Department of Family Medicine, Seoul St. Mary's Hospital, The Catholic University, Seoul 137-701, Republic of Korea.
Viral Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Republic of Korea.
Evid Based Complement Alternat Med. 2013;2013:635960. doi: 10.1155/2013/635960. Epub 2013 Dec 12.
A randomized double-blind placebo-controlled immunity study involving 99 healthy volunteers was performed to investigate the effect of poly- γ -glutamate ( γ -PGA) on human natural killer (NK) cell activity in peripheral blood. The volunteers were randomly assigned to one of three groups and orally treated with solutions (25 mL) containing 0 mg (placebo), 250 mg (low dosage), or 500 mg (high dosage) of γ -PGA. Each volunteer took one dose every 12 hours for 8 weeks. Blood samples were drawn before the initial treatment and at the 4th and the 8th weeks of treatment. NK cell activity was assessed by measuring its degranulation, cytokine production, and cytotoxicity against the K562 cell line. Our results revealed that the cytotoxic activities of NK cells from the high-dosage γ -PGA group were significantly higher (P < 0.05 for all comparisons) compared to the low dosage and placebo groups at weeks 4 and 8 after the initial treatment. This increase in the NK cell activity among peripheral blood mononuclear cells (PBMCs) of healthy individuals was also confirmed in vitro (as assessed by the degranulation and cytokine production). These results suggest that the oral administration of γ -PGA induces a cell-mediated immunity by increasing the NK cell activity in humans.
一项涉及 99 名健康志愿者的随机双盲安慰剂对照免疫研究旨在探究聚-γ-谷氨酸(γ-PGA)对人外周血自然杀伤(NK)细胞活性的影响。志愿者被随机分为三组,分别口服含有 0mg(安慰剂)、250mg(低剂量)或 500mg(高剂量)γ-PGA 的溶液(25mL)。每位志愿者每 12 小时服用一次,持续 8 周。在初始治疗前和治疗第 4 周和第 8 周采集血样。通过测量 NK 细胞对 K562 细胞系的脱颗粒、细胞因子产生和细胞毒性来评估 NK 细胞活性。我们的结果表明,与初始治疗后第 4 周和第 8 周的低剂量和安慰剂组相比,高剂量γ-PGA 组 NK 细胞的细胞毒性活性显著更高(所有比较 P < 0.05)。这种健康个体外周血单个核细胞(PBMC)中 NK 细胞活性的增加也在体外得到了证实(通过脱颗粒和细胞因子产生评估)。这些结果表明,γ-PGA 的口服给药通过增加人类 NK 细胞活性诱导细胞介导的免疫。