Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
Infectious Diseases & Microbiology Research Group, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Front Immunol. 2018 Mar 13;9:302. doi: 10.3389/fimmu.2018.00302. eCollection 2018.
The mechanisms underlying the non-antimicrobial immunomodulatory properties of macrolides are not well understood.
To systematically review the evidence for the immunomodulatory properties of macrolides in humans and to describe the underlying mechanism and extent of their influence on the innate and adaptive immune system.
A systematic literature search was done in MEDLINE using the OVID interface from 1946 to December 2016 according to the preferred reporting items for systematic reviews and meta-analysis (PRISMA). Original articles investigating the influence of four macrolides (azithromycin, clarithromycin, erythromycin, and roxithromycin) on immunological markers in humans were included.
We identified 22 randomized, controlled trials, 16 prospective cohort studies, and 8 case-control studies investigating 47 different immunological markers (186 measurements) in 1,834 participants. The most frequently reported outcomes were a decrease in the number of neutrophils, and the concentrations of neutrophil elastase, interleukin (IL)-8, IL-6, IL-1beta, tumor necrosis factor (TNF)-alpha, eosinophilic cationic protein, and matrix metalloproteinase 9. Inhibition of neutrophil function was reported more frequently than eosinophil function. A decrease in T helper (Th) 2 cells cytokines (IL-4, IL-5, IL-6) was reported more frequently than a decrease in Th1 cytokines (IL-2, INF-gamma).
Macrolides influence a broad range of immunological mechanisms resulting in immunomodulatory effects. To optimize the treatment of chronic inflammatory diseases by macrolides, further studies are necessary, particularly comparing different macrolides and dose effect relationships.
大环内酯类药物的非抗菌免疫调节特性的机制尚不清楚。
系统评价大环内酯类药物对人类的免疫调节作用,并描述其对固有和适应性免疫系统影响的潜在机制和程度。
使用 OVID 界面,从 1946 年到 2016 年 12 月,在 MEDLINE 上进行了系统文献检索,符合系统评价和荟萃分析的首选报告项目 (PRISMA)。纳入了调查四种大环内酯类药物(阿奇霉素、克拉霉素、红霉素和罗红霉素)对人类免疫标志物影响的原始文章。
我们确定了 22 项随机对照试验、16 项前瞻性队列研究和 8 项病例对照研究,调查了 1834 名参与者的 47 种不同免疫标志物(186 项测量)。报告最多的结果是中性粒细胞数量减少,以及中性粒细胞弹性蛋白酶、白细胞介素 (IL)-8、IL-6、IL-1β、肿瘤坏死因子 (TNF)-α、嗜酸性阳离子蛋白和基质金属蛋白酶 9 的浓度降低。抑制中性粒细胞功能的报道比抑制嗜酸性粒细胞功能的报道更频繁。Th2 细胞细胞因子(IL-4、IL-5、IL-6)的减少比 Th1 细胞因子(IL-2、INF-γ)的减少更为常见。
大环内酯类药物影响广泛的免疫机制,导致免疫调节作用。为了通过大环内酯类药物优化治疗慢性炎症性疾病,需要进一步研究,特别是比较不同的大环内酯类药物和剂量效应关系。