The Regulation of Intestinal Inflammation and Cancer Development by Type 2 Immune Responses

被引:11
作者
Gamez-Belmonte, Reyes [1 ]
Erkert, Lena [1 ]
Wirtz, Stefan [1 ]
Becker, Christoph [1 ]
机构
[1] Univ Erlangen Nurnberg, Dept Med 1, D-91052 Erlangen, Germany
关键词
intestinal inflammation; colon cancer; type; 2; immunity; IRRITABLE-BOWEL-SYNDROME; MAST-CELLS; COLORECTAL-CANCER; COLON-CANCER; ULCERATIVE-COLITIS; T-CELLS; MACROPHAGE POLARIZATION; RECEPTOR ALPHA-2; TUFT CELLS; EXPRESSION;
D O I
10.3390/ijms21249772
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gut is among the most complex organs of the human body. It has to exert several functions including food and water absorption while setting up an efficient barrier to the outside world. Dysfunction of the gut can be life-threatening. Diseases of the gastrointestinal tract such as inflammatory bowel disease, infections, or colorectal cancer, therefore, pose substantial challenges to clinical care. The intestinal epithelium plays an important role in intestinal disease development. It not only establishes an important barrier against the gut lumen but also constantly signals information about the gut lumen and its composition to immune cells in the bowel wall. Such signaling across the epithelial barrier also occurs in the other direction. Intestinal epithelial cells respond to cytokines and other mediators of immune cells in the lamina propria and shape the microbial community within the gut by producing various antimicrobial peptides. Thus, the epithelium can be considered as an interpreter between the microbiota and the mucosal immune system, safeguarding and moderating communication to the benefit of the host. Type 2 immune responses play important roles in immune-epithelial communication. They contribute to gut tissue homeostasis and protect the host against infections with helminths. However, they are also involved in pathogenic pathways in inflammatory bowel disease and colorectal cancer. The current review provides an overview of current concepts regarding type 2 immune responses in intestinal physiology and pathophysiology.
引用
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页码:1 / 25
页数:24
相关论文
共 178 条
[1]   Fecal Eosinophil Cationic Protein Is a Diagnostic and Predictive Biomarker in Young Adults with Inflammatory Bowel Disease [J].
Abedin, Nada ;
Seemann, Teresa ;
Kleinfeld, Sandra ;
Ruehrup, Jessica ;
Roeseler, Stefani ;
Trautwein, Christian ;
Streetz, Konrad ;
Sellge, Gernot .
JOURNAL OF CLINICAL MEDICINE, 2019, 8 (12)
[2]   Outcomes of inflammatory bowel disease in patients with eosinophil-predominant colonic inflammation [J].
Alhmoud, Tarik ;
Gremida, Anas ;
Steele, Diego Colom ;
Fallahi, Imaneh ;
Tuqan, Wael ;
Nandy, Nina ;
Ismail, Mahmoud ;
Altamimi, Barakat Aburajab ;
Xiong, Meng-Jun ;
Kerwin, Audra ;
Martin, David .
BMJ OPEN GASTROENTEROLOGY, 2020, 7 (01)
[3]   Prognostic significance of faecal eosinophil granule proteins in inflammatory bowel disease [J].
Amcoff, Karin ;
Cao, Yang ;
Zhulina, Yaroslava ;
Lampinen, Maria ;
Halfvarson, Jonas ;
Carlson, Marie .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2019, 54 (10) :1237-1244
[4]   IL-33 Promotes CD11b/CD18-Mediated Adhesion of Eosinophils to Cancer Cells and Synapse-Polarized Degranulation Leading to Tumor Cell Killing [J].
Andreone, Sara ;
Spadaro, Francesca ;
Buccione, Carla ;
Mancini, Jacopo ;
Tinari, Antonella ;
Sestili, Paola ;
Gambardella, Adriana Rosa ;
Lucarini, Valeria ;
Ziccheddu, Giovanna ;
Parolini, Isabella ;
Zanetti, Cristiana ;
D'Urso, Maria Teresa ;
De Ninno, Adele ;
Businaro, Luca ;
Afferni, Claudia ;
Mattei, Fabrizio ;
Schiavoni, Giovanna .
CANCERS, 2019, 11 (11)
[5]  
[Anonymous], 2019, P ACM UBICOMP
[6]  
[Anonymous], 2016, SCI REP UK
[7]  
[Anonymous], 2019, INT J MOL SCI
[8]  
[Anonymous], 2017, SCI REP UK
[9]   Innate lymphoid cells in intestinal cancer development [J].
Atreya, Imke ;
Kindermann, Markus ;
Wirtz, Stefan .
SEMINARS IN IMMUNOLOGY, 2019, 41
[10]   Role of Human Macrophage Polarization in Inflammation during Infectious Diseases [J].
Atri, Chiraz ;
Guerfali, Fatma Z. ;
Laouini, Dhafer .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (06)