Santini Giuseppe, Mores Nadia, Malerba Mario, Mondino Chiara, Macis Giuseppe, Montuschi Paolo
a Department of Pharmacology, Faculty of Medicine , Catholic University of the Sacred Heart , Rome , Italy.
b Department of Internal Medicine , University of Brescia , Brescia , Italy.
Expert Opin Investig Drugs. 2016 Jun;25(6):639-52. doi: 10.1080/13543784.2016.1175434. Epub 2016 Apr 25.
By activating DP1 and DP2 receptors on immune and non-immune cells, prostaglandin D2 (PGD2), a major metabolic product of cyclo-oxygenase pathway released after IgE-mediated mast cell activation, has pro-inflammatory effects, which are relevant to the pathophysiology of allergic airway disease. At least 15 selective, orally active, DP2 receptor antagonists and one DP1 receptor antagonist (asapiprant) are under development for asthma and/or allergic rhinitis.
In this review, the authors cover the pharmacology of PGD2 and PGD2 receptor antagonists and look at the preclinical, phase I and phase II studies with selective DP1 and DP2 receptor antagonists.
Future research should aim to develop once daily compounds and increase the drug clinical potency which, apart from OC000459 and ADC-3680, seems to be relatively low. Further research and development of DP2 receptor antagonists is warranted, particularly in patients with severe uncontrolled asthma, whose management is a top priority. Pediatric studies, which are not available, are required for assessing the efficacy and safety of this novel drug class in children with asthma and allergic rhinitis. Studies on the efficacy of DP2 receptor antagonists in various asthma phenotypes including: smokers, obese subjects, early vs late asthma onset, fixed vs reversible airflow limitation, are required for establishing their pharmacotherapeutic role.
前列腺素D2(PGD2)是免疫球蛋白E介导的肥大细胞活化后释放的环氧化酶途径的主要代谢产物,通过激活免疫细胞和非免疫细胞上的DP1和DP2受体,具有促炎作用,这与过敏性气道疾病的病理生理学相关。目前至少有15种选择性、口服活性的DP2受体拮抗剂和1种DP1受体拮抗剂(阿沙普兰特)正在研发用于治疗哮喘和/或过敏性鼻炎。
在本综述中,作者阐述了PGD2和PGD2受体拮抗剂的药理学,并探讨了选择性DP1和DP2受体拮抗剂的临床前、I期和II期研究。
未来的研究应致力于开发每日一次给药的化合物,并提高药物的临床效力,目前除了OC000459和ADC - 3680外,药物效力似乎相对较低。DP2受体拮抗剂的进一步研发是必要的,尤其是在重度未控制哮喘患者中,这是治疗的重中之重。需要开展儿科研究(目前尚无相关研究)来评估这类新药在哮喘和过敏性鼻炎儿童中的疗效和安全性。还需要研究DP2受体拮抗剂在各种哮喘表型中的疗效,包括:吸烟者、肥胖者、哮喘早发与晚发、固定性气流受限与可逆性气流受限,以确定其药物治疗作用。