Synergistic antitumor response with recombinant modified virus Ankara armed with CD40L and CD137L against peritoneal carcinomatosis

Recombinant-modified vaccinia virus Ankara (rMVA) is known to elicit potent antitumor immune responses in preclinical models due to its inherent ability to activate the innate immune system and the activation of adaptive responses mediated by the expression of tumor antigens and costimulus-providing...

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Autores: Bella-Carreño, Á. (Ángela)|||/items/0c095363-d839-41ea-aaa1-258956fba96c, Arrizabalaga-Astigarraga, L. (Leire)|||/items/651c6b4c-6c43-4d26-9301-b7a37c43828c, Di-Trani, C.A. (Claudia Augusta)|||/items/5d899126-779d-4c97-8232-95bfe18f9f26, Cirella, A. (Assunta)|||/items/398b3896-8ce3-4831-8ebc-1d86487cd790, Fernández-Sendín, M. (Myriam)|||/items/d32b0470-d2c8-459d-9920-c80a0f4671fe, Gomar, C. (Celia)|||/items/a228ce92-d4fa-45e7-b0d2-d58e77b8f4b7, Russo-Cabrera, J. S. (Joan Salvador)|||/items/0d4ea06f-1c94-41c6-b183-0af79d9eab7f, Rodriguez, I. (Inmaculada)|||/items/1de605b4-b2b9-4754-8a45-990e5e3895dd, González-Gomariza, J. (José)|||/items/a519f7ad-9cc9-4476-b22f-bfc0c46683d8, Álvarez, M. (Maite)|||/items/869c2b2f-e806-47ac-8d76-303de908d205, Teijeira-Sánchez, A. (Álvaro)|||/items/8a954ec4-8458-46ea-b8e6-3165119bef30, Medina-Echeverz, J. (José)|||/items/269636db-a0ed-439d-a24f-1096e6ed985d, Hinterberger, M. (Maria)|||/items/fe82f793-dad9-4fca-8afa-0d7e6c360bb6, Hochrein, H. (Hubertus)|||/items/98609255-ce5a-4cf0-b8a3-1ea556e6b6fd, Melero, I. (Ignacio)|||/items/82113ea8-7ce1-49d5-9ee3-42cf20db1c4e, Berraondo-López, P. (Pedro)|||/items/b1f8ccc3-8e08-4ece-967c-64ccfc0e5b91, Aranda-Vega, F. (Fernando)|||/items/967c4675-0318-4d3c-97dc-b5b09026995f
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/116717
Acceso en línea:https://hdl.handle.net/10171/116717
Access Level:acceso abierto
Palabra clave:CD137L
CD40L
CD8 immune response
Peritoneal carcinomatosis
Cancer immunotherapy
Descripción
Sumario:Recombinant-modified vaccinia virus Ankara (rMVA) is known to elicit potent antitumor immune responses in preclinical models due to its inherent ability to activate the innate immune system and the activation of adaptive responses mediated by the expression of tumor antigens and costimulus-providing molecules, such as CD40L and CD137L. Here, we evaluated different rMVA vectors in preclinical peritoneal carcinomatosis models (ID8.OVA-Vegf/GFP and MC38). We compared rMVA vectors expressing a tumor antigen (OVA or gp70) either alone or co-expressed with CD40L or/and CD137L. In tumor-free mice, the vector coding for the triple combination was only slightly superior, whereas, in tumor-bearing animals, we observed a synergistic induction of T lymphocytes specific against vector-encoded and non-encoded tumor-associated antigens. The enhanced activation of the immune response was associated with improved survival in mice with peritoneal carcinomatosis treated with a rMVA vector encoding both CD40L and CD137L. Thus, the triple transgene combination in vaccinia viral vectors represents a promising strategy for the treatment of peritoneal carcinomatosis.