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Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion
BACKGROUND: A number of different immune pathways are involved in the effective killing of cancer cells, collectively named as the ‘Cancer Immunity Cycle’. Anti-PD-1 checkpoint blockade (CPB) therapy is active on one of these pathways and reinvigorates anticancer T cell immunity, leading to long-ter...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627409/ https://www.ncbi.nlm.nih.gov/pubmed/34824160 http://dx.doi.org/10.1136/jitc-2021-003480 |
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author | D'Alise, Anna Morena Leoni, Guido De Lucia, Maria Langone, Francesca Nocchi, Linda Tucci, Fabio Giovanni Micarelli, Elisa Cotugno, Gabriella Troise, Fulvia Garzia, Irene Vitale, Rosa Bignone, Veronica Di Matteo, Elena Bartolomeo, Rosa Charych, Deborah H Lahm, Armin Zalevsky, Jonathan Nicosia, Alfredo Scarselli, Elisa |
author_facet | D'Alise, Anna Morena Leoni, Guido De Lucia, Maria Langone, Francesca Nocchi, Linda Tucci, Fabio Giovanni Micarelli, Elisa Cotugno, Gabriella Troise, Fulvia Garzia, Irene Vitale, Rosa Bignone, Veronica Di Matteo, Elena Bartolomeo, Rosa Charych, Deborah H Lahm, Armin Zalevsky, Jonathan Nicosia, Alfredo Scarselli, Elisa |
author_sort | D'Alise, Anna Morena |
collection | PubMed |
description | BACKGROUND: A number of different immune pathways are involved in the effective killing of cancer cells, collectively named as the ‘Cancer Immunity Cycle’. Anti-PD-1 checkpoint blockade (CPB) therapy is active on one of these pathways and reinvigorates anticancer T cell immunity, leading to long-term responses in a limited fraction of patients with cancer. We have previously shown that neoantigens-based adenovirus vectored vaccine in combination with anti-PD-1 further expands pre-existing anticancer immunity and elicits novel neoantigen-specific T cells thereby increasing efficacy to 50% of tumor clearance in mice. Here we added a third component to the CPB plus vaccine combination, which is able to modify the suppressive tumor microenvironment by reducing the number of tumor-infiltrating regulatory T cells (Tregs), as strategy for improving the therapeutic efficacy and overcoming resistance. METHODS: The antitumor efficacy of anti-PD-1, neoantigen vaccine and Treg modulating agents, either Bempegaldesleukin (BEMPEG: NKTR-214) or an anti-CTLA-4 mAb with Treg-depleting activity, was investigated in murine tumor models. We evaluated tumor growth in treated animals, neoantigen-specific T cells in tumors, tumor-infiltrating lymphocytes (TILs) and intratumoral Tregs. RESULTS: The addition of BEMPEG or anti-CTLA-4 to the combination of vaccine and anti-PD-1 led to complete eradication of large tumors in nearby 100% of treated animals, in association with expansion and activation of cancer neoantigen-specific T cells and reduction of tumor-infiltrating Tregs. CONCLUSION: These data support the notion that the integrated regulation of three steps of the cancer immunity cycle, including expansion of neoantigen-specific T cells, reversal of the exhausted T cell phenotype together with the reduction of intratumoral Tregs may represent a novel rationally designed drug combination approach to achieve higher cure rates. |
format | Online Article Text |
id | pubmed-8627409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-86274092021-12-10 Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion D'Alise, Anna Morena Leoni, Guido De Lucia, Maria Langone, Francesca Nocchi, Linda Tucci, Fabio Giovanni Micarelli, Elisa Cotugno, Gabriella Troise, Fulvia Garzia, Irene Vitale, Rosa Bignone, Veronica Di Matteo, Elena Bartolomeo, Rosa Charych, Deborah H Lahm, Armin Zalevsky, Jonathan Nicosia, Alfredo Scarselli, Elisa J Immunother Cancer Basic Tumor Immunology BACKGROUND: A number of different immune pathways are involved in the effective killing of cancer cells, collectively named as the ‘Cancer Immunity Cycle’. Anti-PD-1 checkpoint blockade (CPB) therapy is active on one of these pathways and reinvigorates anticancer T cell immunity, leading to long-term responses in a limited fraction of patients with cancer. We have previously shown that neoantigens-based adenovirus vectored vaccine in combination with anti-PD-1 further expands pre-existing anticancer immunity and elicits novel neoantigen-specific T cells thereby increasing efficacy to 50% of tumor clearance in mice. Here we added a third component to the CPB plus vaccine combination, which is able to modify the suppressive tumor microenvironment by reducing the number of tumor-infiltrating regulatory T cells (Tregs), as strategy for improving the therapeutic efficacy and overcoming resistance. METHODS: The antitumor efficacy of anti-PD-1, neoantigen vaccine and Treg modulating agents, either Bempegaldesleukin (BEMPEG: NKTR-214) or an anti-CTLA-4 mAb with Treg-depleting activity, was investigated in murine tumor models. We evaluated tumor growth in treated animals, neoantigen-specific T cells in tumors, tumor-infiltrating lymphocytes (TILs) and intratumoral Tregs. RESULTS: The addition of BEMPEG or anti-CTLA-4 to the combination of vaccine and anti-PD-1 led to complete eradication of large tumors in nearby 100% of treated animals, in association with expansion and activation of cancer neoantigen-specific T cells and reduction of tumor-infiltrating Tregs. CONCLUSION: These data support the notion that the integrated regulation of three steps of the cancer immunity cycle, including expansion of neoantigen-specific T cells, reversal of the exhausted T cell phenotype together with the reduction of intratumoral Tregs may represent a novel rationally designed drug combination approach to achieve higher cure rates. BMJ Publishing Group 2021-11-25 /pmc/articles/PMC8627409/ /pubmed/34824160 http://dx.doi.org/10.1136/jitc-2021-003480 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Basic Tumor Immunology D'Alise, Anna Morena Leoni, Guido De Lucia, Maria Langone, Francesca Nocchi, Linda Tucci, Fabio Giovanni Micarelli, Elisa Cotugno, Gabriella Troise, Fulvia Garzia, Irene Vitale, Rosa Bignone, Veronica Di Matteo, Elena Bartolomeo, Rosa Charych, Deborah H Lahm, Armin Zalevsky, Jonathan Nicosia, Alfredo Scarselli, Elisa Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion |
title | Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion |
title_full | Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion |
title_fullStr | Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion |
title_full_unstemmed | Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion |
title_short | Maximizing cancer therapy via complementary mechanisms of immune activation: PD-1 blockade, neoantigen vaccination, and Tregs depletion |
title_sort | maximizing cancer therapy via complementary mechanisms of immune activation: pd-1 blockade, neoantigen vaccination, and tregs depletion |
topic | Basic Tumor Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627409/ https://www.ncbi.nlm.nih.gov/pubmed/34824160 http://dx.doi.org/10.1136/jitc-2021-003480 |
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