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Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells
We have developed a fully synthetic and multifunctional antibody‐recruiting molecule (ARM) to guide natural antibodies already present in the blood stream against cancer cells without pre‐immunization. Our ARM is composed of antibody and tumor binding modules (i.e., ABM and TBM) displaying clustered...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916168/ https://www.ncbi.nlm.nih.gov/pubmed/31613028 http://dx.doi.org/10.1002/chem.201903327 |
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author | Liet, Benjamin Laigre, Eugénie Goyard, David Todaro, Biagio Tiertant, Claire Boturyn, Didier Berthet, Nathalie Renaudet, Olivier |
author_facet | Liet, Benjamin Laigre, Eugénie Goyard, David Todaro, Biagio Tiertant, Claire Boturyn, Didier Berthet, Nathalie Renaudet, Olivier |
author_sort | Liet, Benjamin |
collection | PubMed |
description | We have developed a fully synthetic and multifunctional antibody‐recruiting molecule (ARM) to guide natural antibodies already present in the blood stream against cancer cells without pre‐immunization. Our ARM is composed of antibody and tumor binding modules (i.e., ABM and TBM) displaying clustered rhamnose and cyclo‐RGD, respectively. By using a stepwise approach, we have first demonstrated the importance of multivalency for efficient recognition with naturel IgM and α(v)β(3) integrin expressing M21 tumor cell line. Once covalently conjugated by click chemistry, we confirmed by flow cytometry and confocal microscopy that the recognition properties of both the ABM and TBM are conserved, and more importantly, that the resulting ARM promotes the formation of a ternary complex between natural IgM and cancer cells, which is required for the stimulation of the cytotoxic immune response in vivo. Due to the efficiency of the synthetic process, a larger diversity of heterovalent ligands could be easily explored by using the same multivalent approach and could open new perspectives in this field. |
format | Online Article Text |
id | pubmed-6916168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69161682019-12-17 Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells Liet, Benjamin Laigre, Eugénie Goyard, David Todaro, Biagio Tiertant, Claire Boturyn, Didier Berthet, Nathalie Renaudet, Olivier Chemistry Full Papers We have developed a fully synthetic and multifunctional antibody‐recruiting molecule (ARM) to guide natural antibodies already present in the blood stream against cancer cells without pre‐immunization. Our ARM is composed of antibody and tumor binding modules (i.e., ABM and TBM) displaying clustered rhamnose and cyclo‐RGD, respectively. By using a stepwise approach, we have first demonstrated the importance of multivalency for efficient recognition with naturel IgM and α(v)β(3) integrin expressing M21 tumor cell line. Once covalently conjugated by click chemistry, we confirmed by flow cytometry and confocal microscopy that the recognition properties of both the ABM and TBM are conserved, and more importantly, that the resulting ARM promotes the formation of a ternary complex between natural IgM and cancer cells, which is required for the stimulation of the cytotoxic immune response in vivo. Due to the efficiency of the synthetic process, a larger diversity of heterovalent ligands could be easily explored by using the same multivalent approach and could open new perspectives in this field. John Wiley and Sons Inc. 2019-10-15 2019-12-05 /pmc/articles/PMC6916168/ /pubmed/31613028 http://dx.doi.org/10.1002/chem.201903327 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Liet, Benjamin Laigre, Eugénie Goyard, David Todaro, Biagio Tiertant, Claire Boturyn, Didier Berthet, Nathalie Renaudet, Olivier Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells |
title | Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells |
title_full | Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells |
title_fullStr | Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells |
title_full_unstemmed | Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells |
title_short | Multifunctional Glycoconjugates for Recruiting Natural Antibodies against Cancer Cells |
title_sort | multifunctional glycoconjugates for recruiting natural antibodies against cancer cells |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916168/ https://www.ncbi.nlm.nih.gov/pubmed/31613028 http://dx.doi.org/10.1002/chem.201903327 |
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