Kam L Y, Targan S R
Cedars-Sinai Medical Center and the UCLA School of Medicine, Los Angeles, California 90048, USA.
Curr Opin Gastroenterol. 1999 Jul;15(4):302-7. doi: 10.1097/00001574-199907000-00005.
Cytokine-based therapy for inflammatory bowel disease (IBD) has significantly advanced in the last year. This review highlights some of the exciting progress that has occurred. The efficacy of anti-tumor necrosis factor (TNF) monoclonal antibody therapy in Crohn's disease has promoted further research and the development of other anti-TNF therapies, such as thalidomide, phosphodiesterase type IV inhibitors, and new-generation anti-TNF monoclonal antibodies. Current research is also focused on more proximal events in the inflammatory cascade to modify T-cell regulation and to decrease the production and activity of proinflammatory proteins, cytokines, and nuclear regulatory factors. Concurrently, the emerging role of interleukin (IL)-11, IL-12, and IL-18 in the perpetuation of chronic inflammation continues to stimulate much interest. All of these new advancements reveal an exciting future for IBD therapy.
基于细胞因子的炎症性肠病(IBD)治疗在过去一年取得了显著进展。本综述重点介绍了已取得的一些令人振奋的进展。抗肿瘤坏死因子(TNF)单克隆抗体疗法在克罗恩病中的疗效推动了对其他抗TNF疗法的进一步研究与开发,如沙利度胺、磷酸二酯酶IV型抑制剂以及新一代抗TNF单克隆抗体。当前的研究还聚焦于炎症级联反应中更上游的事件,以调节T细胞并减少促炎蛋白、细胞因子和核调节因子的产生及活性。同时,白细胞介素(IL)-11、IL-12和IL-18在慢性炎症持续存在中的新作用继续引发了广泛关注。所有这些新进展揭示了IBD治疗令人兴奋的未来。