Oncolytic Maraba Virus MG1 as a Treatment for Sarcoma. Issue 6 (21st June 2017)
- Record Type:
- Journal Article
- Title:
- Oncolytic Maraba Virus MG1 as a Treatment for Sarcoma. Issue 6 (21st June 2017)
- Main Title:
- Oncolytic Maraba Virus MG1 as a Treatment for Sarcoma
- Authors:
- Le Boeuf, Fabrice
Selman, Mohammed
Son, Hwan Hee
Bergeron, Anabel
Chen, Andrew
Tsang, Jovian
Butterwick, Derek
Arulanandam, Rozanne
Forbes, Nicole E.
Tzelepis, Fanny
Bell, John C.
Werier, Joel
Abdelbary, Hesham
Diallo, Jean‐Simon - Abstract:
- Abstract : The poor prognosis of patients with advanced bone and soft‐tissue sarcoma has not changed in the past several decades, highlighting the necessity for new therapeutic approaches. Immunotherapies, including oncolytic viral (OV) therapy, have shown great promise in a number of clinical trials for a variety of tumor types. However, the effective application of OV in treating sarcoma still remains to be demonstrated. Although few pre‐clinical studies using distinct OVs have been performed and demonstrated therapeutic benefit in sarcoma models, a side‐by‐side comparison of clinically relevant OV platforms has not been performed. Four clinically relevant OV platforms (Reovirus, Vaccinia virus, Herpes‐simplex virus and Rhabdovirus) were screened for their ability to infect and kill human and canine sarcoma cell lines in vitro, and human sarcoma specimens ex vivo . In vivo treatment efficacy was tested in a murine model. The rhabdovirus MG1 demonstrated the highest potency in vitro . Ex vivo, MG1 productively infected more than 80% of human sarcoma tissues tested, and treatment in vivo led to a significant increase in long‐lasting cures in sarcoma‐bearing mice. Importantly, MG1 treatment induced the generation of memory immune response that provided protection against a subsequent tumor challenge. This study opens the door for the use of MG1‐based oncolytic immunotherapy strategies as treatment for sarcoma or as a component of a combined therapy. Abstract : What's new? TheAbstract : The poor prognosis of patients with advanced bone and soft‐tissue sarcoma has not changed in the past several decades, highlighting the necessity for new therapeutic approaches. Immunotherapies, including oncolytic viral (OV) therapy, have shown great promise in a number of clinical trials for a variety of tumor types. However, the effective application of OV in treating sarcoma still remains to be demonstrated. Although few pre‐clinical studies using distinct OVs have been performed and demonstrated therapeutic benefit in sarcoma models, a side‐by‐side comparison of clinically relevant OV platforms has not been performed. Four clinically relevant OV platforms (Reovirus, Vaccinia virus, Herpes‐simplex virus and Rhabdovirus) were screened for their ability to infect and kill human and canine sarcoma cell lines in vitro, and human sarcoma specimens ex vivo . In vivo treatment efficacy was tested in a murine model. The rhabdovirus MG1 demonstrated the highest potency in vitro . Ex vivo, MG1 productively infected more than 80% of human sarcoma tissues tested, and treatment in vivo led to a significant increase in long‐lasting cures in sarcoma‐bearing mice. Importantly, MG1 treatment induced the generation of memory immune response that provided protection against a subsequent tumor challenge. This study opens the door for the use of MG1‐based oncolytic immunotherapy strategies as treatment for sarcoma or as a component of a combined therapy. Abstract : What's new? The prognosis for advanced sarcoma remains poor, and new approaches to treatment are urgently needed. In this study of various oncolytic viral (OV) therapies, the authors found that a rhabdovirus called MG1 produced the most promising response in mice. In addition, MG1 treatment induced the generation of a memory immune response that provided protection against a subsequent tumor challenge. These results suggest that MG1‐based oncolytic immunotherapy may offer a promising treatment strategy for sarcoma, either alone or as a component of a combined therapy. … (more)
- Is Part Of:
- International journal of cancer. Volume 141:Issue 6(2017:Sep. 15)
- Journal:
- International journal of cancer
- Issue:
- Volume 141:Issue 6(2017:Sep. 15)
- Issue Display:
- Volume 141, Issue 6 (2017)
- Year:
- 2017
- Volume:
- 141
- Issue:
- 6
- Issue Sort Value:
- 2017-0141-0006-0000
- Page Start:
- 1257
- Page End:
- 1264
- Publication Date:
- 2017-06-21
- Subjects:
- Cancer -- Periodicals
Cancer -- Prevention -- Periodicals
616.994 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0215 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ijc.30813 ↗
- Languages:
- English
- ISSNs:
- 0020-7136
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.156000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2833.xml