溃疡性结肠炎
1-磷酸鞘氨醇
鞘氨醇-1-磷酸受体
芬戈莫德
鞘氨醇
鞘氨醇激酶
免疫系统
维多利祖马布
药理学
免疫学
医学
生物信息学
神经科学
内科学
生物
疾病
受体
多发性硬化
作者
Silvio Danese,Federica Furfaro,Daniela Gilardi,Giulia Roda,Mariangela Allocca,Laurent Peyrin–Biroulet,Silvio Danese
标识
DOI:10.1080/14712598.2020.1732919
摘要
Introduction: Sphingosine-1-phosphate (S1P) is a membrane-derived lysophospholipid signaling molecule implicated in various physiological and pathological processes, such as regulation of the immune, cardiovascular, pulmonary, and nervous systems and theoretical cancer-related risks, through extracellular activation of S1P1-5 receptors.Areas covered: S1P receptor agonism is a novel strategy for the treatment of UC targeting lymphocyte recirculation, through blockade of lymphocyte egress from lymph nodes. We conducted an extensive literature review on PUBMED on currently available data on molecular aspects of S1P modulation, the mechanisms of action of S1PR agonists (fingolimod, ozanimod, etrasimod, and KRP-203), and their potential efficacy and safety for the treatment of patients with ulcerative colitis.Expert opinion: Selective S1P modulators have emerged to enlarge the efficacy and safety profile of this class of agents. Phase 3 programs should add the potential body of evidence to prove their benefit for the management of UC patients.
科研通智能强力驱动
Strongly Powered by AbleSci AI