In vivo neutrophils hitchhiking for tumor targeting and microenvironment regulation boosts oncolytic virus therapy

Neutrophils constitute a substantial proportion of the immune cell population infiltrating tumors, where they play a pivotal role in establishing an immunosuppressive microenvironment to facilitate tumor growth. Our clinical investigation has unveiled that, following oncolytic virus (OV) treatment, immunosuppressive neutrophils could lead to T cell exhaustion and compromised antitumor efficacy. In this study, we devise a dual-functional conjugation strategy that enables OVs to selectively bind with circulating neutrophils and initiate their death. Prior to dysfunction, neutrophils can harbor OVs and facilitate their infiltration into tumors, leading to a 5.38-fold increase in OV levels within tumors compared to direct intravenous injection. Additionally, infiltrated neutrophils undergo dying after 8 h, which promotes T cell priming, reduces T cell exhaustion, and remodels the tumor immune microenvironment. Our findings illuminate the determinants influencing the efficacy of OVs and propose targeted solutions, thereby offering insights for the clinical translation of these therapeutic agents.

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Publication Details

Journal
Cell Reports Medicine
Published
2025-08-25
DOI
https://doi.org/10.1016/j.xcrm.2025.102314
Citations
2
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
3.63

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article

In vivo neutrophils hitchhiking for tumor targeting and microenvironment regulation boosts oncolytic virus therapy

Xu Zhao, Zhenguo Cheng, Yang Yu, Funan Liu et al.
2 citations
Cell Reports Medicine
Virus-based gene therapy research
3.63
article

In vivo neutrophils hitchhiking for tumor targeting and microenvironment regulation boosts oncolytic virus therapy

Xu Zhao, Zhenguo Cheng, Yang Yu, Funan Liu, Yaohe Wang, Pengliang Wang, Hongjun Li, Mingyang Liu, Han-Wei Huang, Fengming Liu, Zhiqing Pang, Shuhui Song
article en
2 citations

Abstract

Neutrophils constitute a substantial proportion of the immune cell population infiltrating tumors, where they play a pivotal role in establishing an immunosuppressive microenvironment to facilitate tumor growth. Our clinical investigation has unveiled that, following oncolytic virus (OV) treatment, immunosuppressive neutrophils could lead to T cell exhaustion and compromised antitumor efficacy. In this study, we devise a dual-functional conjugation strategy that enables OVs to selectively bind with circulating neutrophils and initiate their death. Prior to dysfunction, neutrophils can harbor OVs and facilitate their infiltration into tumors, leading to a 5.38-fold increase in OV levels within tumors compared to direct intravenous injection. Additionally, infiltrated neutrophils undergo dying after 8 h, which promotes T cell priming, reduces T cell exhaustion, and remodels the tumor immune microenvironment. Our findings illuminate the determinants influencing the efficacy of OVs and propose targeted solutions, thereby offering insights for the clinical translation of these therapeutic agents.

Cell Reports MedicineVol. 6(9)
Sun Yat-sen University (CN), Queen Mary University of London (GB), Fudan University (CN), Sun Yat-sen Memorial Hospital (CN), Shanghai Advanced Research Institute (CN), Ministry of Education (KR), First Hospital of China Medical University (CN), Second Affiliated Hospital of Zhejiang University (CN), Zhejiang University (CN), China Medical University (CN)
National Natural Science Foundation of China, Liaoning Revitalization Talents Program
Zero hunger
Openalex Percentile: Top 7%
Virus-based gene therapy research
3.63
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