Brisseau G F, Kresta A, Schouten D, Bohnen J M, Shek P N, Fok E, Rotstein O D
Department of Surgery, University of Toronto, Ontario, Canada.
Antimicrob Agents Chemother. 1994 Nov;38(11):2671-5. doi: 10.1128/AAC.38.11.2671.
Liposomal encapsulation of antimicrobial agents has been used to improve drug delivery, particularly against intracellular pathogens. The effect of unilamellar liposomes on macrophage activation in response to Escherichia coli lipopolysaccharide was examined. Liposomes caused a dose- and time-dependent inhibition of tumor necrosis factor release by lipopolysaccharide-treated cells. The accumulation of tumor necrosis factor mRNA transcripts was unaffected, suggesting a posttranscriptional mechanism for this effect. However, induction of macrophage procoagulant activity was unaffected by liposomes, indicating a selective rather than a global inhibition. These data suggest that liposomes used for drug delivery may modulate the host response to infection.
抗菌剂的脂质体包封已被用于改善药物递送,尤其是针对细胞内病原体。研究了单层脂质体对巨噬细胞响应大肠杆菌脂多糖激活的影响。脂质体导致脂多糖处理的细胞释放肿瘤坏死因子呈现剂量和时间依赖性抑制。肿瘤坏死因子mRNA转录本的积累未受影响,表明这种作用存在转录后机制。然而,脂质体未影响巨噬细胞促凝活性的诱导,表明是选择性而非全面性抑制。这些数据表明,用于药物递送的脂质体可能会调节宿主对感染的反应。