Bravatà Ivana, Fiorino Gionata, Allocca Mariangela, Repici Alessandro, Danese Silvio
Department of Gastroenterology, Endoscopy Unit, Humanitas Research Hospital , Rozzano, Milan , Italy.
Scand J Gastroenterol. 2015 Jan;50(1):113-20. doi: 10.3109/00365521.2014.993700.
Antitumor necrosis factor α agents have dramatically changed the management of inflammatory bowel disease (IBD). However, a significant proportion of patients does not respond or lose response over time. Hence, there is an urgent need for new molecules, with different mechanisms of action, and with a targeted and more effective approach. These new drugs include either small molecules or biological agents. We describe the three most promising classes of molecules in the field of IBD: anti-adhesion, anti-interleukin 12/23 and anti-Janus Kinases therapies.
抗肿瘤坏死因子α制剂极大地改变了炎症性肠病(IBD)的治疗方式。然而,相当一部分患者没有反应或随着时间推移失去反应。因此,迫切需要具有不同作用机制、靶向性更强且更有效的新分子。这些新药包括小分子药物或生物制剂。我们描述了IBD领域中最有前景的三类分子:抗黏附、抗白细胞介素12/23和抗Janus激酶疗法。