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Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity

The recruitment of antibody naturally present in human blood stream at the surface of cancer cells have been proved a promising immunotherapeutic strategy to fight cancer. Antibody recruiting molecules (ARMs) combining tumor and antibody binding modules have been developed for this purpose, however...

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Detalles Bibliográficos
Autores principales: Goyard, David, Diriwari, Peremobowei Iyanu, Berthet, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792828/
https://www.ncbi.nlm.nih.gov/pubmed/35211675
http://dx.doi.org/10.1039/d1md00262g
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author Goyard, David
Diriwari, Peremobowei Iyanu
Berthet, Nathalie
author_facet Goyard, David
Diriwari, Peremobowei Iyanu
Berthet, Nathalie
author_sort Goyard, David
collection PubMed
description The recruitment of antibody naturally present in human blood stream at the surface of cancer cells have been proved a promising immunotherapeutic strategy to fight cancer. Antibody recruiting molecules (ARMs) combining tumor and antibody binding modules have been developed for this purpose, however the formation of the interacting complex with both antibody and cell is difficult to optimize to stimulate immune-mediated cytotoxicity. To circumvent this limitation, we report herein a more direct approach combining cell metabolism of azido-sugar and bio-orthogonal click chemistry to conjugate at the cell glycocalyx structurally well-defined glycodendrimers as antibody binding module (ABM). We demonstrate that this strategy allows not only the recruitment of natural antibody at the surface of isolated cells or solid tumor models but also activate a cytotoxic response with human serum as unique source of immune effectors.
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spelling pubmed-87928282022-02-23 Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity Goyard, David Diriwari, Peremobowei Iyanu Berthet, Nathalie RSC Med Chem Chemistry The recruitment of antibody naturally present in human blood stream at the surface of cancer cells have been proved a promising immunotherapeutic strategy to fight cancer. Antibody recruiting molecules (ARMs) combining tumor and antibody binding modules have been developed for this purpose, however the formation of the interacting complex with both antibody and cell is difficult to optimize to stimulate immune-mediated cytotoxicity. To circumvent this limitation, we report herein a more direct approach combining cell metabolism of azido-sugar and bio-orthogonal click chemistry to conjugate at the cell glycocalyx structurally well-defined glycodendrimers as antibody binding module (ABM). We demonstrate that this strategy allows not only the recruitment of natural antibody at the surface of isolated cells or solid tumor models but also activate a cytotoxic response with human serum as unique source of immune effectors. RSC 2021-11-09 /pmc/articles/PMC8792828/ /pubmed/35211675 http://dx.doi.org/10.1039/d1md00262g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Goyard, David
Diriwari, Peremobowei Iyanu
Berthet, Nathalie
Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity
title Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity
title_full Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity
title_fullStr Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity
title_full_unstemmed Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity
title_short Metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity
title_sort metabolic labelling of cancer cells with glycodendrimers stimulate immune-mediated cytotoxicity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792828/
https://www.ncbi.nlm.nih.gov/pubmed/35211675
http://dx.doi.org/10.1039/d1md00262g
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