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Analyzing immune responses to varied mRNA and protein vaccine sequences
- Title
- Analyzing immune responses to varied mRNA and protein vaccine sequences
- Authors
- Park; Hyeong-Jun; Bang; Yoo-Jin; Kwon; Sung Pil; Kwak; Woori; Sang-In; Roh; Gahyun; Bae; Seo-Hyeon; Kim; Jae-Yong; Hye Won; Yongkwan; Yoo; Soyeon; Daegeun; Keum; Gyochang; Eun-Kyoung; Hong; So-Hee; Nam; Jae-Hwan
- Ewha Authors
- 홍소희
- SCOPUS Author ID
- 홍소희
- Issue Date
- 2023
- Journal Title
- npj Vaccines
- ISSN
- 2059-0105
- Citation
- npj Vaccines vol. 8, no. 1
- Publisher
- Nature Research
- Indexed
- SCIE; SCOPUS
- Document Type
- Article
- Abstract
- In response to the COVID-19 pandemic, different types of vaccines, such as inactive, live-attenuated, messenger RNA (mRNA), and protein subunit, have been developed against SARS-CoV-2. This has unintentionally created a unique scenario where heterologous prime-boost vaccination against a single virus has been administered to a large human population. Here, we aimed to analyze whether the immunization order of vaccine types influences the efficacy of heterologous prime-boost vaccination, especially mRNA and protein-based vaccines. We developed a new mRNA vaccine encoding the hemagglutinin (HA) glycoprotein of the influenza virus using the 3′-UTR and 5′-UTR of muscle cells (mRNA-HA) and tested its efficacy by heterologous immunization with an HA protein vaccine (protein-HA). The results demonstrated higher IgG2a levels and hemagglutination inhibition titers in the mRNA-HA priming/protein-HA boosting (R-P) regimen than those induced by reverse immunization (protein-HA priming/mRNA-HA boosting, P-R). After the viral challenge, the R-P group showed lower virus loads and less inflammation in the lungs than the P-R group did. Transcriptome analysis revealed that the heterologous prime-boost groups had differentially activated immune response pathways, according to the order of immunization. In summary, our results demonstrate that the sequence of vaccination is critical to direct desired immune responses. This study demonstrates the potential of a heterologous vaccination strategy using mRNA and protein vaccine platforms against viral infection. © 2023, The Author(s).
- DOI
- 10.1038/s41541-023-00684-0
- Appears in Collections:
- 의과대학 > 의학과 > Journal papers
- Files in This Item:
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s41541-023-00684-0.pdf(11.4 MB)
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