Erythrocyte‐Leveraged Oncolytic Virotherapy (ELeOVt): Oncolytic Virus Assembly on Erythrocyte Surface to Combat Pulmonary Metastasis and Alleviate Side Effects

Author:

Liu Mingyang123,Zhang Ruizhe123,Huang Hanwei123,Liu Pengfei13,Zhao Xu123,Wu Hu123,He Ying2,Xu Ruizhe2,Qin Xifeng2,Cheng Zhenguo4,Liu Hongyu13,Ergonul Onder5,Can Füsun5,Ouyang Defang6,Wang Zhenning13,Pang Zhiqing2ORCID,Liu Funan137ORCID

Affiliation:

1. Department of Surgical Oncology and General Surgery The First Hospital of China Medical University 155 North Nanjing Street, Heping District Shenyang 110001 China

2. Department of Pharmaceutics School of Pharmacy Fudan University and Key Laboratory of Smart Drug Delivery Ministry of Education Shanghai 201203 China

3. Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors China Medical University Ministry of Education 155 North Nanjing Street, Heping District Shenyang 110001 China

4. Sino‐British Research Centre for Molecular Oncology National Centre for International Research in Cell and Gene Therapy School of Basic Medical Sciences Academy of Medical Sciences Zhengzhou University Zhengzhou 450052 China

5. Koç University Iş Bank Center for Infectious Diseases (KUISCID) Koç University School of Medicine and American Hospital Istanbul 34010 Turkey

6. State Key Laboratory of Quality Research in Chinese Medicine Institute of Chinese Medical Sciences (ICMS) University of Macau Macau 999078 China

7. Phase I Clinical Trials Center The First Hospital China Medical University 518 North Chuangxin Road, Baita Street, Hunnan District Shenyang Liaoning 110102 China

Abstract

AbstractDespite being a new promising tool for cancer therapy, intravenous delivery of oncolytic viruses (OVs) is greatly limited by poor tumor targeting, rapid clearance in the blood, severe organ toxicity, and cytokine release syndrome. Herein, a simple and efficient strategy of erythrocyte‐leveraged oncolytic virotherapy (ELeOVt) is reported, which for the first time assembled OVs on the surface of erythrocytes with up to near 100% efficiency and allowed targeted delivery of OVs to the lung after intravenous injection to achieve excellent treatment of pulmonary metastases while greatly improving the biocompatibility of OVs as a drug. Polyethyleneimine (PEI) as a bridge to assemble OVs on erythrocytes also played an important role in promoting the transfection of OVs. It is found that ELeOVt approach significantly prolonged the circulation time of OVs and increased the OVs distribution in the lung by more than tenfold, thereby significantly improving the treatment of lung metastases while reducing organ and systemic toxicity. Taken together, these findings suggest that the ELeOVt provides a biocompatible, efficient, and widely available approach to empower OVs to combat lung metastasis.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Liaoning Revitalization Talents Program

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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