DNA‐Engineered Modular Nanovaccines Featuring Precise Topology for Enhanced Immunogenicity

Multivalent display of antigens can boost subunit vaccine immunogenicity. However, owing to the inherent difficulty in programmatically controlling the topology of multivalent antigens, its impact on antigen immunogenicity remains elusive. In this study, DNA-mediated modular precision assembly is employed to organize SARS-CoV-2 receptor-binding domains (RBDs) with different topological connections while preserving their epitopes. It is found that branching-connected RBDs induced significantly higher IgG titers than linear-connected RBDs at higher antigen valency (≥4). This increase in IgG response is associated with stronger B cell proliferation, likely due to enhanced antigen-receptor synergistic interactions leading to enhanced B cell receptor signaling. Branching-connected RBDs also provided superior humoral immunity in mice and stronger protection in SARS-CoV-2-infected hamsters compared to adjuvanted RBD. This work highlights the role of antigen topology in vaccine design and offers a universal modular platform for producing more effective subunit vaccines.

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Publication Details

Journal
Advanced Materials
Published
2025-05-15
DOI
https://doi.org/10.1002/adma.202500577
Citations
3
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
2.42

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DNA‐Engineered Modular Nanovaccines Featuring Precise Topology for Enhanced Immunogenicity

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Advanced Materials
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article

DNA‐Engineered Modular Nanovaccines Featuring Precise Topology for Enhanced Immunogenicity

Fengyun Shen, Chunhai Fan, Binghui Xia, Yun‐Long Zhang, Yanfei Qu, Itamar Willner, Ying Zhu, Dawei Wang, Xiurong Yang, Lihua Wang, Qisheng Wang, Qin Xu, Lele Sun, Huating Kong
article en
3 citations

Abstract

Multivalent display of antigens can boost subunit vaccine immunogenicity. However, owing to the inherent difficulty in programmatically controlling the topology of multivalent antigens, its impact on antigen immunogenicity remains elusive. In this study, DNA-mediated modular precision assembly is employed to organize SARS-CoV-2 receptor-binding domains (RBDs) with different topological connections while preserving their epitopes. It is found that branching-connected RBDs induced significantly higher IgG titers than linear-connected RBDs at higher antigen valency (≥4). This increase in IgG response is associated with stronger B cell proliferation, likely due to enhanced antigen-receptor synergistic interactions leading to enhanced B cell receptor signaling. Branching-connected RBDs also provided superior humoral immunity in mice and stronger protection in SARS-CoV-2-infected hamsters compared to adjuvanted RBD. This work highlights the role of antigen topology in vaccine design and offers a universal modular platform for producing more effective subunit vaccines.

Advanced MaterialsVol. 37(30)
Shanghai University (CN), Shanghai Jiao Tong University (CN), Hebrew University of Jerusalem (IL), Chinese Academy of Sciences (CN), Shanghai Advanced Research Institute (CN)
Natural Science Foundation of Shanghai, National Natural Science Foundation of China, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 12%
Advanced biosensing and bioanalysis techniques
2.42
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