克拉霉素对CRS促炎细胞因子的时间依赖性影响

A. Pratas, Z. Shaida, J. Gavrilovic, C. Philpott
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引用次数: 0

摘要

背景:本研究的目的是评估克拉霉素对慢性鼻窦炎(CRS)炎症反应的时间效应,进一步探讨大环内酯类药物在细胞培养中作为CRS模型的应用及其对免疫系统的作用。方法:检测克拉霉素对几种细胞因子IL-1β、IL-4、IL-5、IL-8和GM-CSF的时间效应。评估孵育前后的样本,以及去除克拉霉素后24小时收集的样本,以确定是否存在任何免疫调节作用。使用ProcartaPlexTM测定法对细胞因子进行定量。结果:在评估的5种细胞因子中,只有IL-1β和IL-8的产生在4h时受到显著抑制。在培养72小时时观察到IL-4水平增加,并在去除后恢复到接近基线水平。IL-8与克拉霉素的相关性最强。在IL-5和GM-CSF的表达之间没有发现差异。结论:本研究表明克拉霉素对CRS炎症反应具有特异性和剂量依赖性的影响。此外,克拉霉素对细胞因子IL-4和IL-8的免疫调节作用因接触克拉霉素的时间长短而异。应考虑进一步研究,以进一步确定暴露时间与细胞因子表达之间的关系,以及CRS病理生理学中的其他“因素”。这可能使我们能够在未来确定CRS患者服用大环内酯类药物的适当持续时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time-dependent effect of clarithromycin on pro-inflammatory cytokines in CRS
Background: The purpose of this study was to assess the time-effect of clarithromycin on the inflammatory response in chronic rhinosinusitis (CRS), to further explore the use of macrolides in cell culture as a model for CRS, and its action on the immune system. Methodology: The time effect of clarithromycin on several cytokines was examined for IL-1β, IL-4, IL-5, IL-8 and GM-CSF. Samples prior and post-incubation were assessed, as well as samples collected 24h following removal of clarithromycin to determine if any immunomodulatory effect persisted. Cytokines were quantified using ProcartaPlexTM assays. Results: Of the 5 cytokines assessed, only IL-1β and IL-8 production were significantly inhibited at 4h. Increased levels of IL-4 were observed at 72 hours of incubation and returned to near baseline levels after its removal. IL-8 showed the most time-dependent relationship with clarithromycin. No differences between the expression of IL-5 and GM-CSF were found. Conclusions: The present work suggests a specific and dose-dependent impact of clarithromycin on the inflammatory response in CRS. Moreover, the immunomodulatory effects of clarithromycin on the cytokines IL-4 and IL-8 varied depending on length of exposure to clarithromycin. Further studies to further establish the relationship between length of exposure and cytokine expression, and with additional “actors” in CRS pathophysiology should be considered. This may enable us in the future to determine appropriate duration of macrolide therapy in patients with CRS.
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