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Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth

The transmembrane adaptor phosphoprotein associated with glycosphingolipid-enriched microdomains 1 (PAG) is phosphorylated in T cells downstream of PD-1 signaling and contributes to the resulting functional inhibition of multiple cellular processes. Furthermore, PAG expression is negatively correlat...

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Autores principales: Strazza, Marianne, Moore, Emily K., Adam, Kieran, Azoulay-Alfaguter, Inbar, Mor, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664140/
https://www.ncbi.nlm.nih.gov/pubmed/36419471
http://dx.doi.org/10.1016/j.omtm.2022.10.012
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author Strazza, Marianne
Moore, Emily K.
Adam, Kieran
Azoulay-Alfaguter, Inbar
Mor, Adam
author_facet Strazza, Marianne
Moore, Emily K.
Adam, Kieran
Azoulay-Alfaguter, Inbar
Mor, Adam
author_sort Strazza, Marianne
collection PubMed
description The transmembrane adaptor phosphoprotein associated with glycosphingolipid-enriched microdomains 1 (PAG) is phosphorylated in T cells downstream of PD-1 signaling and contributes to the resulting functional inhibition of multiple cellular processes. Furthermore, PAG expression is negatively correlated with survival in multiple human tumors and is a driver of murine tumor growth and immune evasion. Here we develop an antibody that targets the extracellular domain of human PAG, with cross-reactivity to murine PAG. We demonstrate that this antibody binds to extracellular PAG on intact cells and affects T cell activation. Finally, we show that administration of anti-PAG monoclonal antibody in combination with anti-PD-1 antibody to mice bearing MC38 tumors limited tumor growth and enhanced T cell infiltration to tumors.
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spelling pubmed-96641402022-11-22 Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth Strazza, Marianne Moore, Emily K. Adam, Kieran Azoulay-Alfaguter, Inbar Mor, Adam Mol Ther Methods Clin Dev Original Article The transmembrane adaptor phosphoprotein associated with glycosphingolipid-enriched microdomains 1 (PAG) is phosphorylated in T cells downstream of PD-1 signaling and contributes to the resulting functional inhibition of multiple cellular processes. Furthermore, PAG expression is negatively correlated with survival in multiple human tumors and is a driver of murine tumor growth and immune evasion. Here we develop an antibody that targets the extracellular domain of human PAG, with cross-reactivity to murine PAG. We demonstrate that this antibody binds to extracellular PAG on intact cells and affects T cell activation. Finally, we show that administration of anti-PAG monoclonal antibody in combination with anti-PD-1 antibody to mice bearing MC38 tumors limited tumor growth and enhanced T cell infiltration to tumors. American Society of Gene & Cell Therapy 2022-11-09 /pmc/articles/PMC9664140/ /pubmed/36419471 http://dx.doi.org/10.1016/j.omtm.2022.10.012 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Strazza, Marianne
Moore, Emily K.
Adam, Kieran
Azoulay-Alfaguter, Inbar
Mor, Adam
Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth
title Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth
title_full Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth
title_fullStr Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth
title_full_unstemmed Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth
title_short Neutralization of the adaptor protein PAG by monoclonal antibody limits murine tumor growth
title_sort neutralization of the adaptor protein pag by monoclonal antibody limits murine tumor growth
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664140/
https://www.ncbi.nlm.nih.gov/pubmed/36419471
http://dx.doi.org/10.1016/j.omtm.2022.10.012
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