TY - JOUR
T1 - Intravesical immunotherapy with a GM-CSF armed oncolytic vesicular stomatitis virus improves outcome in bladder cancer
AU - Rangsitratkul, Coby
AU - Lawson, Christine
AU - Bernier-Godon, Francis
AU - Niavarani, Seyedeh Raheleh
AU - Boudaud, Marie
AU - Rouleau, Samuel
AU - Gladu-Corbin, Antoine Olivier
AU - Surendran, Abera
AU - Ekindi-Ndongo, Nadia
AU - Koti, Madhuri
AU - Ilkow, Carolina S.
AU - Richard, Patrick O.
AU - Tai, Lee Hwa
N1 - Funding Information:
The authors thank the patients who consented to participate in this study. The authors also thank all the institutional and federal funding support. CIHR New Investigator Award (L.T.) and FRQS Jr 1 Salary Awards (L.T., P.R.) provided salary support; Université de Sherbrooke Chair (CRMUS) in Translational Immunotherapy Research (L.T.) and CRCHUS Team Grant (L.T., P.R.) provided operating funds for this study; Université de Sherbrooke, Graduate Scholarship provided the student scholarship for C.R.
Publisher Copyright:
© 2022 The Author(s)
PY - 2022/3/17
Y1 - 2022/3/17
N2 - A significant proportion of non-muscle invasive bladder cancer cases will progress to muscle invasive disease. Transurethral resection followed by Bacillus Calmette Guerin immunotherapy can reduce this risk, while cystectomy prior to muscle invasion provides the best option for survival. Currently, there are no effective treatments for Bacillus Calmette Guerin refractory disease. A novel oncolytic vesicular stomatitis virus containing the human GM-CSF transgene (VSVd51-hGM-CSF) was rescued and tested as a potential bladder-sparing therapy for aggressive bladder cancer. The existing variant expressing mouse GM-CSF was also used. Measurement of gene expression and protein level alterations of canonical immunogenic cell death associated events on mouse and human bladder cancer cell lines and spheroids showed enhanced release of danger signals and immunogenic factors following infection with VSVd51-m/hGM-CSF. Intravesical instillation of VSVd51-mGM-CSF into MB49 bladder cancer bearing C57Bl/6 mice demonstrated enhanced activation of peripheral and bladder infiltrating effector immune cells, along with improved survival and reduced tumor volume. Importantly, virus-mediated anti-tumor immunity was recapitulated in bladder cancer patient-derived organoids. These results suggest that VSVd51-hGM-CSF is a promising viro/immunotherapy that could benefit bladder cancer patients.
AB - A significant proportion of non-muscle invasive bladder cancer cases will progress to muscle invasive disease. Transurethral resection followed by Bacillus Calmette Guerin immunotherapy can reduce this risk, while cystectomy prior to muscle invasion provides the best option for survival. Currently, there are no effective treatments for Bacillus Calmette Guerin refractory disease. A novel oncolytic vesicular stomatitis virus containing the human GM-CSF transgene (VSVd51-hGM-CSF) was rescued and tested as a potential bladder-sparing therapy for aggressive bladder cancer. The existing variant expressing mouse GM-CSF was also used. Measurement of gene expression and protein level alterations of canonical immunogenic cell death associated events on mouse and human bladder cancer cell lines and spheroids showed enhanced release of danger signals and immunogenic factors following infection with VSVd51-m/hGM-CSF. Intravesical instillation of VSVd51-mGM-CSF into MB49 bladder cancer bearing C57Bl/6 mice demonstrated enhanced activation of peripheral and bladder infiltrating effector immune cells, along with improved survival and reduced tumor volume. Importantly, virus-mediated anti-tumor immunity was recapitulated in bladder cancer patient-derived organoids. These results suggest that VSVd51-hGM-CSF is a promising viro/immunotherapy that could benefit bladder cancer patients.
KW - BCG failure
KW - GM-CSF
KW - bladder cancer
KW - bladder-sparing therapy
KW - immunogenic cell death
KW - immunotherapy
KW - oncolytic virus
KW - organoids
KW - tumor microenvironment
KW - vesicular stomatitis virus
UR - http://www.scopus.com/inward/record.url?scp=85124455857&partnerID=8YFLogxK
U2 - 10.1016/j.omto.2022.01.009
DO - 10.1016/j.omto.2022.01.009
M3 - Article
AN - SCOPUS:85124455857
SN - 2372-7705
VL - 24
SP - 507
EP - 521
JO - Molecular Therapy - Oncolytics
JF - Molecular Therapy - Oncolytics
ER -