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Tutorial: design, production and testing of oncolytic viruses for cancer immunotherapy.
Gujar, Shashi; Pol, Jonathan G; Kumar, Vishnupriyan; Lizarralde-Guerrero, Manuela; Konda, Prathyusha; Kroemer, Guido; Bell, John C.
Afiliação
  • Gujar S; Department of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Pol JG; Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Kumar V; Department of Biology, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Lizarralde-Guerrero M; Beatrice Hunter Cancer Research Institute, Halifax, Nova Scotia, Canada.
  • Konda P; INSERM, U1138, Paris, France.
  • Kroemer G; Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, Paris, France.
  • Bell JC; Université Paris Cité, Paris, France.
Nat Protoc ; 2024 May 20.
Article em En | MEDLINE | ID: mdl-38769145
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Protoc Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Protoc Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá