Development of Group B Coxsackievirus as an Oncolytic Virus: Opportunities and Challenges

被引:25
作者
Liu, Huitao [1 ,2 ]
Luo, Honglin [1 ,3 ]
机构
[1] Univ British Columbia, St Pauls Hosp, Ctr Heart Lung Innovat, Vancouver, BC V6Z 1Y6, Canada
[2] Univ British Columbia, Dept Expt Med, Vancouver, BC V6Z 1Y6, Canada
[3] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6Z 1Y6, Canada
来源
VIRUSES-BASEL | 2021年 / 13卷 / 06期
关键词
coxsackievirus B; oncolytic virus; cancer; virotherapy; toxicity; anti-tumor immunity; CAR-T-CELLS; ADENOVIRUS RECEPTOR; PD-1/PD-L1; BLOCKADE; MOLECULAR-BASIS; IMMUNE EVASION; GENE-THERAPY; REPLICATION; DELIVERY; STRAIN; VIROTHERAPY;
D O I
10.3390/v13061082
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Oncolytic viruses have emerged as a promising strategy for cancer therapy due to their dual ability to selectively infect and lyse tumor cells and to induce systemic anti-tumor immunity. Among various candidate viruses, coxsackievirus group B (CVBs) have attracted increasing attention in recent years. CVBs are a group of small, non-enveloped, single-stranded, positive-sense RNA viruses, belonging to species human Enterovirus B in the genus Enterovirus of the family Picornaviridae. Preclinical studies have demonstrated potent anti-tumor activities for CVBs, particularly type 3, against multiple cancer types, including lung, breast, and colorectal cancer. Various approaches have been proposed or applied to enhance the safety and specificity of CVBs towards tumor cells and to further increase their anti-tumor efficacy. This review summarizes current knowledge and strategies for developing CVBs as oncolytic viruses for cancer virotherapy. The challenges arising from these studies and future prospects are also discussed in this review.
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页数:15
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