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Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy
The clinical use of anti-CD40 agonist monoclonal antibodies (mAbs) is aimed at recruiting the immune system to fight the tumor cells. This approach has been demonstrated to be effective in various preclinical models. However, human CD40 Abs displayed only modest antitumor activity in cancer patients...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326085/ https://www.ncbi.nlm.nih.gov/pubmed/35911742 http://dx.doi.org/10.3389/fimmu.2022.940674 |
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author | Salomon, Ran Dahan, Rony |
author_facet | Salomon, Ran Dahan, Rony |
author_sort | Salomon, Ran |
collection | PubMed |
description | The clinical use of anti-CD40 agonist monoclonal antibodies (mAbs) is aimed at recruiting the immune system to fight the tumor cells. This approach has been demonstrated to be effective in various preclinical models. However, human CD40 Abs displayed only modest antitumor activity in cancer patients, characterized by low efficacy and dose-limiting toxicity. While recent studies highlight the importance of engineering the Fc region of human CD40 mAbs to optimize their agonistic potency, toxicity remains the main limiting factor, restricting clinical application to suboptimal doses. Here, we discuss the current challenges in realizing the full potential of CD40 mAbs in clinical practice, and describe novel approaches designed to circumvent the systemic toxicity associated with CD40 agonism. |
format | Online Article Text |
id | pubmed-9326085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93260852022-07-28 Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy Salomon, Ran Dahan, Rony Front Immunol Immunology The clinical use of anti-CD40 agonist monoclonal antibodies (mAbs) is aimed at recruiting the immune system to fight the tumor cells. This approach has been demonstrated to be effective in various preclinical models. However, human CD40 Abs displayed only modest antitumor activity in cancer patients, characterized by low efficacy and dose-limiting toxicity. While recent studies highlight the importance of engineering the Fc region of human CD40 mAbs to optimize their agonistic potency, toxicity remains the main limiting factor, restricting clinical application to suboptimal doses. Here, we discuss the current challenges in realizing the full potential of CD40 mAbs in clinical practice, and describe novel approaches designed to circumvent the systemic toxicity associated with CD40 agonism. Frontiers Media S.A. 2022-07-13 /pmc/articles/PMC9326085/ /pubmed/35911742 http://dx.doi.org/10.3389/fimmu.2022.940674 Text en Copyright © 2022 Salomon and Dahan https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Salomon, Ran Dahan, Rony Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy |
title | Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy |
title_full | Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy |
title_fullStr | Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy |
title_full_unstemmed | Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy |
title_short | Next Generation CD40 Agonistic Antibodies for Cancer Immunotherapy |
title_sort | next generation cd40 agonistic antibodies for cancer immunotherapy |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326085/ https://www.ncbi.nlm.nih.gov/pubmed/35911742 http://dx.doi.org/10.3389/fimmu.2022.940674 |
work_keys_str_mv | AT salomonran nextgenerationcd40agonisticantibodiesforcancerimmunotherapy AT dahanrony nextgenerationcd40agonisticantibodiesforcancerimmunotherapy |