Tutorial: design, production and testing of oncolytic viruses for cancer immunotherapy.
Shashi GujarJonathan G PolVishnupriyan KManuela Lizarralde-GuerreroPrathyusha KondaGuido KroemerJohn C BellPublished in: Nature protocols (2024)
Oncolytic viruses (OVs) represent a novel class of cancer immunotherapy agents that preferentially infect and kill cancer cells and promote protective antitumor immunity. Furthermore, OVs can be used in combination with established or upcoming immunotherapeutic agents, especially immune checkpoint inhibitors, to efficiently target a wide range of malignancies. The development of OV-based therapy involves three major steps before clinical evaluation: design, production and preclinical testing. OVs can be designed as natural or engineered strains and subsequently selected for their ability to kill a broad spectrum of cancer cells rather than normal, healthy cells. OV selection is further influenced by multiple factors, such as the availability of a specific viral platform, cancer cell permissivity, the need for genetic engineering to render the virus non-pathogenic and/or more effective and logistical considerations around the use of OVs within the laboratory or clinical setting. Selected OVs are then produced and tested for their anticancer potential by using syngeneic, xenograft or humanized preclinical models wherein immunocompromised and immunocompetent setups are used to elucidate their direct oncolytic ability as well as indirect immunotherapeutic potential in vivo. Finally, OVs demonstrating the desired anticancer potential progress toward translation in patients with cancer. This tutorial provides guidelines for the design, production and preclinical testing of OVs, emphasizing considerations specific to OV technology that determine their clinical utility as cancer immunotherapy agents.
Keyphrases
- clinical evaluation
- cell therapy
- human health
- sars cov
- escherichia coli
- high throughput
- intensive care unit
- stem cells
- risk assessment
- clinical practice
- cell proliferation
- cell cycle arrest
- mesenchymal stem cells
- dna methylation
- genome wide
- monoclonal antibody
- single cell
- extracorporeal membrane oxygenation
- genetic diversity
- smoking cessation