CXCR4 as a novel target in immunology: moving away from typical antagonists

Author:

Caspar Birgit123,Cocchiara Pietro4,Melet Armelle123,Van Emelen Kristof5,Van der Aa Annegret5,Milligan Graeme4ORCID,Herbeuval Jean-Philippe123ORCID

Affiliation:

1. CNRS UMR-8601, 45 Rue des Saints-Pères, Paris, F-75006, France

2. Team Chemistry & Biology, Modelling & Immunology for Therapy, CBMIT, Paris, France

3. Université Paris Cité, CNRS, Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques, Paris, F-75006, France

4. Centre for Translational Pharmacology, Institute of Molecular, Cell & Systems Biology, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK

5. Ermium Therapeutics, Pépinière Paris Santé Cochin, 29 Rue du Faubourg Saint-Jacques, Paris, F-75014, France

Abstract

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 (Gi 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.

Funder

European Commission

Agence Nationale de la Recherche

Publisher

Future Science Ltd

Subject

General Medicine

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