mRNA-LNP vaccination orchestrates systemic immunity to control human papillomavirus-positive head and neck squamous cell carcinoma

Messenger RNA (mRNA) vaccines have demonstrated significant potential in cancer immunotherapy by activating both innate and adaptive immunity. However, the detailed cellular and molecular dynamics underpinning these systemic immune responses remain incompletely understood. In this study, we characterized the systemic immune landscape following human papillomavirus (HPV)-targeted mRNA-lipid nanoparticle (LNP) vaccination using single-cell RNA sequencing (scRNA-seq) in a murine model of HPV-positive head and neck squamous cell carcinoma (HNSCC). Our study revealed a coordinated remodeling of the systemic immune landscape, involving the tumor microenvironment (TME), tumor-draining lymph nodes (TDLNs), spleen, and blood. Notably, we pioneered a distinct interferon-stimulated gene (ISG) signature across multiple lymphoid subsets in TDLNs, driven by the LNP component, which contributed to rapid, non-antigen-specific immune activation. Additionally, HPV mRNA-LNP vaccination induced an antigen-specific cycling burst of immune cells that mediated tumor control through a systemic coordination of multi-directional differentiation into anti-tumor cell compositions. These findings enhance our understanding of how mRNA-LNP vaccination orchestrates systemic anti-tumor responses and highlight the therapeutic potential of targeting ISG-expressing and cycling immune cells to improve vaccine efficacy, paving the way for future clinical applications in HPV-related cancers.

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Publication Details

Journal
Molecular Therapy — Nucleic Acids
Published
2025-11-20
DOI
https://doi.org/10.1016/j.omtn.2025.102780
Citations
1
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
0.81
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article

mRNA-LNP vaccination orchestrates systemic immunity to control human papillomavirus-positive head and neck squamous cell carcinoma

Xiangrong Song, Xing Duan, Mengli Zhu, Hai Huang et al.
1 citations
Molecular Therapy — Nucleic Acids
RNA Interference and Gene Delivery
0.81
article

mRNA-LNP vaccination orchestrates systemic immunity to control human papillomavirus-positive head and neck squamous cell carcinoma

Xiangrong Song, Xing Duan, Mengli Zhu, Hai Huang, Stephan Lang, Ke Qiu, Yanling Liang, Danni Cheng, Jadwiga Jabłońska, Minzi Mao, Xingchen Peng, Chuanhuan Jiang, Jianjun Ren, Yan Wang, Sisi Wu, Yufang Rao, Xiuli Shao, Shuai Cheng Li, Li Li, Jun Liu, Huifang Li, Haiyang Wang, Geoffrey Liu, Fei Chen, Wei Xu, Yao Song, Yu Zhao, Yongbo Zheng, Lan Feng
article en
1 citations

Abstract

Messenger RNA (mRNA) vaccines have demonstrated significant potential in cancer immunotherapy by activating both innate and adaptive immunity. However, the detailed cellular and molecular dynamics underpinning these systemic immune responses remain incompletely understood. In this study, we characterized the systemic immune landscape following human papillomavirus (HPV)-targeted mRNA-lipid nanoparticle (LNP) vaccination using single-cell RNA sequencing (scRNA-seq) in a murine model of HPV-positive head and neck squamous cell carcinoma (HNSCC). Our study revealed a coordinated remodeling of the systemic immune landscape, involving the tumor microenvironment (TME), tumor-draining lymph nodes (TDLNs), spleen, and blood. Notably, we pioneered a distinct interferon-stimulated gene (ISG) signature across multiple lymphoid subsets in TDLNs, driven by the LNP component, which contributed to rapid, non-antigen-specific immune activation. Additionally, HPV mRNA-LNP vaccination induced an antigen-specific cycling burst of immune cells that mediated tumor control through a systemic coordination of multi-directional differentiation into anti-tumor cell compositions. These findings enhance our understanding of how mRNA-LNP vaccination orchestrates systemic anti-tumor responses and highlight the therapeutic potential of targeting ISG-expressing and cycling immune cells to improve vaccine efficacy, paving the way for future clinical applications in HPV-related cancers.

Molecular Therapy — Nucleic AcidsVol. 36(4)
University Health Network (CA), City University of Hong Kong (HK), University of Toronto (CA), Sichuan University (CN), Princess Margaret Cancer Centre (CA), West China Hospital of Sichuan University (CN), Essen University Hospital (DE), University of Duisburg-Essen (DE)
Openalex Percentile: Top 21%
RNA Interference and Gene Delivery
0.81
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