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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...

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Autores principales: Caspar, Birgit, Cocchiara, Pietro, Melet, Armelle, Van Emelen, Kristof, Van der Aa, Annegret, Milligan, Graeme, Herbeuval, Jean-Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Newlands Press Ltd 2022
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.
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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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