Your browser doesn't support javascript.
loading
Intracellular delivery of oncolytic viruses with engineered Salmonella causes viral replication and cell death.
Khanduja, Shradha; Bloom, Shoshana M K; Raman, Vishnu; Deshpande, Chinmay P; Hall, Christopher L; Forbes, Neil S.
Afiliação
  • Khanduja S; Department of Chemical Engineering, University of Massachusetts, Amherst, Amherst, MA, USA.
  • Bloom SMK; Department of Chemical Engineering, University of Massachusetts, Amherst, Amherst, MA, USA.
  • Raman V; Department of Chemical Engineering, University of Massachusetts, Amherst, Amherst, MA, USA.
  • Deshpande CP; Department of Chemical Engineering, University of Massachusetts, Amherst, Amherst, MA, USA.
  • Hall CL; Department of Chemical Engineering, University of Massachusetts, Amherst, Amherst, MA, USA.
  • Forbes NS; Department of Chemical Engineering, University of Massachusetts, Amherst, Amherst, MA, USA.
iScience ; 27(6): 109813, 2024 Jun 21.
Article em En | MEDLINE | ID: mdl-38799578
ABSTRACT
As therapies, oncolytic viruses regress tumors and have the potential to induce antitumor immune responses that clear hard-to-treat and late-stage cancers. Despite this promise, clearance from the blood prevents treatment of internal solid tumors. To address this issue, we developed virus-delivering Salmonella (VDS) to carry oncolytic viruses into cancer cells. The VDS strain contains the PsseJ-lysE delivery circuit and has deletions in four homologous recombination genes (ΔrecB, ΔsbcB, ΔsbcCD, and ΔrecF) to preserve essential hairpins in the viral genome required for replication and infectivity. VDS delivered the genome for minute virus of mice (MVMp) to multiple cancers, including breast, pancreatic, and osteosarcoma. Viral delivery produced functional viral particles that are cytotoxic and infective to neighboring cells. The release of mature virions initiated new rounds of infection and amplified the infection. Using Salmonella for delivery will circumvent the limitations of oncolytic viruses and will provide a new therapy for many cancers.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA