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CXCR4 as a novel target in immunology: moving away from typical antagonists
CXCR4 has been a target of interest in drug discovery for numerous years. However, so far, most if not all studies focused on finding antagonists of CXCR4 function. Recent studies demonstrate that targeting a minor allosteric pocket of CXCR4 induces an immunomodulating effect in immune cells express...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Newlands Press Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298491/ https://www.ncbi.nlm.nih.gov/pubmed/35875591 http://dx.doi.org/10.4155/fdd-2022-0007 |
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author | Caspar, Birgit Cocchiara, Pietro Melet, Armelle Van Emelen, Kristof Van der Aa, Annegret Milligan, Graeme Herbeuval, Jean-Philippe |
author_facet | Caspar, Birgit Cocchiara, Pietro Melet, Armelle Van Emelen, Kristof Van der Aa, Annegret Milligan, Graeme Herbeuval, Jean-Philippe |
author_sort | Caspar, Birgit |
collection | PubMed |
description | CXCR4 has been a target of interest in drug discovery for numerous years. However, so far, most if not all studies focused on finding antagonists of CXCR4 function. Recent studies demonstrate that targeting a minor allosteric pocket of CXCR4 induces an immunomodulating effect in immune cells expressing CXCR4, connected to the TLR pathway. Compounds binding in this minor pocket seem to be functionally selective with inverse agonistic properties in selected GPCR signaling pathways (G(i) activation), but additional signaling pathways are likely to be involved in the immunomodulating effects. In depth research into these CXCR4-targeted immunomodulators could lead to novel treatment options for (auto)-immune diseases. |
format | Online Article Text |
id | pubmed-9298491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Newlands Press Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92984912022-07-21 CXCR4 as a novel target in immunology: moving away from typical antagonists Caspar, Birgit Cocchiara, Pietro Melet, Armelle Van Emelen, Kristof Van der Aa, Annegret Milligan, Graeme Herbeuval, Jean-Philippe Future Drug Discov Review CXCR4 has been a target of interest in drug discovery for numerous years. However, so far, most if not all studies focused on finding antagonists of CXCR4 function. Recent studies demonstrate that targeting a minor allosteric pocket of CXCR4 induces an immunomodulating effect in immune cells expressing CXCR4, connected to the TLR pathway. Compounds binding in this minor pocket seem to be functionally selective with inverse agonistic properties in selected GPCR signaling pathways (G(i) activation), but additional signaling pathways are likely to be involved in the immunomodulating effects. In depth research into these CXCR4-targeted immunomodulators could lead to novel treatment options for (auto)-immune diseases. Newlands Press Ltd 2022-07-19 2022-06 /pmc/articles/PMC9298491/ /pubmed/35875591 http://dx.doi.org/10.4155/fdd-2022-0007 Text en © 2022 Caspar, Birgit https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Review Caspar, Birgit Cocchiara, Pietro Melet, Armelle Van Emelen, Kristof Van der Aa, Annegret Milligan, Graeme Herbeuval, Jean-Philippe CXCR4 as a novel target in immunology: moving away from typical antagonists |
title | CXCR4 as a novel target in immunology: moving away from typical antagonists |
title_full | CXCR4 as a novel target in immunology: moving away from typical antagonists |
title_fullStr | CXCR4 as a novel target in immunology: moving away from typical antagonists |
title_full_unstemmed | CXCR4 as a novel target in immunology: moving away from typical antagonists |
title_short | CXCR4 as a novel target in immunology: moving away from typical antagonists |
title_sort | cxcr4 as a novel target in immunology: moving away from typical antagonists |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298491/ https://www.ncbi.nlm.nih.gov/pubmed/35875591 http://dx.doi.org/10.4155/fdd-2022-0007 |
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