POLARIZED ACTIVATION OF HUMAN PERIPHERAL BLOOD PHAGOCYTES BY BACTERIOPHAGE–DERIVED DOUBLESTRANDED RNA (LARIFAN) in vitro

R. Dovhyi
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Abstract

Aim. This study aimed to examine the effect of Larifan on metabolic characteristics of human blood monocytes and granulocytes in vitro. Methods. Four healthy adult men aged 21–26 years were recruited to participate in the study as blood donors. The metabolic profile of human blood monocytes and granulocytes was evaluated by phagocytic activity, reactive oxygen species production, nitric oxide generation, and arginase activity. Phagocytosis of FITC-labeled inactivated Staphylococcus aureus and reactive oxygen species generation were estimated by flow cytometry. Arginase activity was assessed in cell lysates, and nitric oxide generation in supernatants was examined using the Griess reaction. Results. Phagocytic index and reactive oxygen species generation were found to be lower in both human blood monocytes and granulocytes treated with Larifan. The drug caused a dose-dependent increase in nitric oxide production, as well as a decrease in the arginase activity of blood monocytes. Conclusions. Our results indicate the ability of Larifan to reinforce the antiviral properties of resting phagocytes along with containment of oxidative stress development.
细菌衍生的双链核糖核酸(LARIFAN)在体外对人类表皮血液噬菌体的极化激活作用
研究目的本研究旨在探讨 Larifan 对体外人体血液单核细胞和粒细胞代谢特征的影响。研究方法研究招募了四名 21-26 岁的健康成年男性作为献血者。通过吞噬活性、活性氧生成、一氧化氮生成和精氨酸酶活性评估人血单核细胞和粒细胞的代谢特征。通过流式细胞术评估了 FITC 标记的灭活金黄色葡萄球菌的吞噬能力和活性氧的产生。精氨酸酶活性在细胞裂解液中进行评估,一氧化氮的生成在上清液中使用格里斯反应进行检测。结果用 Larifan 处理的人血单核细胞和粒细胞的吞噬指数和活性氧生成都较低。该药物可导致一氧化氮产生量的增加以及血液单核细胞精氨酸酶活性的降低。结论。我们的研究结果表明 Larifan 能够增强静止吞噬细胞的抗病毒特性,同时抑制氧化应激的发展。
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