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Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies
Tumor‐associated macrophages (TAMs) promote the immune suppressive microenvironment inside tumors and are, therefore, considered as a promising target for the next generation of cancer immunotherapies. To repolarize their phenotype into a tumoricidal state, the Toll‐like receptor 7/8 agonist imidazo...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132149/ https://www.ncbi.nlm.nih.gov/pubmed/34026453 http://dx.doi.org/10.1002/advs.202004574 |
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author | Bolli, Evangelia Scherger, Maximilian Arnouk, Sana M. Pombo Antunes, Ana Rita Straßburger, David Urschbach, Moritz Stickdorn, Judith De Vlaminck, Karen Movahedi, Kiavash Räder, Hans Joachim Hernot, Sophie Besenius, Pol Van Ginderachter, Jo A. Nuhn, Lutz |
author_facet | Bolli, Evangelia Scherger, Maximilian Arnouk, Sana M. Pombo Antunes, Ana Rita Straßburger, David Urschbach, Moritz Stickdorn, Judith De Vlaminck, Karen Movahedi, Kiavash Räder, Hans Joachim Hernot, Sophie Besenius, Pol Van Ginderachter, Jo A. Nuhn, Lutz |
author_sort | Bolli, Evangelia |
collection | PubMed |
description | Tumor‐associated macrophages (TAMs) promote the immune suppressive microenvironment inside tumors and are, therefore, considered as a promising target for the next generation of cancer immunotherapies. To repolarize their phenotype into a tumoricidal state, the Toll‐like receptor 7/8 agonist imidazoquinoline IMDQ is site‐specifically and quantitatively coupled to single chain antibody fragments, so‐called nanobodies, targeting the macrophage mannose receptor (MMR) on TAMs. Intravenous injection of these conjugates result in a tumor‐ and cell‐specific delivery of IMDQ into MMR(high) TAMs, causing a significant decline in tumor growth. This is accompanied by a repolarization of TAMs towards a pro‐inflammatory phenotype and an increase in anti‐tumor T cell responses. Therefore, the therapeutic benefit of such nanobody‐drug conjugates may pave the road towards effective macrophage re‐educating cancer immunotherapies. |
format | Online Article Text |
id | pubmed-8132149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81321492021-05-21 Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies Bolli, Evangelia Scherger, Maximilian Arnouk, Sana M. Pombo Antunes, Ana Rita Straßburger, David Urschbach, Moritz Stickdorn, Judith De Vlaminck, Karen Movahedi, Kiavash Räder, Hans Joachim Hernot, Sophie Besenius, Pol Van Ginderachter, Jo A. Nuhn, Lutz Adv Sci (Weinh) Research Articles Tumor‐associated macrophages (TAMs) promote the immune suppressive microenvironment inside tumors and are, therefore, considered as a promising target for the next generation of cancer immunotherapies. To repolarize their phenotype into a tumoricidal state, the Toll‐like receptor 7/8 agonist imidazoquinoline IMDQ is site‐specifically and quantitatively coupled to single chain antibody fragments, so‐called nanobodies, targeting the macrophage mannose receptor (MMR) on TAMs. Intravenous injection of these conjugates result in a tumor‐ and cell‐specific delivery of IMDQ into MMR(high) TAMs, causing a significant decline in tumor growth. This is accompanied by a repolarization of TAMs towards a pro‐inflammatory phenotype and an increase in anti‐tumor T cell responses. Therefore, the therapeutic benefit of such nanobody‐drug conjugates may pave the road towards effective macrophage re‐educating cancer immunotherapies. John Wiley and Sons Inc. 2021-03-08 /pmc/articles/PMC8132149/ /pubmed/34026453 http://dx.doi.org/10.1002/advs.202004574 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Bolli, Evangelia Scherger, Maximilian Arnouk, Sana M. Pombo Antunes, Ana Rita Straßburger, David Urschbach, Moritz Stickdorn, Judith De Vlaminck, Karen Movahedi, Kiavash Räder, Hans Joachim Hernot, Sophie Besenius, Pol Van Ginderachter, Jo A. Nuhn, Lutz Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies |
title | Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies |
title_full | Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies |
title_fullStr | Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies |
title_full_unstemmed | Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies |
title_short | Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies |
title_sort | targeted repolarization of tumor‐associated macrophages via imidazoquinoline‐linked nanobodies |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132149/ https://www.ncbi.nlm.nih.gov/pubmed/34026453 http://dx.doi.org/10.1002/advs.202004574 |
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