IL-12, IL-23 and IL-17 in IBD: immunobiology and therapeutic targeting

被引:340
|
作者
Moschen, Alexander R. [1 ,2 ]
Tilg, Herbert [2 ]
Raine, Tim [3 ]
机构
[1] Med Univ Innsbruck, Christian Doppler Lab Mucosal Immunol, Innsbruck, Austria
[2] Med Univ Innsbruck, Div Internal Med 1, Dept Med, Innsbruck, Austria
[3] Cambridge Univ Hosp NHS Fdn Trust, Addenbrookes Hosp, Dept Gastroenterol, Cambridge, England
关键词
INFLAMMATORY-BOWEL-DISEASE; INNATE LYMPHOID-CELLS; REFRACTORY CROHNS-DISEASE; REGULATORY T-CELLS; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; ANTIINTERFERON-GAMMA ANTIBODY; GENOME-WIDE ASSOCIATION; ULCERATIVE-COLITIS; DOUBLE-BLIND; AUTOIMMUNE INFLAMMATION;
D O I
10.1038/s41575-018-0084-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
IL-12 and IL-23 are closely related cytokines with important roles in the regulation of tissue inflammation. Converging evidence from studies in mice, human observational studies and population genetics supports the importance of these cytokines in the regulation of mucosal inflammation in the gut in particular. Ustekinumab, a therapeutic antibody targeting both cytokines is now widely licensed for the treatment of Crohn's disease, including in Europe, the USA, Canada and Japan, whilst agents targeting IL-23 specifically are in late-phase clinical trials. We review the emerging understanding of the biology of IL-12 and IL-23, as well as that of their major downstream cytokines, including IL-17. In particular, we discuss how their biology has influenced the development of clinical trials and therapeutic strategies in IBD, as well as how findings from clinical trials, at times surprising, have in turn refocused our understanding of the underlying biology.
引用
收藏
页码:185 / 196
页数:12
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