2014
DOI: 10.3109/08923973.2014.968255
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Assessment of 1,25-dihydroxyvitamin D3 effects on Treg cells in a mouse model of systemic lupus erythematosus

Abstract: The remarkable reduction of IL-6 and IL-10 gene expressions, significant enhancement of TGF-β and Foxp3 gene expressions, along with an increase in Treg cell population after oral 1,25-dihydroxyvitamin D3 administration suggest a possible role for this vitamin as a prophylactic supplement in SLE.

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Cited by 29 publications
(16 citation statements)
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“…Our results demonstrated that, in addition to enhancing the number of CD4 + CD25 high Foxp3 + Treg cells, vitamin D treatment increased the expression levels of Foxp3 and TGFβ, while it decreased the expression of IL6. These results are compatible with previously published studies (Jeffery et al, 2009;Kang, Kim, Lee, Kang, & Lee, 2010;Kang et al, 2012;Lavi Arab et al, 2014). Increased levels of TGFβ can positively affect the expression of Foxp3 (Mahon, Gordon, Cruz, Cosman, & Cantorna, 2003).…”
Section: Discussionsupporting
confidence: 93%
“…Our results demonstrated that, in addition to enhancing the number of CD4 + CD25 high Foxp3 + Treg cells, vitamin D treatment increased the expression levels of Foxp3 and TGFβ, while it decreased the expression of IL6. These results are compatible with previously published studies (Jeffery et al, 2009;Kang, Kim, Lee, Kang, & Lee, 2010;Kang et al, 2012;Lavi Arab et al, 2014). Increased levels of TGFβ can positively affect the expression of Foxp3 (Mahon, Gordon, Cruz, Cosman, & Cantorna, 2003).…”
Section: Discussionsupporting
confidence: 93%
“…Vitamin D supplementation (2000, 4000 or 50000 IU weekly for 6 months) in patients with SLE showed positive immunological effects by decreasing IL-17A-producing T cells and increasing FOXP3 expression, confirming the relationship between vitamin D status and immunological balance ( 131 ) . Furthermore, vitamin D consumption attenuated the disease progression and increased the number of regulatory T cells in mouse models ( 132 , 133 ) . In patients with SLE, in vitro treatment with vitamin D (50 n m ) has regulatory effects on apoptosis and cell cycle progression and modifies the expression levels of apoptotic genes ( 134 ) ; in addition, vitamin D intake (400 000 IU followed by 20 000 IU weekly for 12 weeks) can positively modulate endothelial function in patients with stable SLE, reducing cardiovascular risk ( 135 ) .…”
Section: Micronutrientsmentioning
confidence: 99%
“…Neutrophils express VDRs too [78]; studies in SLE showed that, when bound by their ligand 1,25(OH)2D3, the activated VDR mediates an overall improvement of the endothelial damage secondary to the decreased generation of Neutrophils-Extracellular-Traps (NET) [79]. Some of the vitamin D effects observed in vitro were replicated in animal models of lupus, for instance, its ability to favour Treg differentiation and Foxp3 expression [80], to reduce IL-17/23, IFN-gamma and IL-6, and to decrease the titre of anti-dsDNA antibodies [80,81]. A potential therapeutic role for vitamin D in improving clinical manifestations of lupus was hypothesised based on the decreased severity of the disease observed in MRL/1 mice treated with 1,25(OH)2D3 [82].…”
Section: Role Of Vitamin D In the Immune System Regulationmentioning
confidence: 99%