Caspar Birgit, Cocchiara Pietro, Melet Armelle, Van Emelen Kristof, Van der Aa Annegret, Milligan Graeme, Herbeuval Jean-Philippe
CNRS UMR-8601, 45 Rue des Saints-Pères, Paris, F-75006, France.
Team Chemistry & Biology, Modelling & Immunology for Therapy, CBMIT, Paris, France.
Future Drug Discov. 2022 Jun;4(2):FDD77. doi: 10.4155/fdd-2022-0007. Epub 2022 Jul 19.
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 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.
多年来,CXCR4一直是药物研发领域的一个热门靶点。然而,到目前为止,即便不是所有研究,也是大多数研究都集中在寻找CXCR4功能的拮抗剂上。最近的研究表明,靶向CXCR4的一个较小的变构口袋会在表达CXCR4的免疫细胞中诱导免疫调节作用,这与Toll样受体(TLR)信号通路相关。结合在这个较小口袋中的化合物似乎在选定的G蛋白偶联受体(GPCR)信号通路(G激活)中具有功能选择性和反向激动特性,但免疫调节作用可能还涉及其他信号通路。对这些靶向CXCR4的免疫调节剂进行深入研究可能会为(自身)免疫性疾病带来新的治疗选择。