Abstract
Background
Vaccinia virus was widely used in the World Health Organization’s smallpox eradication campaign and is currently a promising vector for gene therapy owing to its unique characteristics. Vaccinia virus can selectively replicate and propagate productively in tumor cells, resulting in oncolysis. In addition, rapid viral particle production, wide host range, large genome size (approximately 200 kb), and safe handling render vaccinia virus a suitable vector for gene therapy.
Materials and methods
Cancer vaccines and gene therapy are being studied in clinical trials and experiment researches. However, we put forward unique challenges of optimal selection of foreign genes, administration and modification of VACV, personalized medicine, and other existing problems, based on current researches and our own experiments.
Conclusion
This review presents an overview of the vaccinia virus from its mechanisms to medical researches and clinical trials. We believe that the solution to these problems will contribute to understanding mechanisms of VACV and provide a theoretical basis for clinical treatment.
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Abbreviations
- VACV:
-
Vaccinia virus
- WR:
-
Western reserve
- VTT:
-
Vaccinia virus Tian Tan strain
- TK:
-
Thymidine tyrosine kinase
- GM–CSF:
-
Granulocyte–macrophage colony stimulating factor
- MVA:
-
Modified vaccinia Ankara
- CD:
-
Cytosinedeaminase
- 5-FU:
-
5-fluorouracil
- RNAi:
-
RNA interference
- siRNA:
-
Short interfering double-stranded RNA
- shRNA:
-
Short hairpin RNA
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Acknowledgements
We thanked Jie Liu for the literature search.
Funding
This study was supported by National Natural Science Foundation of China (81703061).
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XY and BH did the data analysis and interpretation, and manuscript writing; LD did collection and assembly of data; ZH did the conception/design, provision of study material or patients, and final approval of manuscript.
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Yang, X., Huang, B., Deng, L. et al. Progress in gene therapy using oncolytic vaccinia virus as vectors. J Cancer Res Clin Oncol 144, 2433–2440 (2018). https://doi.org/10.1007/s00432-018-2762-x
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DOI: https://doi.org/10.1007/s00432-018-2762-x