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A combined Phase I and II open-label study on the immunomodulatory effects of seaweed extract nutrient complex

机译:I和II期开放标签研究海藻提取物营养复合物的免疫调节作用

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摘要

Background: Isolated fucoidans from brown marine algae have been shown to have a range of immune-modulating effects. This exploratory study aimed to determine whether a seaweed nutrient complex containing a blend of extracts from three different species of brown algae plus nutrients is safe to administer and has biological potential as an immune modulator. The study was undertaken as an open-label combined Phase I and II study.Methods: Participants (n = 10) were randomized to receive the study medication at either a 100 mg (n = 5) or 1000 mg (n = 5) dose over 4 weeks. The primary outcome measurement was in vivo changes in lymphocyte subsets. The secondary outcome measures were ex vivo changes in T-lymphocyte (CD4 and CD8) activation, phagocytosis of granulocytes and monocytes, T helper 1/T helper 2 cytokines, and serum oxygen radical absorbance capacity.Results: The preparation was found to be safe over the 4 weeks at both doses tested. There were no clinically relevant changes to blood measurements of hemopoietic, hepatic, or renal function. Immunomodulatory measurements showed no dose response between the two doses. The combined results from the two doses demonstrated a significant increase in cytotoxic T cell numbers and phagocytic capacity in monocytes, and a significant decrease in levels of the inflammatory cytokine interleukin 6. A separate analysis of the 100 mg dose (n = 5) alone showed a significant linear component over time (P \u3c 0.05) for phagocytosis by both granulocytes and monocytes.Conclusion: The seaweed nutrient complex was safe to use when taken orally over 4 weeks. The preparation was demonstrated to have potential as an immune modulator, and this bioactivity deserves further exploration.
机译:背景:从褐海藻中分离出的岩藻依聚糖已被证明具有一系列免疫调节作用。这项探索性研究旨在确定含有三种不同褐藻提取物和营养素的海藻营养素复合物是否可以安全施用并且具有作为免疫调节剂的生物学潜力。该研究作为开放标签的I期和II期联合研究进行。方法:将参与者(n = 10)随机接受100 mg(n = 5)或1000 mg(n = 5)剂量的研究药物超过4周。主要的结局指标是淋巴细胞亚群的体内变化。次要结果指标是离体T淋巴细胞(CD4和CD8)活化的变化,粒细胞和单核细胞的吞噬作用,T辅助1 / T辅助2细胞因子和血清氧自由基吸收能力。结果:该制剂被认为是安全的在两个测试剂量下的4周内。造血,肝或肾功能的血液测量没有临床相关变化。免疫调节测量显示两次剂量之间没有剂量反应。两种剂量的综合结果表明单核细胞的细胞毒性T细胞数量和吞噬能力显着增加,炎性细胞因子白介素6的水平显着降低。单独对100 mg剂量(n = 5)的单独分析显示随着时间的推移,粒细胞和单核细胞的吞噬作用呈显着线性关系(P <0.05)。结论:口服海藻营养复合物超过4周即可安全使用。已证明该制剂具有作为免疫调节剂的潜力,并且这种生物活性值得进一步探索。

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