Antigen‐Targeting Inserted Nanomicelles Guide Pre‐Existing Immunity to Kill Head and Neck Cancer

A significant challenge in cancer therapy is the identification of suitable targets that are specifically and uniformly expressed across heterogeneous tumors. The efficacy of pre-existing antiviral immunity in tumor treatment is limited by the absence of corresponding targets. This study develops a novel platform of antigen-targeted inserted nanomicelles, preS1 (an antigen of hepatitis B virus)-pHLIP nanomicelles, in which tumor-targeting nanomicelles release antigens that label tumor tissue for pre-existing immunity-mediated lysis in situ. In animal models of head and neck cancers, including head and neck squamous cell carcinoma and anaplastic thyroid cancer, preS1-pHLIP nanomicelles effectively inhibited tumor growth, recurrence, and metastasis in animals pre-immunized with preS1. This therapeutic effect is associated with an increase in the proportion of preS1-specific B cells and activated tumor-specific T cells within the tumor microenvironment. Overall, this work has engineered a nanomicelle that can disguise tumor cells as viruses and achieve tumor killing through the pre-existing antiviral immune response. This strategy presents a novel approach for treating tumors with ambiguous therapeutic target profiles.

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Publication Details

Journal
Advanced Science
Published
2025-03-17
DOI
https://doi.org/10.1002/advs.202410629
Citations
2
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
1.59

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article

Antigen‐Targeting Inserted Nanomicelles Guide Pre‐Existing Immunity to Kill Head and Neck Cancer

Xiao Zhao, Gaofeng Hu, Liehao Jiang, Jiajie Xu et al.
2 citations
Advanced Science
Immunotherapy and Immune Responses
1.59
article

Antigen‐Targeting Inserted Nanomicelles Guide Pre‐Existing Immunity to Kill Head and Neck Cancer

Xiao Zhao, Gaofeng Hu, Liehao Jiang, Jiajie Xu, Y L Li, Tiefeng Jin, Lizhuo Zhang, Keman Cheng, Zhangguo Ying, Xinyang Ge, Chuanming Zheng, Dan Wang, Qinglin Li, Qingqing Feng, Jiafeng Wang, Minghua Ge, Zhuo Tan
article en
2 citations

Abstract

A significant challenge in cancer therapy is the identification of suitable targets that are specifically and uniformly expressed across heterogeneous tumors. The efficacy of pre-existing antiviral immunity in tumor treatment is limited by the absence of corresponding targets. This study develops a novel platform of antigen-targeted inserted nanomicelles, preS1 (an antigen of hepatitis B virus)-pHLIP nanomicelles, in which tumor-targeting nanomicelles release antigens that label tumor tissue for pre-existing immunity-mediated lysis in situ. In animal models of head and neck cancers, including head and neck squamous cell carcinoma and anaplastic thyroid cancer, preS1-pHLIP nanomicelles effectively inhibited tumor growth, recurrence, and metastasis in animals pre-immunized with preS1. This therapeutic effect is associated with an increase in the proportion of preS1-specific B cells and activated tumor-specific T cells within the tumor microenvironment. Overall, this work has engineered a nanomicelle that can disguise tumor cells as viruses and achieve tumor killing through the pre-existing antiviral immune response. This strategy presents a novel approach for treating tumors with ambiguous therapeutic target profiles.

Advanced ScienceVol. 12(18)
IE University (ES), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), University of Macau (MO), Peking Union Medical College Hospital (CN), Zhejiang Cancer Hospital (CN), Zhejiang Provincial People's Hospital (CN), Zhejiang Center for Disease Control and Prevention (CN), National Center for Nanoscience and Technology (CN), Hangzhou Medical College (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality, National Key Research and Development Program of China, Natural Science Foundation of Zhejiang Province
Good health and well-being
Openalex Percentile: Top 18%
Immunotherapy and Immune Responses
1.59
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