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IL-33/ST2 axis in autoimmune disease
Leila Shakerian1, Hanieh Kolahdooz2, Mitra Garousi3
1Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Cytokine
|August 30, 2022
Summary
Interleukin-33 (IL-33) has a dual role in autoimmune diseases, acting as both a damaging and protective factor. This review examines the IL-33/ST2 axis in various autoimmune conditions.
Area of Science:
- Immunology
- Autoimmune Diseases
Background:
- Interleukin-33 (IL-33), an IL-1 family member, signals through the ST2 receptor.
- IL-33 influences various immune cells, including mast cells, basophils, eosinophils, NK cells, and T lymphocytes.
- Aberrant IL-33 activity is implicated in numerous inflammatory and immune-mediated conditions like MS, RA, SLE, psoriasis, Sjogren's syndrome, and IBD.
Purpose of the Study:
- To review selected studies on the IL-33/ST2 axis in autoimmune diseases.
- To discuss the dual role of IL-33 as a pathogenic or protective cytokine in these conditions.
Main Methods:
- Literature review of studies investigating the IL-33/ST2 axis.
- Analysis of IL-33's role in specific autoimmune and metabolic diseases.
Main Results:
- The IL-33/ST2 axis can promote pro-inflammatory cytokine release in autoimmune diseases.
- Conversely, IL-33 may exhibit anti-inflammatory properties in certain metabolic diseases, such as type 1 diabetes mellitus.
Conclusions:
- The IL-33/ST2 axis presents a complex and context-dependent role in autoimmune pathogenesis.
- Further research is needed to fully elucidate IL-33's therapeutic potential in immune-mediated disorders.
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