Perretti Mauro, Godson Catherine
The William Harvey Research Institute, Barts and The London School of Medicine, Queen Mary University of London, London, UK.
Centre for Inflammation and Therapeutic Innovation, Queen Mary University of London, London, UK.
Br J Pharmacol. 2020 Oct;177(20):4595-4600. doi: 10.1111/bph.15212. Epub 2020 Sep 20.
One way to develop innovative approaches for the treatment of chronic diseases is to exploit the biology of the resolution of inflammation. With this terminology, we identify the integrated and complex network of mediators and pathways that ensure a timely and spatially regulated inflammatory response. Pro-resolving mediators act on specific receptors. This provides an opportunity for developing a new arm of pharmacology we have termed "resolution pharmacology." Here we present the reasoning behind the need to develop new medicines based on resolution and use a prototype GPCR as an example. Understanding how the formyl peptide receptor type 2 (FPR2) operates in a cell-specific manner can guide the development of agonists as new therapeutics that could be of benefit as a therapy or co-therapy for several diseases that affect our society. FPR2 agonists would be among the first drugs to establish "resolution pharmacology" as the pharmacological approach for the third decade of the millennium.
开发慢性疾病创新治疗方法的一种途径是利用炎症消退的生物学机制。用这个术语,我们确定了确保及时和空间调节炎症反应的介质和途径的综合复杂网络。促消退介质作用于特定受体。这为开发我们称为“消退药理学”的新药理学分支提供了机会。在此,我们阐述基于消退开发新药的必要性背后的推理,并以一种原型G蛋白偶联受体为例。了解2型甲酰肽受体(FPR2)如何以细胞特异性方式发挥作用,可以指导激动剂的开发,作为对影响我们社会的几种疾病有益的新疗法或联合疗法。FPR2激动剂将成为将“消退药理学”确立为千禧年第三个十年药理学方法的首批药物之一。