Engineered Luminescent Oncolytic Vaccinia Virus Activation of Photodynamic‐Immune Combination Therapy for Colorectal Cancer

Author:

Ye Lu‐Yi123,Li Yi‐Shu3,Ge Tong4,Liu Long‐Cai23,Si Jing‐Xing3,Yang Xue3,Fan Wei‐Jiao13,Liu Xiao‐Zhen3,Zhang You‐Ni4,Wang Jun‐Wei4,Wang Shi‐Bing3,Zou Hai5,Zheng Yue‐Liang1,Jin Ke‐Tao6,Mao Zheng‐Wei17ORCID,Cai Yu123,Mou Xiao‐Zhou1234

Affiliation:

1. Emergency and Critical Care Center Department of Emergency Medicine Zhejiang Provincial People's Hospital (Affiliated People's Hospital) Hangzhou Medical College Hangzhou 310014 China

2. College of Pharmacy Hangzhou Medical College Hangzhou 311300 China

3. Clinical Research Institute Zhejiang Provincial People's Hospital (Affiliated People's Hospital) Hangzhou Medical College Hangzhou 310014 China

4. Department of Emergency Medicine Tiantai People's Hospital of Zhejiang Province (Tiantai Branch of Zhejiang Provincial People's Hospital) Hangzhou Medical College Taizhou 317200 China

5. Department of Critical Care Fudan University Shanghai Cancer Center Shanghai 200032 China

6. Department of Gastrointestinal, Colorectal and Anal Surgery Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University Hangzhou 310006 China

7. MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and Engineering Zhejiang University Hangzhou 310027 China

Abstract

AbstractOncolytic virus therapy is currently regarded as a promising approach in cancer immunotherapy. It has greater therapeutic advantages for colorectal cancer that is prone to distant metastasis. However, the therapeutic efficacy and clinical application of viral agents alone for colorectal cancer remain suboptimal. In this study, an engineered oncolytic vaccinia virus (OVV‐Luc) that expresses the firefly luciferase gene is developed and loaded Chlorin e6 (Ce6) onto the virus surface through covalent coupling, resulting in OVV‐Luc@Ce6 (OV@C). The OV@C infiltrates tumor tissue and induces endogenous luminescence through substrate catalysis, resulting in the production of reactive oxygen species. This unique system eliminates the need for an external light source, making it suitable for photodynamic therapy (PDT) in deep tissues. Moreover, this synergistic effect between PDT and viral immunotherapy enhances dendritic cell maturation, macrophage polarization, and reversal of the immunosuppressive microenvironment. This synergistic effect has the potential to convert a “cold” into a “hot” tumor, it offers valuable insights for clinical translation and application.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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