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四环素对人类迁移抑制因子产生的抑制作用。

Suppression of the production of migration inhibitory factor in humans by tetracycline.

作者信息

Ganguly R, Pennock D, Kluge R M

出版信息

J Infect Dis. 1983 Sep;148(3):611. doi: 10.1093/infdis/148.3.611.

Abstract

The role of Tc in the suppression of immunity has not been widely evaluated although this antibiotic is often prescribed as a long-term therapy [1]. Sporadic reports have indicated that Tc suppresses cellular immunity [2]. However, no data are available concerning the effects of Tc on lymphokine production, especially in human subjects. Peripheral blood mononuclear cells (2 X 10(6)/ml) were obtained from seven normal volunteers and pulsed with 150 micrograms of con A/ml of medium for 3 hr at 37 C. The procedure was carried out in the presence or absence of Tc in RPMI medium under an atmosphere of 5% CO2. The cells were then pelleted, washed, and resuspended in RPMI medium with or without similar concentrations of Tc. Following incubation for 48 hr, the cells were removed and the supernatant was assayed for MIF activities with the use of guinea pig peritoneal macrophages as indicator cells. A change of greater than or equal to 20% in migration was considered significant [3]. Remarkable inhibition of MIF production was noted in cells obtained from five of seven volunteers in the presence of 3 micrograms and 100 micrograms of Tc/ml. ConA-induced inhibition of migration was almost abolished in cell cultures in the presence of 3 micrograms of Tc/ml. Negative inhibition (accelerated migration) was observed in the presence of 100 micrograms of Tc/ml. Macrophage migration in the presence of 100 micrograms of Tc/ml was greater than the migration of control cells. Thus, it appeared that Tc not only interfered with MIF production but also modulated factors involved in the control of normal cell migration.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尽管这种抗生素常被用作长期治疗药物[1],但其在免疫抑制方面的作用尚未得到广泛评估。零星报道表明,土霉素可抑制细胞免疫[2]。然而,关于土霉素对淋巴因子产生的影响,尤其是对人类受试者的影响,尚无相关数据。从7名正常志愿者身上获取外周血单个核细胞(2×10⁶/ml),并在37℃下用150微克伴刀豆球蛋白A/毫升培养基脉冲处理3小时。该操作在含或不含土霉素的RPMI培养基中,于5%二氧化碳气氛下进行。然后将细胞离心、洗涤,并重新悬浮于含或不含相似浓度土霉素的RPMI培养基中。孵育48小时后,去除细胞,用上豚鼠腹膜巨噬细胞作为指示细胞检测上清液中的巨噬细胞移动抑制因子(MIF)活性。迁移变化大于或等于20%被认为具有显著性[3]。在存在3微克和100微克土霉素/毫升的情况下,7名志愿者中有5人的细胞中观察到MIF产生受到显著抑制。在存在3微克土霉素/毫升的细胞培养物中,伴刀豆球蛋白A诱导的迁移抑制几乎被消除。在存在100微克土霉素/毫升的情况下观察到负抑制(加速迁移)。在存在100微克土霉素/毫升的情况下,巨噬细胞迁移大于对照细胞的迁移。因此,似乎土霉素不仅干扰MIF的产生,还调节参与正常细胞迁移控制的因子。(摘要截短于250字)

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