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The Complicated Role of Nuclear Factor Erythroid-Derived 2-Like 2 in Allergy and Asthma
Cheryl E Rockwell1, Yining Jin2, Allison P Boss2
1Department of Pharmacology and Toxicology, College of Human Medicine (C.E.R., Y.J., A.P.B., L.M.K., S.A.), Institute for Integrative Toxicology (C.E.R.), Cell and Molecular Biology Program (C.E.R.), Applied Immunology Center for Education and Research (C.E.R.), Department of Food Science and Human Nutrition (A.P.B.), and College of Osteopathic Medicine (L.M.K.), Michigan State University, East Lansing, Michigan rockwelc@msu.edu.
Abstract:
Nuclear factor erythroid-derived 2-like 2 (Nrf2) is a stress-activated transcription factor that is highly responsive to oxidative stress and electrophilic stimuli. Upon activation, Nrf2 upregulates a battery of cytoprotective genes meant to prevent cell death or damage. In many models of inflammation, Nrf2 protects against the immune response and decreases injury, including in the context of asthma and allergy. However, in some models of asthma and allergy, Nrf2 either does not play a role or can even exacerbate inflammation. In general, the reasons behind these discrepancies are not clear and the mechanisms by which Nrf2 modulates immune response are largely uncharacterized. The aim of this review is to highlight current literature assessing the role of Nrf2 in allergy and asthma to understand Nrf2 as a potential therapeutic target. SIGNIFICANCE STATEMENT: Nuclear factor erythroid-derived 2-like 2 (Nrf2) is an important immune mediator that modulates numerous immune cell types in various inflammatory diseases, including allergy and asthma. There is considerable interest in Nrf2 as a drug target in inflammation, which is complicated by the complex nature of Nrf2 in the immune system. This review focuses on the role of Nrf2 in asthma and allergy, including in regulating immune cell function and in detoxifying xenobiotics that exacerbate these diseases.
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