Chemokines and Chemokine Receptors as Therapeutic Targets in Inflammatory Bowel Disease; Pitfalls and Promise

被引:66
|
作者
Trivedi, Palak J. [1 ,2 ,3 ,4 ]
Adams, David H. [1 ,2 ]
机构
[1] Univ Birmingham, Inst Immunol & Immunotherapy, Natl Inst Hlth Res NIHR Birmingham, Birmingham, W Midlands, England
[2] Univ Hosp Birmingham NHS Fdn Trust, Queen Elizabeth Hosp Birmingham, Liver Unit, Birmingham, W Midlands, England
[3] Univ Hosp Birmingham NHS Fdn Trust, Queen Elizabeth Hosp Birmingham, Dept Gastroenterol, Birmingham, W Midlands, England
[4] Univ Birmingham, Inst Translat Med, Ctr Rare Dis, Birmingham, W Midlands, England
来源
关键词
Eldelumab; Mongersen; Vercirnon; PLASMACYTOID DENDRITIC CELLS; INTESTINAL EPITHELIAL-CELLS; ACTIVE CROHNS-DISEASE; SMAD7 ANTISENSE OLIGONUCLEOTIDE; THYMUS-EXPRESSED CHEMOKINE; T-CELLS; ULCERATIVE-COLITIS; INDUCTION THERAPY; SCLEROSING CHOLANGITIS; MUCOSAL IMMUNITY;
D O I
10.1093/ecco-jcc/jjx145
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The principal targets for anti-chemokine therapy in inflammatory bowel disease (IBD) have been the receptors CCR9 and CXCR3 and their respective ligands CCL25 and CXCL10. More recently CCR6 and its ligand CCL20 have also received attention, the expression of the latter in enterocytes being manipulated through Smad7 signalling. These pathways, selected based on their fundamental role in regulating mucosal immunity, have led to the development of several therapeutic candidates that have been tested in early phase clinical trials with variable clinical efficacy. In this article, we appraise the status of chemokine-directed therapy in IBD, review recent developments, and nominate future areas for therapeutic focus.
引用
收藏
页码:S641 / S652
页数:12
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