Controlled activation of non-specific and specific immune defence mechanisms can beneficially manipulate the host's ability to attack malignant cells. In this context, migration and tissue distribution of immunocompetent cells may be prerequisites for an efficient immune surveillance. The effect of various non-cytotoxic concentrations of the Viscum album L. (mistletoe) preparation Iscadore QuFrF on the locomotory activity of immunomagnetically isolated human CD4+ and CD8+ T lymphocytes from healthy donors was investigated. Cellular migration was examined within a three-dimensional collagen matrix. Donor-dependent variations in baseline activities of spontaneously locomoting T cells were accompanied by individual response patterns of T cells from different donors in the presence of various concentrations of mistletoe preparation (0.25-2.5 micrograms/ml). Using the three-dimensional collagen matrix assay an induction of locomotory activity was detected in a highly reproducible fashion although the optimal concentration of mistletoe preparation and the time point of maximal response were individual for each donor. Our data suggest that the direct stimulation of T-cell migration by mistletoe components may modulate the system of immune surveillance and recognition in patients under mistletoe therapy.

译文

非特异性和特异性免疫防御机制的受控激活可以有利地操纵宿主攻击恶性细胞的能力。在这种情况下,免疫活性细胞的迁移和组织分布可能是有效免疫监视的先决条件。Viscum专辑L的各种非细胞毒性浓度的影响。(槲寄生) 制剂Iscadore QuFrF对来自健康供体的免疫磁分离的人CD4和CD8 T淋巴细胞的运动活性进行了研究。在三维胶原蛋白基质中检查细胞迁移。在存在各种浓度的槲寄生制剂 (0.25-2.5微克/毫升) 的情况下,自发运动的T细胞的基线活性的供体依赖性变化伴随着来自不同供体的T细胞的个体反应模式。使用三维胶原基质测定法,尽管槲寄生制剂的最佳浓度和最大反应的时间点对于每个供体都是单独的,但仍以高度可重复性的方式检测到运动活性的诱导。我们的数据表明,槲寄生成分对T细胞迁移的直接刺激可能会调节槲寄生治疗患者的免疫监视和识别系统。

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