1,25-dihydroxyvitamin D3 regulates t helper and b lymphocyte responses substantially in drug-naive primary Sjögren’s syndrome patients’ mononuclear cells
Autor: | Deniz Genç, Burcu Günaydin, Merve Sezer Kürkçü, Emine Figen Tarhan |
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Přispěvatelé: | MÜ, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümü, Genç, Deniz, Sezer Kürkçü, Merve, Günaydın, Burcu, Tarhan, Emine Figen |
Rok vydání: | 2021 |
Předmět: |
Adult
Male medicine.medical_specialty medicine.medical_treatment Lymphocyte T-Lymphocytes Primary Sjögren’s syndrome Lymphocyte proliferation CD38 Peripheral blood mononuclear cell CD19 Immunomodulation Calcitriol Memory B Cells Internal medicine 1 25-dihydroxyvitamin D3 medicine Humans IL-2 receptor Memory B cell B-Lymphocytes biology business.industry Interleukin-17 General Medicine Middle Aged Interleukin-10 Endocrinology Cytokine medicine.anatomical_structure Sjogren's Syndrome biology.protein Leukocytes Mononuclear Cytokines Female business |
Zdroj: | Turkish journal of medical sciences. 51(5) |
ISSN: | 1303-6165 |
Popis: | Background/aim: A correlation between vitamin D deficiency and primary Sjogren's syndrome (pSS) has already been described. The limited data has been reported regarding the pathological relevance of vitamin D in primary Sjogren's syndrome. In this study, the peripheral blood mononuclear cells were cocultured with 1,25-dihydroxyvitamin D3 to determine the modulatory effect of vitamin D3 on T and B lymphocyte phenotypes in pSS. Materials and methods: Venous blood samples were collected from 11 patients in the treatment phase and 9 drug-naive pSS patients. Peripheral blood mononuclear cells (PBMC) were isolated and separately cultured in the presence and absence of 1,25-dihydroxyvitamin D3 (10 mM) for 5 days of culture period. Lymphocyte proliferation was analyzed for CFSE signaling via flow cytometry. CD3+CD4+ cells were analyzed for intracellular IFN-gamma and IL-17 expressions. CD19+IgD cells were analyzed for CD38 and CD27 expressions to evaluate naive and total memory B cell subsets. Culture supernatants were analyzed for the IFN-gamma, IL-17, and IL-10 cytokine secretions via flow cytometry. Results: 1,25-dihydroxyvitamin D3 significantly decreased Th lymphocyte proliferative responses in drug-naive (p < 0.005) and treated pSS patients (p < 0.05), and B lymphocyte proliferation in drug-naive pSS PBMC cultures (p < 0.01) compared to mononuclear cell cultures alone. 1,25-dihydroxyvitamin D3 significantly decreased IFN-gamma and IL-17 secreting Th cells in both drug naive (p < 0.005 and p < 0.01, respectively) and treated subjects (p < 0.05 and p < 0.05, respectively) by increasing FoxP3 expressing CD4+CD25+ Treg cell frequency. Plasma B lymphocytes significantly reduced in the presence of 1,25-dihydroxyvitamin D3 in drug naive pSS (p < 0.001) and treated patients (p < 0.05) mononuclear cell cultures compared to PBMC cultures alone. Total memory B cell subsets significantly increased with 1,25-dihydroxyvitamin D3 in drug naive pSS when compared with PBMC cultures alone (p < 0.005). IFN-gamma and IL-17 cytokine levels in culture supernatants significantly reduced (p < 0.05 and p < 0.01, respectively) in drug naive pSS patients' PBMC cultures with 1,25-dihydroxyvitamin D3, and IL-10 levels significantly enhanced in both drug-naive (p < 0.01) and treated pSS patients' PBMC cultures (p < 0.01) in the presence of 1,25-dihydroxyvitamin D3. Conclusion: In conclusion, 1,25-dihydroxyvitamin D3 regulated immune responses in both treated and drug-naive pSS patients, but have a more pronounced modulatory effect on mononuclear cell responses in drug-naive pSS patients. |
Databáze: | OpenAIRE |
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