Annunziata Pasquale, Cioni Chiara, Mugnaini Claudia, Corelli Federico
Department of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy.
Department of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy.
J Neuroimmunol. 2017 Feb 15;303:66-74. doi: 10.1016/j.jneuroim.2016.12.009. Epub 2016 Dec 23.
COR167, a novel CB2-selective high affinity agonist, was found to significantly inhibit, in a dose-dependent manner, the proliferation of both peripheral blood mononuclear cells and myelin basic protein-reactive T cell lines from normal healthy subjects and patients with relapsing-remitting multiple sclerosis (MS). In MS, a significantly higher inhibition was observed in patients on treatment with disease modifying drugs compared to those naive to treatment. The inhibitory activity of COR167 was exerted through a mixed mechanism involving atypical and incomplete shift of Th1 phenotype towards Th2 phenotype associated with slight reduction of IL-4 and IL-5 as well as strongly reduced levels of Th17-related cytokines. COR167 was also able to reduce in vitro migration of stimulated immunocompetent cells through human brain endothelium associated with a significant reduction of levels of several chemokines. These findings demonstrate that COR167 exerts potent immunomodulatory effects and confirm the cannabinoid CB2 receptor as a novel pharmacological target to counteract neuroinflammation.
COR167是一种新型的CB2选择性高亲和力激动剂,研究发现它能以剂量依赖的方式显著抑制正常健康受试者以及复发缓解型多发性硬化症(MS)患者的外周血单核细胞和髓鞘碱性蛋白反应性T细胞系的增殖。在MS患者中,与未接受治疗的患者相比,接受疾病修饰药物治疗的患者表现出明显更高的抑制作用。COR167的抑制活性是通过一种混合机制发挥的,该机制涉及Th1表型向Th2表型的非典型和不完全转变,同时伴有IL-4和IL-5的轻微减少以及Th17相关细胞因子水平的显著降低。COR167还能够减少刺激后的免疫活性细胞通过人脑内皮细胞的体外迁移,同时几种趋化因子的水平也显著降低。这些发现表明COR167具有强大的免疫调节作用,并证实大麻素CB2受体是对抗神经炎症的新型药理学靶点。