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- Francesca Sassi
- Department of Medical Science, Gerontology and Bone Metabolic Diseases, University of Turin, 10126 Turin, Italy
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- Cristina Tamone
- Department of Medical Science, Gerontology and Bone Metabolic Diseases, University of Turin, 10126 Turin, Italy
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- Patrizia D’Amelio
- Department of Medical Science, Gerontology and Bone Metabolic Diseases, University of Turin, 10126 Turin, Italy
書誌事項
- 公開日
- 2018-11-03
- 権利情報
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- https://creativecommons.org/licenses/by/4.0/
- DOI
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- 10.3390/nu10111656
- 公開者
- MDPI AG
説明
<jats:p>The classical functions of vitamin D are to regulate calcium-phosphorus homeostasis and control bone metabolism. However, vitamin D deficiency has been reported in several chronic conditions associated with increased inflammation and deregulation of the immune system, such as diabetes, asthma, and rheumatoid arthritis. These observations, together with experimental studies, suggest a critical role for vitamin D in the modulation of immune function. This leads to the hypothesis of a disease-specific alteration of vitamin D metabolism and reinforces the role of vitamin D in maintaining a healthy immune system. Two key observations validate this important non-classical action of vitamin D: first, vitamin D receptor (VDR) is expressed by the majority of immune cells, including B and T lymphocytes, monocytes, macrophages, and dendritic cells; second, there is an active vitamin D metabolism by immune cells that is able to locally convert 25(OH)D3 into 1,25(OH)2D3, its active form. Vitamin D and VDR signaling together have a suppressive role on autoimmunity and an anti-inflammatory effect, promoting dendritic cell and regulatory T-cell differentiation and reducing T helper Th 17 cell response and inflammatory cytokines secretion. This review summarizes experimental data and clinical observations on the potential immunomodulating properties of vitamin D.</jats:p>
収録刊行物
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- Nutrients
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Nutrients 10 (11), 1656-, 2018-11-03
MDPI AG
