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Genetic modification of oncolytic viruses to enhance antitumor immunity.
Davola, Maria Eugenia; Vito, Alyssa; Wei, Jiarun; El-Sayes, Nader; Workenhe, Samuel; Mossman, Karen Louise.
Affiliation
  • Davola ME; Department of Pathology and Molecular Medicine, McMaster Immunology Research Centre, Michael DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
  • Vito A; Department of Biochemistry and Biomedical Science, McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada.
  • Wei J; Department of Biochemistry and Biomedical Science, McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada.
  • El-Sayes N; Department of Biochemistry and Biomedical Science, McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada.
  • Workenhe S; Department of Pathology and Molecular Medicine, McMaster Immunology Research Centre, Michael DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
  • Mossman KL; Department of Pathology and Molecular Medicine, McMaster Immunology Research Centre, Michael DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada. Electronic address: mossk@mcmaster.ca.
Methods Enzymol ; 635: 231-250, 2020.
Article in En | MEDLINE | ID: mdl-32122548
ABSTRACT
Among the many immunotherapies being developed and tested both preclinically and clinically, oncolytic viruses (OVs) are gaining traction as a forerunner in the search for potent new therapeutic agents, with a genetically engineered herpes simplex virus type 1 (HSV-1) recently approved by the FDA for the treatment of melanoma. The great potential of OVs to fight cancer is driving different approaches to improve OV-based therapy, with genetic modification of OVs to enhance host antitumor immunity being one of the most promising approaches. In this chapter we describe possible modifications in the OV genome that could increase its antitumor activity and immunostimulatory capacity, together with different methods to achieve these goals. Finally, we present different analyses to verify the desired genetic modification and evaluate its impact on host antitumor immunity in preliminary stages.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oncolytic Viruses / Oncolytic Virotherapy / Neoplasms Limits: Humans Language: En Journal: Methods Enzymol Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oncolytic Viruses / Oncolytic Virotherapy / Neoplasms Limits: Humans Language: En Journal: Methods Enzymol Year: 2020 Document type: Article Affiliation country: