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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...

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Detalles Bibliográficos
Autores principales: Salomon, Ran, Dahan, Rony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
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.
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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
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