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首页> 外文期刊>Journal of Clinical Pharmacy and Therapeutics >Vitamin K1 and Vitamin K2 immunopharmacological effects on the peripheral lymphocytes of healthy subjects and dialysis patients, as estimated by the lymphocyte immunosuppressant sensitivity test
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Vitamin K1 and Vitamin K2 immunopharmacological effects on the peripheral lymphocytes of healthy subjects and dialysis patients, as estimated by the lymphocyte immunosuppressant sensitivity test

机译:维生素K1和维生素K2免疫药物理学作用对健康受试者和透析患者的外周淋巴细胞,如淋巴细胞免疫抑制剂敏感性试验估算

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Summary What is known and objective Renal transplant recipients receive immunosuppressive therapy to prevent acute rejection. We evaluated the immunopharmacological efficacy of vitamin K1 ( VK 1) and vitamin K2 ( VK 2) on T‐cell mitogen‐activated‐peripheral lymphocytes of dialysis patients and healthy subjects. Methods The effects of VK 1 and VK 2 on the T‐cell mitogen‐stimulated proliferation of peripheral blood mononuclear cells ( PBMC s) obtained from 12 healthy subjects and 12 dialysis patients were estimated. Seven cytokines produced from the activated PBMC s were measured by a BD Cytometric Beads Array kit. Regulatory T cells (Tregs) in PBMC s were analysed as CD 4?+? CD 25?+?FoxP3?+? lymphocytes by flow cytometry. Results VK 2 dose‐dependently suppressed the concanavalin A‐stimulated proliferation of PBMC s from healthy subjects and dialysis patients, whereas VK 1 had no significant effect on the PBMC proliferation. VK 1 and VK 2 did not influence the production of most of the Th1/Th2/Th17 cytokines from the activated PBMC s of these subjects, although VK 2 increased the IL ‐4 production from PBMC s of healthy subjects. The Treg percentages in the PBMC s of dialysis patients were markedly decreased compared to healthy PBMC s after the treatment with relatively low concentrations of VK 2. What is new and conclusion The present data suggest that VK 2 has immunosuppressive efficacy. VK 2 may enhance the immunosuppressive efficacies of glucocorticoids while preventing osteoporosis caused by glucocorticoids.
机译:发明内容已知和客观肾移植受者接受免疫抑制治疗以防止急性排斥。我们评估了维生素K1(VK 1)和维生素K2(VK 2)对透析患者及健康受试者的T细胞丝裂原激活 - 周围淋巴细胞的免疫药业疗效。方法估计VK1和VK 2对12个健康受试者和12例透析患者获得的外周血单核细胞(PBMC S)的T细胞丝膜刺激增殖的影响。由活化的PBMC S产生的七种细胞因子通过BD细胞术珠阵列试剂盒测量。分析PBMC S中的调节性T细胞(Tregs)作为CD 4?+? CD 25?+?Foxp3?+?流式细胞术淋巴细胞。结果VK 2剂量依赖性地抑制了来自健康受试者和透析患者PBMC S的康丹林的增殖,而VK1对PBMC增殖没有显着影响。 VK 1和VK 2没有影响来自这些受试者的激活的PBMC S的大多数Th1 / Th2 / Th17细胞因子的产生,尽管VK 2从健康受试者的PBMC S增加了IL-4产生。与相对低浓度的VK 2进行治疗后,透析患者的PBMC S中PBMC S中的Treg百分比显着降低。什么是新的和结论,本数据表明VK 2具有免疫抑制效果。 VK 2可以增强糖皮质激素的免疫抑制效果,同时防止糖皮质激素引起的骨质疏松症。

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