Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytoma

Abstract DNA vaccination against cancer has become a promising strategy for inducing a specific and long-lasting antitumor immunity. However, DNA vaccines fail to generate potent immune responses when used as a single therapy. To enhance their activity into the tumor, a DNA vaccine against murine P8...

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Main Authors: Alessandra Lopes, Kevin Vanvarenberg, Špela Kos, Sophie Lucas, Didier Colau, Benoît Van den Eynde, Véronique Préat, Gaëlle Vandermeulen
Format: Article
Language:English
Published: Nature Portfolio 2018-10-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-018-33933-7
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author Alessandra Lopes
Kevin Vanvarenberg
Špela Kos
Sophie Lucas
Didier Colau
Benoît Van den Eynde
Véronique Préat
Gaëlle Vandermeulen
author_facet Alessandra Lopes
Kevin Vanvarenberg
Špela Kos
Sophie Lucas
Didier Colau
Benoît Van den Eynde
Véronique Préat
Gaëlle Vandermeulen
author_sort Alessandra Lopes
collection DOAJ
description Abstract DNA vaccination against cancer has become a promising strategy for inducing a specific and long-lasting antitumor immunity. However, DNA vaccines fail to generate potent immune responses when used as a single therapy. To enhance their activity into the tumor, a DNA vaccine against murine P815 mastocytoma was combined with antibodies directed against the immune checkpoints CTLA4 and PD1. The combination of these two strategies delayed tumor growth and enhanced specific antitumor immune cell infiltration in comparison to the corresponding single therapies. The combination also promoted IFNg, IL12 and granzyme B production in the tumor microenvironment and decreased the formation of liver metastasis in a very early phase of tumor development, enabling 90% survival. These results underline the complementarity of DNA vaccination and immune checkpoint blockers in inducing a potent immune response, by exploiting the generation of antigen-specific T cells by the vaccine and the ability of immune checkpoint blockers to enhance T cell activity and infiltration in the tumor. These findings suggest how and why a rational combination therapy can overcome the limits of DNA vaccination but could also allow responses to immune checkpoint blockers in a larger proportion of subjects.
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spelling doaj.art-8a185f7e782e4e90bd9cd7722f8cbb6c2022-12-21T23:37:46ZengNature PortfolioScientific Reports2045-23222018-10-018111110.1038/s41598-018-33933-7Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytomaAlessandra Lopes0Kevin Vanvarenberg1Špela Kos2Sophie Lucas3Didier Colau4Benoît Van den Eynde5Véronique Préat6Gaëlle Vandermeulen7Université Catholique de Louvain, Louvain Drug Research Institute, Advanced Drug Delivery and BiomaterialsUniversité Catholique de Louvain, Louvain Drug Research Institute, Advanced Drug Delivery and BiomaterialsInstitute of Oncology Ljubljana, Department of Experimental Oncologyde Duve Institute, Université Catholique de Louvainde Duve Institute, Université Catholique de Louvainde Duve Institute, Université Catholique de LouvainUniversité Catholique de Louvain, Louvain Drug Research Institute, Advanced Drug Delivery and BiomaterialsUniversité Catholique de Louvain, Louvain Drug Research Institute, Advanced Drug Delivery and BiomaterialsAbstract DNA vaccination against cancer has become a promising strategy for inducing a specific and long-lasting antitumor immunity. However, DNA vaccines fail to generate potent immune responses when used as a single therapy. To enhance their activity into the tumor, a DNA vaccine against murine P815 mastocytoma was combined with antibodies directed against the immune checkpoints CTLA4 and PD1. The combination of these two strategies delayed tumor growth and enhanced specific antitumor immune cell infiltration in comparison to the corresponding single therapies. The combination also promoted IFNg, IL12 and granzyme B production in the tumor microenvironment and decreased the formation of liver metastasis in a very early phase of tumor development, enabling 90% survival. These results underline the complementarity of DNA vaccination and immune checkpoint blockers in inducing a potent immune response, by exploiting the generation of antigen-specific T cells by the vaccine and the ability of immune checkpoint blockers to enhance T cell activity and infiltration in the tumor. These findings suggest how and why a rational combination therapy can overcome the limits of DNA vaccination but could also allow responses to immune checkpoint blockers in a larger proportion of subjects.https://doi.org/10.1038/s41598-018-33933-7P815 MastocytomaImmune Checkpoint Blockers (ICBs)Cancer VaccinationPotent Immune ResponseTumor Growth Delay
spellingShingle Alessandra Lopes
Kevin Vanvarenberg
Špela Kos
Sophie Lucas
Didier Colau
Benoît Van den Eynde
Véronique Préat
Gaëlle Vandermeulen
Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytoma
Scientific Reports
P815 Mastocytoma
Immune Checkpoint Blockers (ICBs)
Cancer Vaccination
Potent Immune Response
Tumor Growth Delay
title Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytoma
title_full Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytoma
title_fullStr Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytoma
title_full_unstemmed Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytoma
title_short Combination of immune checkpoint blockade with DNA cancer vaccine induces potent antitumor immunity against P815 mastocytoma
title_sort combination of immune checkpoint blockade with dna cancer vaccine induces potent antitumor immunity against p815 mastocytoma
topic P815 Mastocytoma
Immune Checkpoint Blockers (ICBs)
Cancer Vaccination
Potent Immune Response
Tumor Growth Delay
url https://doi.org/10.1038/s41598-018-33933-7
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