南印度人群血清GM-CSF、IFN-γ、IL-4和TNF-α浓度升高与烟草烟雾诱导的慢性阻塞性肺疾病的关系

IF 2.6 Q3 IMMUNOLOGY International Journal of Inflammation Pub Date : 2018-08-01 eCollection Date: 2018-01-01 DOI:10.1155/2018/2027856
Ankita Mitra, Sangeetha Vishweswaraiah, Tania Ahalya Thimraj, Mahendra Maheswarappa, Chaya Sindaghatta Krishnarao, Komarla Sundararaja Lokesh, Jayaraj Biligere Siddaiah, Koustav Ganguly, Mahesh Padukudru Anand
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引用次数: 10

摘要

背景:慢性阻塞性肺疾病(COPD)是一种破坏性疾病,药物治疗选择有限,全球以及印度的公共卫生负担非常高。吸烟是印度男性慢性阻塞性肺病的主要原因。涉及控制宿主防御机制的细胞因子调节改变的全身性炎症是COPD发病机制的一个标志。然而,生物标志物发现研究在印度COPD患者中受到限制。方法:我们使用多重免疫分析法评估血清中白细胞介素(IL)-2,4,6,8,10,粒细胞巨噬细胞集落刺激因子(GM-CSF),干扰素γ (IFN-γ)和肿瘤坏死因子α (TNF-α)的浓度[中位数(25 -75百分位数)pg/ml]。我们的研究队列包括来自南印度的30名患有慢性阻塞性肺病的吸烟者(TS COPD)和20名没有慢性阻塞性肺病的吸烟者(TS CONTROL)。研究人群的年龄、性别(男性)和烟草消费(包年)相匹配。慢性阻塞性肺疾病(COPD)的诊断依据全球慢性阻塞性肺疾病倡议(GOLD)的持续性气流阻塞标准,该标准由支气管扩张剂后1秒用力呼气量/用力肺活量(FEV1/FVC)的比值决定。结果:血清GM-CSF [69.64 (46.67, 97.48);36.78 (30.07, 53.88), p = 0.014),干扰素-γ(51.06 (17.00,84.86);11.70 (3.18, 32.81), p = 0.017), il - 4 (9.09 (1.8, 19.9);1.8 (1.8, 4.46);p=0.024], TNF-α [20.68 (5.5, 29.26);3.5 (3.5, 4.5);结论:我们的初步研究显示GM-CSF、IFN-γ、IL-4和TNF-α是南印度人群中可信的COPD易感性生物标志物,需要在更大的队列中进行验证。
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Association of Elevated Serum GM-CSF, IFN-γ, IL-4, and TNF-α Concentration with Tobacco Smoke Induced Chronic Obstructive Pulmonary Disease in a South Indian Population.

Background: Chronic obstructive pulmonary disease (COPD) is a devastating condition with limited pharmacotherapeutic options and exceptionally high public-health burden globally as well as in India. Tobacco smoking is the primary cause for COPD among men in India. Systemic inflammation involving altered regulation of cytokines controlling the host defense mechanism is a hallmark of COPD pathogenesis. However, biomarker discovery studies are limited among Indian COPD patients.

Methods: We assessed the serum concentrations [median (25th-75th percentile) pg/ml] of interleukin (IL)-2,4,6,8,10, granulocyte macrophage colony stimulating factor (GM-CSF), interferon gamma (IFN-γ), and tumor necrosis factor alpha (TNF-α) using a multiplexed immunoassay. Our study cohort consisted of 30 tobacco smokers with COPD (TS COPD) and 20 tobacco smokers without COPD (TS CONTROL) from South India. The study population was matched for age, sex (male), and tobacco consumption (pack-years). COPD was diagnosed according to the global initiative for chronic obstructive lung disease (GOLD) criteria of persistent airflow obstruction determined by the ratio of postbronchodilator forced expiratory volume in 1 second/forced vital capacity (FEV1/FVC) of <0.7. A validated structured questionnaire-based survey [Burden of Obstructive Lung Disease (BOLD) study] and spirometry were performed during house to house visit of the field study. Statistical analysis included nonparametric (two-tailed) Mann-Whitney U and Spearman rank test, as appropriate (significance: p<0.05).

Results: Serum GM-CSF [69.64 (46.67, 97.48); 36.78 (30.07, 53.88), p=0.014], IFN-γ [51.06 (17.00, 84.86); 11.70 (3.18, 32.81), p=0.017], IL-4 [9.09 (1.8, 19.9); 1.8 (1.8, 4.46); p=0.024], and TNF-α [20.68 (5.5, 29.26); 3.5 (3.5, 4.5); p<0.001] concentrations (pg/ml) were increased in TS COPD subjects compared to TS CONTROL. A weak correlation between lung function parameters and cytokine concentrations was detected.

Conclusion: Our pilot study reveals GM-CSF, IFN-γ, IL-4, and TNF-α as plausible COPD susceptibility biomarkers within the investigated South Indian population that needs to be validated in a larger cohort.

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16 weeks
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