Vitamin D3 Treatment Decreases Frequencies of CD16-Positive and TNF-α-Secreting Monocytes in Asthmatic Patients

Background: Previously, we demonstrated that glucocorticoid (GC) treatment of asthmatic patients resulted in decreasing frequencies of monocyte subsets expressing CD16 and capable of releasing TNF-α. Here, we wished to analyze whether the active form of vitamin D, i.e. vitamin D 3 , referred to as 1...

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Veröffentlicht in:International archives of allergy and immunology 2015, Vol.166 (3), p.170-176
Hauptverfasser: Grubczak, Kamil, Lipinska, Danuta, Eljaszewicz, Andrzej, Singh, Paulina, Radzikowska, Urszula, Miklasz, Paula, Dabrowska, Milena, Jablonska, Ewa, Bodzenta-Lukaszyk, Anna, Moniuszko, Marcin
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Sprache:eng
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Zusammenfassung:Background: Previously, we demonstrated that glucocorticoid (GC) treatment of asthmatic patients resulted in decreasing frequencies of monocyte subsets expressing CD16 and capable of releasing TNF-α. Here, we wished to analyze whether the active form of vitamin D, i.e. vitamin D 3 , referred to as 1α,25-dihydroxyvitamin D 3 [1,25-(OH) 2 D 3 ] can exert GC-like proapoptotic effects on CD16-positive monocytes and thus decrease the proinflammatory potential of these cells. Finally, we set out to investigate whether the addition of 1,25-(OH) 2 D 3 would facilitate the use of lower doses of GC without decreasing their anti-inflammatory properties. Methods: Peripheral blood mononuclear cells collected from healthy individuals and asthmatic patients were cultured with 1,25-(OH) 2 D 3 and/or varying doses of GC in the presence or absence of caspase inhibition. The cells were either directly stained for extracellular markers or prestimulated with lipopolysaccharide for the assessment of intracellular cytokine production and then analyzed by flow cytometry. Results: We found that 1,25-(OH) 2 D 3 alone (and in combination with GC) decreased the frequency of CD14++CD16+ and CD14+CD16++ monocytes from asthmatic patients and significantly diminished TNF-α production by the monocytes. With regard to the CD14+CD16++ subset, the monocyte-depleting effects of 1,25-(OH) 2 D 3 were abrogated in the presence of pan-caspase inhibitor, suggesting a proapoptotic mechanism of 1,25-(OH) 2 D 3 action. Interestingly, we found that a combined treatment of 1,25-(OH) 2 D 3 and GC allowed for a 5-fold reduction of the GC dose while maintaining their anti-inflammatory effects. Conclusions: This study has revealed novel immunomodulatory properties of 1,25-(OH) 2 D 3 directed against monocyte subsets capable of TNF-α production. In addition, our data suggest that the introduction of 1,25-(OH) 2 D 3 to anti-inflammatory therapy would possibly allow for the use of lower doses of GC.
ISSN:1018-2438
1423-0097
DOI:10.1159/000380882