Treatment of Human Glioblastoma with a Live Attenuated Zika Virus Vaccine Candidate

Author:

Chen Qi1,Wu Jin23,Ye Qing14,Ma Feng56,Zhu Qian7,Wu Yan7,Shan Chao8ORCID,Xie Xuping8ORCID,Li Dapei56,Zhan Xiaoyan2,Li Chunfeng156,Li Xiao-Feng1,Qin Xiaoling1,Zhao Tongyan1,Wu Haitao7,Shi Pei-Yong8,Man Jianghong2,Qin Cheng-Feng1ORCID

Affiliation:

1. State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, China

2. State Key Laboratory of Proteomics, National Center of Biomedical Analysis, Beijing, China

3. Tianjin Key Laboratory of Risk Assessment and Control Technology for Environment and Food Safety, Institute of Environmental Medicine, Academy of Military Medical Sciences, Tianjin, China

4. Guangzhou No.8 People's Hospital, Guangzhou Medical University, Guangzhou, China

5. Center for Systems Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China

6. Suzhou Institute of Systems Medicine, Suzhou, China

7. Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, China

8. Department of Biochemistry and Molecular Biology, Department of Pharmacology and Toxicology, Sealy Center for Structural Biology & Molecular Biophysics, University of Texas Medical Branch, Galveston, Texas, USA

Abstract

Glioblastoma (GBM), the deadliest type of brain tumor, is currently incurable because of its high recurrence rate after traditional treatments, including surgery to remove the main part of the tumor and radiation and chemotherapy to target residual tumor cells. These treatments fail mainly due to the presence of a cell subpopulation called glioma stem cells (GSCs), which are resistant to radiation and chemotherapy and capable of self-renewal and tumorigenicity. Because Zika virus (ZIKV) has an oncolytic tropism for infecting GSCs, we tested a live attenuated ZIKV vaccine candidate (ZIKV-LAV) for the treatment of human GBM in a human GSC-derived orthotopic model. Our results showed that ZIKV-LAV retained good efficacy against glioblastoma by selectively killing GSCs within the tumor. In addition, ZIKV-LAV exhibited an excellent safety profile upon intracerebral injection into the treated animals. The good balance between the safety of ZIKV-LAV and its efficacy against human GSCs suggests that it is a potential candidate for combination with the current treatment regimen for GBM therapy.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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