Epitope-focused vaccine immunogens design using tailored horseshoe-shaped scaffold

The continuous emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants highlights the need to update coronavirus 2019 disease (COVID-19) vaccine components. Epitope-based vaccine designs targeting conserved and immunorecessive regions of SARS-CoV-2 are critically needed. Here, we report an engineered epitope-focused immunogen design based on a novel horseshoe-shaped natural protein scaffold, named ribonuclease inhibitor 1 (RNH1), that can multiply display of conserved neutralizing epitopes from SARS-CoV-2 S2 stem helix. The designed immunogen RNH1-S1139 demonstrates high binding affinity to S2-specific neutralizing antibodies and elicits robust epitope-targeted antibody responses either through homologous or heterologous vaccination regimens. RNH1-S1139 immune serum has been proven to have similar binding ability against SARS-CoV, SARS-CoV-2 and its variants, providing broad-spectrum protection as a membrane fusion inhibitor. Further studies showed that RNH1 has the potential to serve as a versatile scaffold that displays other helical epitopes from various antigens, including respiratory syncytial virus (RSV) F glycoprotein. Our proposed immunogen engineering strategy via tailored horseshoe-shape nano-scaffold supports the continued development of epitope-focused vaccines as part of a next-generation vaccine design.

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Publication Details

Journal
Journal of Nanobiotechnology
Published
2025-02-18
DOI
https://doi.org/10.1186/s12951-025-03200-9
Citations
4
Primary Topic
Respiratory viral infections research
Type
article
Field-Weighted Citation Impact
5.42
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article

Epitope-focused vaccine immunogens design using tailored horseshoe-shaped scaffold

Yudong Wang, Shipo Wu, Xiaodong Zai, Fangxin Zhao et al.
4 citations
Journal of Nanobiotechnology
Respiratory viral infections research
5.42
article

Epitope-focused vaccine immunogens design using tailored horseshoe-shaped scaffold

Yudong Wang, Shipo Wu, Xiaodong Zai, Fangxin Zhao, Zhengshan Chen, Yilong Yang, Xiaolin Wang, Zhiling Zhang, Wanru Zheng, Yue Zhang, Wei Chen, Zhang Zhang, Jing Zhang, Ruihua Li, Yaohui Li, Junjie Xu, Shaoyan Wang
article en
4 citations

Abstract

The continuous emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants highlights the need to update coronavirus 2019 disease (COVID-19) vaccine components. Epitope-based vaccine designs targeting conserved and immunorecessive regions of SARS-CoV-2 are critically needed. Here, we report an engineered epitope-focused immunogen design based on a novel horseshoe-shaped natural protein scaffold, named ribonuclease inhibitor 1 (RNH1), that can multiply display of conserved neutralizing epitopes from SARS-CoV-2 S2 stem helix. The designed immunogen RNH1-S1139 demonstrates high binding affinity to S2-specific neutralizing antibodies and elicits robust epitope-targeted antibody responses either through homologous or heterologous vaccination regimens. RNH1-S1139 immune serum has been proven to have similar binding ability against SARS-CoV, SARS-CoV-2 and its variants, providing broad-spectrum protection as a membrane fusion inhibitor. Further studies showed that RNH1 has the potential to serve as a versatile scaffold that displays other helical epitopes from various antigens, including respiratory syncytial virus (RSV) F glycoprotein. Our proposed immunogen engineering strategy via tailored horseshoe-shape nano-scaffold supports the continued development of epitope-focused vaccines as part of a next-generation vaccine design.

Journal of NanobiotechnologyVol. 23(1)
Czech Academy of Sciences, Institute of Biotechnology (CZ), Lens Technology (China) (CN), Zhejiang University (CN), Phoenix Contact (United States) (US)
Zero hunger
Openalex Percentile: Top 5%
Respiratory viral infections research
5.42
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