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Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking
Antibody agonists targeting tumor necrosis factor (TNF) superfamily receptors, including CD40, are being tested therapeutically as anticancer agents. Studies in mice have shown that anti-CD40 monoclonal antibody (mAb) requires Fc-receptor (FcR) engagement to activate antitumor immunity. In contrast,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091558/ https://www.ncbi.nlm.nih.gov/pubmed/25097801 http://dx.doi.org/10.4161/onci.28610 |
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author | Richman, Lee P Vonderheide, Robert H |
author_facet | Richman, Lee P Vonderheide, Robert H |
author_sort | Richman, Lee P |
collection | PubMed |
description | Antibody agonists targeting tumor necrosis factor (TNF) superfamily receptors, including CD40, are being tested therapeutically as anticancer agents. Studies in mice have shown that anti-CD40 monoclonal antibody (mAb) requires Fc-receptor (FcR) engagement to activate antitumor immunity. In contrast, we have reported that clinically active anti-human CD40 mAb CP-870,893 does not require FcR crosslinking, a finding with translational implications. |
format | Online Article Text |
id | pubmed-4091558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-40915582014-08-05 Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking Richman, Lee P Vonderheide, Robert H Oncoimmunology Author's View Antibody agonists targeting tumor necrosis factor (TNF) superfamily receptors, including CD40, are being tested therapeutically as anticancer agents. Studies in mice have shown that anti-CD40 monoclonal antibody (mAb) requires Fc-receptor (FcR) engagement to activate antitumor immunity. In contrast, we have reported that clinically active anti-human CD40 mAb CP-870,893 does not require FcR crosslinking, a finding with translational implications. Landes Bioscience 2014-04-29 /pmc/articles/PMC4091558/ /pubmed/25097801 http://dx.doi.org/10.4161/onci.28610 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Author's View Richman, Lee P Vonderheide, Robert H Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking |
title | Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking |
title_full | Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking |
title_fullStr | Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking |
title_full_unstemmed | Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking |
title_short | Anti-human CD40 monoclonal antibody therapy is potent without FcR crosslinking |
title_sort | anti-human cd40 monoclonal antibody therapy is potent without fcr crosslinking |
topic | Author's View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091558/ https://www.ncbi.nlm.nih.gov/pubmed/25097801 http://dx.doi.org/10.4161/onci.28610 |
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