NOD2 and bacterial recognition as therapeutic targets for Crohn's disease

被引:23
作者
de Bruyn, Magali [1 ]
Vermeire, Severine [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Translat Res GastroIntestinal Disorders, Dept Chron Dis Metab & Ageing CHROMETA, Leuven, Belgium
[2] Univ Hosp Leuven, Dept Gastroenterol & Hepatol, Leuven, Belgium
关键词
Crohn's disease; NOD2; risk loci; therapeutic target; INFLAMMATORY-BOWEL-DISEASE; TOLL-LIKE RECEPTOR; NF-KAPPA-B; INTESTINAL EPITHELIAL-CELLS; GENOME-WIDE ASSOCIATION; MURAMYL DIPEPTIDE; GENETIC ASSOCIATION; DENDRITIC CELLS; DIAMINOPIMELIC ACID; SUSCEPTIBILITY LOCI;
D O I
10.1080/14728222.2017.1397627
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Crohn's disease (CD) is a chronic, disabling disease of the gastrointestinal tract that mostly affects young adults. Despite extensive research, the pathogenesis of CD is still not completely understood. It is thought that an abnormal mucosal immune response is elicited towards the luminal microbiota in genetically predisposed persons. Genome-wide association studies and meta-analysis have greatly improved our insight into the genetic background of CD. One of the most studied CD-associated genes is nucleotide-binding oligomerization domain 2 (NOD2).Areas covered: We summarize the current knowledge about NOD2, its use in clinical practice, the functional implications of NOD2 mutations and the therapeutic options for targeting NOD2 in CD.Expert opinion: Almost 2 decades after the identification of NOD2 variants in CD, it has become clear that wild type NOD2 is involved in preserving intestinal barrier integrity and immune homeostasis, properly functioning autophagy and balancing the gut microbiota composition. Given the high prevalence and effect size of NOD2 risk alleles in patients with CD and their interplay with important molecular pathways involved in the disease, NOD2 should seriously be considered as a therapeutic target for CD. Several therapeutic approaches exist and these should be further explored to treat NOD2-related deficiencies in CD.
引用
收藏
页码:1123 / 1139
页数:17
相关论文
共 167 条
[1]   Coordinated regulation of toll-like receptor and NOD2 signaling by k63-linked polyubiquitin chains [J].
Abbott, Derek W. ;
Yang, Yibin ;
Hutti, Jessica E. ;
Madhavarapu, Swetha ;
Kelliher, Michelle A. ;
Cantley, Lewis C. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (17) :6012-6025
[2]   Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease [J].
Abreu, MT ;
Taylor, KD ;
Lin, YC ;
Hang, T ;
Gaiennie, J ;
Landers, CJ ;
Vasiliauskas, EA ;
Kam, LY ;
Rojany, M ;
Papadakis, KA ;
Rotter, JI ;
Targan, SR ;
Yang, HY .
GASTROENTEROLOGY, 2002, 123 (03) :679-688
[3]   Ubiquitin-mediated activation of TAK1 and IKK [J].
Adhikari, A. ;
Xu, M. ;
Chen, Z. J. .
ONCOGENE, 2007, 26 (22) :3214-3226
[4]   The molecular classification of the clinical manifestations of Crohn's disease [J].
Ahmad, T ;
Armuzzi, A ;
Bunce, M ;
Mulcahy-Hawes, K ;
Marshall, SE ;
Orchard, TR ;
Crawshaw, J ;
Large, O ;
De Silva, A ;
Cook, JT ;
Barnardo, M ;
Cullen, S ;
Welsh, KI ;
Jewell, DP .
GASTROENTEROLOGY, 2002, 122 (04) :854-866
[5]   Nod2: The intestinal gate keeper [J].
Al Nabhani, Ziad ;
Dietrich, Gilles ;
Hugot, Jean-Pierre ;
Barreau, Frederick .
PLOS PATHOGENS, 2017, 13 (03)
[6]   Nod2 Deficiency Leads to a Specific and Transmissible Mucosa-associated Microbial Dysbiosis Which Is Independent of the Mucosal Barrier Defect [J].
Al Nabhani, Ziad ;
Lepage, Patricia ;
Mauny, Pascal ;
Montcuquet, Nicolas ;
Roy, Maryline ;
Le Roux, Karine ;
Dussaillant, Monique ;
Berrebi, Dominique ;
Hugot, Jean-Pierre ;
Barreau, Frederick .
JOURNAL OF CROHNS & COLITIS, 2016, 10 (12) :1428-1436
[7]   Respective Roles of Hematopoietic and Nonhematopoietic Nod2 on the Gut Microbiota and Mucosal Homeostasis [J].
Alnabhani, Ziad ;
Hugot, Jean-Pierre ;
Montcuquet, Nicolas ;
Le Roux, Karine ;
Dussaillant, Monique ;
Roy, Maryline ;
Leclerc, Marion ;
Cerf-Bensussan, Nadine ;
Lepage, Patricia ;
Barreau, Frederick .
INFLAMMATORY BOWEL DISEASES, 2016, 22 (04) :763-773
[8]   Nod2 deficiency is associated with an increased mucosal immunoregulatory response to commensal microorganisms [J].
Amendola, A. ;
Butera, A. ;
Sanchez, M. ;
Strober, W. ;
Boirivant, M. .
MUCOSAL IMMUNOLOGY, 2014, 7 (02) :391-404
[9]   Multicenter analysis of fecal microbiota profiles in Japanese patients with Crohn's disease [J].
Andoh, Akira ;
Kuzuoka, Hiroyuki ;
Tsujikawa, Tomoyuki ;
Nakamura, Shiro ;
Hirai, Fumihito ;
Suzuki, Yasuo ;
Matsui, Toshiyuki ;
Fujiyama, Yoshihide ;
Matsumoto, Takayuki .
JOURNAL OF GASTROENTEROLOGY, 2012, 47 (12) :1298-1307
[10]  
[Anonymous], GUT