» Articles » PMID: 33371444

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

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2020 Dec 29
PMID 33371444
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Colorectal cancer and inulin supplementation: the good, the bad, and the unhelpful.

Oliero M, Alaoui A, McCartney C, Santos M Gastroenterol Rep (Oxf). 2024; 12:goae058.

PMID: 38984069 PMC: 11231048. DOI: 10.1093/gastro/goae058.


Distinct T helper cell-mediated antitumor immunity: T helper 2 cells in focus.

Silva R, Lopes M, Travassos L Cancer Pathog Ther. 2024; 1(1):76-86.

PMID: 38328613 PMC: 10846313. DOI: 10.1016/j.cpt.2022.11.001.


Phytochemicals as Immunomodulatory Molecules in Cancer Therapeutics.

Paudel S, Mishra N, Agarwal R Pharmaceuticals (Basel). 2023; 16(12).

PMID: 38139779 PMC: 10746110. DOI: 10.3390/ph16121652.


Microbial Components and Effector Molecules in T Helper Cell Differentiation and Function.

Lee C, Lee H, Park J, Im S Immune Netw. 2023; 23(1):e7.

PMID: 36911805 PMC: 9995987. DOI: 10.4110/in.2023.23.e7.


Regulation of sleep disorders in patients with traumatic brain injury by intestinal flora based on the background of brain-gut axis.

Zhanfeng N, Liang W, Jing K, Jinbo B, Yanjun C, Hechun X Front Neurosci. 2022; 16:934822.

PMID: 36303945 PMC: 9594989. DOI: 10.3389/fnins.2022.934822.


References
1.
De Zuani M, Dal Secco C, Frossi B . Mast cells at the crossroads of microbiota and IBD. Eur J Immunol. 2018; 48(12):1929-1937. DOI: 10.1002/eji.201847504. View

2.
Saadalla A, Lima M, Tsai F, Osman A, Singh M, Linden D . Cell Intrinsic Deregulated ß-Catenin Signaling Promotes Expansion of Bone Marrow Derived Connective Tissue Type Mast Cells, Systemic Inflammation, and Colon Cancer. Front Immunol. 2019; 10:2777. PMC: 6902090. DOI: 10.3389/fimmu.2019.02777. View

3.
Dames P, Bergann T, Fromm A, Bucker R, Barmeyer C, Krug S . Interleukin-13 affects the epithelial sodium channel in the intestine by coordinated modulation of STAT6 and p38 MAPK activity. J Physiol. 2015; 593(24):5269-82. PMC: 4704517. DOI: 10.1113/JP271156. View

4.
Reichman H, Itan M, Rozenberg P, Yarmolovski T, Brazowski E, Varol C . Activated Eosinophils Exert Antitumorigenic Activities in Colorectal Cancer. Cancer Immunol Res. 2019; 7(3):388-400. DOI: 10.1158/2326-6066.CIR-18-0494. View

5.
Tindemans I, Joosse M, Samsom J . Dissecting the Heterogeneity in T-Cell Mediated Inflammation in IBD. Cells. 2020; 9(1). PMC: 7016883. DOI: 10.3390/cells9010110. View