TY - JOUR
T1 - Safety and Efficacy of an Oncolytic Adenovirus as an Immunotherapy for Canine Cancer Patients
AU - Martín-Carrasco, Clara
AU - Delgado-Bonet, Pablo
AU - Tomeo-Martín, Beatriz Davinia
AU - Pastor Milan, Josep
AU - de la Riva, Claudia
AU - Palau-Concejo, Paula
AU - Del Castillo, Noemí
AU - García-Castro, Javier
AU - Perisé-Barrios, Ana Judith
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/7/1
Y1 - 2022/7/1
N2 - The use of oncolytic viruses is an innovative approach to lyse tumor cells and induce antitumor immune responses. Eight dogs diagnosed with carcinoma/adenocarcinoma were intratumorally treated with ICOCAV15, an oncolytic canine adenovirus (CAV). To evaluate the treatment’s safety, a blood count, biochemistry, and coagulation test were performed before treatment and during follow-up. Immune populations were analyzed by flow cytometry. Anti-adenovirus antibodies were also determined. The immune infiltration, vascularization, and viral presence in the tumor were determined by CD3, CD4, CD20, CD31 and CAV by immunohistochemistry. All the dogs maintained a good quality of life during follow-up, and some had increased median survival time when compared with dogs treated with chemotherapy. No treatment-related adverse effects were detected. The Response Evaluation Criteria In Solid Tumors criteria were also assessed: two patients showed a partial response and the rest showed stable disease at various times during the study. ICOCAV15 was detected inside the tumor during follow-up, and antiviral antibodies were detected in all patients. Furthermore, the tumor-infiltrating immune cells increased after viral administration. Therefore, we suggest that intratumorally administered ICOCAV15 could represent as a new tool for the treatment of canine carcinoma because it is safe, well-tolerated by dogs, and shows promising results.
AB - The use of oncolytic viruses is an innovative approach to lyse tumor cells and induce antitumor immune responses. Eight dogs diagnosed with carcinoma/adenocarcinoma were intratumorally treated with ICOCAV15, an oncolytic canine adenovirus (CAV). To evaluate the treatment’s safety, a blood count, biochemistry, and coagulation test were performed before treatment and during follow-up. Immune populations were analyzed by flow cytometry. Anti-adenovirus antibodies were also determined. The immune infiltration, vascularization, and viral presence in the tumor were determined by CD3, CD4, CD20, CD31 and CAV by immunohistochemistry. All the dogs maintained a good quality of life during follow-up, and some had increased median survival time when compared with dogs treated with chemotherapy. No treatment-related adverse effects were detected. The Response Evaluation Criteria In Solid Tumors criteria were also assessed: two patients showed a partial response and the rest showed stable disease at various times during the study. ICOCAV15 was detected inside the tumor during follow-up, and antiviral antibodies were detected in all patients. Furthermore, the tumor-infiltrating immune cells increased after viral administration. Therefore, we suggest that intratumorally administered ICOCAV15 could represent as a new tool for the treatment of canine carcinoma because it is safe, well-tolerated by dogs, and shows promising results.
KW - ICOCAV15
KW - canine carcinoma
KW - immunotherapy
KW - oncolytic virus
KW - virotherapy
UR - https://www.scopus.com/pages/publications/85133541004
UR - https://www.mendeley.com/catalogue/18bb81ee-493c-323d-9c62-7c24841f63ce/
U2 - 10.3390/vetsci9070327
DO - 10.3390/vetsci9070327
M3 - Article
C2 - 35878344
AN - SCOPUS:85133541004
SN - 2306-7381
VL - 9
JO - Veterinary Sciences
JF - Veterinary Sciences
IS - 7
M1 - 327
ER -