Effects of Azithromycin on Blood Inflammatory Gene Expression and Cytokine Production in Sarcoidosis

IF 4.6 2区 医学 Q1 RESPIRATORY SYSTEM
Lung Pub Date : 2024-09-16 DOI:10.1007/s00408-024-00743-w
Simon D. Fraser, Susannah Thackray-Nocera, Caroline Wright, Rachel Flockton, Sally R. James, Michael G. Crooks, Paul M. Kaye, Simon P. Hart
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引用次数: 0

Abstract

Introduction

In sarcoidosis granulomas, monocyte-derived macrophages are activated by pro-inflammatory cytokines including TNF and IL-6. Current drug treatment for sarcoidosis aims to suppress inflammation but disabling side effects can ensue. The macrolide azithromycin may be anti-inflammatory. We aimed to determine whether treatment with azithromycin affects blood inflammatory gene expression and monocyte functions in sarcoidosis.

Methods

Blood samples were collected from patients with chronic pulmonary sarcoidosis enrolled in a single arm, open label clinical trial who received oral azithromycin 250 mg once daily for 3 months. Whole blood inflammatory gene expression with or without LPS stimulation was measured using a 770-mRNA panel. Phenotypic analysis and cytokine production were conducted by flow cytometry and ELISA after 24h stimulation with growth factors and TLR ligands. mTOR activity was assessed by measuring phosphorylated S6RP.

Results

Differential gene expression analysis indicated a state of heightened myeloid cell activation in sarcoidosis. Compared with controls, sarcoidosis patients showed increased LPS responses for several cytokines and chemokines. Treatment with azithromycin had minimal effect on blood gene expression overall, but supervised clustering analysis identified several chemokine genes that were upregulated. At the protein level, azithromycin treatment increased LPS-stimulated TNF and unstimulated IL-8 production. No other cytokines showed significant changes following azithromycin. Blood neutrophil counts fell during azithromycin treatment whereas mononuclear cells remained stable. Azithromycin had no detectable effects on mTOR activity or activation markers.

Conclusion

Blood myeloid cells are activated in sarcoidosis, but azithromycin therapy did not suppress inflammatory gene expression or cytokine production in blood.

Trial registration: EudraCT 2019-000580-24 (17 May 2019)

Abstract Image

阿奇霉素对肉样瘤病血液炎症基因表达和细胞因子产生的影响
导言在肉芽肿中,单核细胞衍生的巨噬细胞被包括 TNF 和 IL-6 在内的促炎细胞因子激活。目前治疗肉样瘤病的药物旨在抑制炎症,但可能会产生令人丧失能力的副作用。大环内酯类药物阿奇霉素可能具有抗炎作用。我们的目的是确定阿奇霉素治疗是否会影响肉样瘤病的血液炎症基因表达和单核细胞功能。方法收集参加单臂、开放标签临床试验的慢性肺肉样瘤病患者的血液样本,这些患者口服阿奇霉素 250 毫克,每天一次,连续服用 3 个月。使用 770-mRNA 面板测量有无 LPS 刺激的全血炎症基因表达。在生长因子和 TLR 配体刺激 24 小时后,通过流式细胞术和 ELISA 进行表型分析和细胞因子生产。与对照组相比,肉样瘤病患者对多种细胞因子和趋化因子的 LPS 反应增强。使用阿奇霉素治疗对血液基因表达的总体影响很小,但监督聚类分析发现了几个上调的趋化因子基因。在蛋白质水平上,阿奇霉素可增加LPS刺激的TNF和未刺激的IL-8的产生。阿奇霉素治疗后,其他细胞因子没有发生明显变化。在阿奇霉素治疗期间,血液中的中性粒细胞数量下降,而单核细胞数量保持稳定。阿奇霉素对mTOR活性或活化标记物没有可检测到的影响。结论肉样瘤病中的血髓细胞被激活,但阿奇霉素治疗并未抑制血液中炎症基因的表达或细胞因子的产生:EudraCT 2019-000580-24 (2019年5月17日)
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来源期刊
Lung
Lung 医学-呼吸系统
CiteScore
9.10
自引率
10.00%
发文量
95
审稿时长
6-12 weeks
期刊介绍: Lung publishes original articles, reviews and editorials on all aspects of the healthy and diseased lungs, of the airways, and of breathing. Epidemiological, clinical, pathophysiological, biochemical, and pharmacological studies fall within the scope of the journal. Case reports, short communications and technical notes can be accepted if they are of particular interest.
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