. No statistical difference in bacterial burden was found among the mRNA-dosed groups. Our findings support the further development of mRNA-based strategies for combating antibiotic-resistant bacterial infections.

Trends in Pharmaceutical BiotechnologyVol. 3(1)
Mustansiriyah University (IQ), Mansoura University (EG), University of Babylon (IQ), Alsalam University College (IQ), Al-Zahra College for Women (OM), University of Kerbala (IQ)
Openalex Percentile: Top 25%
RNA Interference and Gene Delivery
0.81
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