Development of a novel multi-epitope mRNA vaccine candidate to combat SFTSV pandemic

Severe Fever with Thrombocytopenia Syndrome virus (SFTSV) is a novel identified pathogen, despite two decades of research on SFTSV, the potential widespread threats pose a significant challenge for researchers in developing new treatment and prevention methods. In this present, we have developed a multi-epitope mRNA vaccine for SFTSV and valid it with in silico methods. We screened 9 immunodominant epitopes for cytotoxic T cells (CTL), 7 for helper T cells (HTL), and 8 for Linear B-cell (LBL) based on promising candidate protein Gn, Gc, Np, and NSs. All predicted epitopes demonstrated strong antigenicity without any potential harm to humans. Additionally, the high conservancy is required to cover different strains. All epitopes as well as adjuvants were constructed into a final vaccine, which was further assesd by calculating of physicochemical properties. Then, we docked the vaccine protein with immune receptors and analyzed the complexes with dynamic simulations to evaluate its affinity to receptors. Finally, the vaccine sequence was constructed into a mRNA sequence. The constructed vaccine is a potential candidate for combating SFTSV by stimulating protective humoral and cellular immune responses.

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Publication Details

Journal
PLoS neglected tropical diseases
Published
2025-01-22
DOI
https://doi.org/10.1371/journal.pntd.0012815
Citations
5
Primary Topic
Viral Infections and Vectors
Type
article
Field-Weighted Citation Impact
6.98

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article

Development of a novel multi-epitope mRNA vaccine candidate to combat SFTSV pandemic

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5 citations
PLoS neglected tropical diseases
Viral Infections and Vectors
6.98
article

Development of a novel multi-epitope mRNA vaccine candidate to combat SFTSV pandemic

Caixia Tan, Pinhua Pan, Fei Zhu, Wenzhong Peng, Ziyou Zhou, Shiyang Ma, Hang Yang, Peipei Zhang, Jie Chen, Yizhong Xu
article en
5 citations

Abstract

Severe Fever with Thrombocytopenia Syndrome virus (SFTSV) is a novel identified pathogen, despite two decades of research on SFTSV, the potential widespread threats pose a significant challenge for researchers in developing new treatment and prevention methods. In this present, we have developed a multi-epitope mRNA vaccine for SFTSV and valid it with in silico methods. We screened 9 immunodominant epitopes for cytotoxic T cells (CTL), 7 for helper T cells (HTL), and 8 for Linear B-cell (LBL) based on promising candidate protein Gn, Gc, Np, and NSs. All predicted epitopes demonstrated strong antigenicity without any potential harm to humans. Additionally, the high conservancy is required to cover different strains. All epitopes as well as adjuvants were constructed into a final vaccine, which was further assesd by calculating of physicochemical properties. Then, we docked the vaccine protein with immune receptors and analyzed the complexes with dynamic simulations to evaluate its affinity to receptors. Finally, the vaccine sequence was constructed into a mRNA sequence. The constructed vaccine is a potential candidate for combating SFTSV by stimulating protective humoral and cellular immune responses.

PLoS neglected tropical diseasesVol. 19(1)
Central South University (CN), Hunan Provincial Center for Disease Control and Prevention (CN), National Clinical Research Center for Digestive Diseases (CN), Xiangya Hospital Central South University (CN)
National Natural Science Foundation of China, Central South University, China Postdoctoral Science Foundation, Natural Science Foundation of Hainan Province, Division of Graduate Education
Good health and well-being
Openalex Percentile: Top 4%
Viral Infections and Vectors
6.98
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