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慢性阻塞性肺疾病炎症活动的腔室差异

Compartment differences of inflammatory activity in chronic obstructive pulmonary disease.

作者信息

Ji Jie, von Schéele Ida, Bergström Jan, Billing Bo, Dahlén Barbro, Lantz Ann-Sofie, Larsson Kjell, Palmberg Lena

机构信息

Lung and Airway Research, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, 171 77, Sweden.

出版信息

Respir Res. 2014 Aug 26;15(1):104. doi: 10.1186/s12931-014-0104-3.

DOI:10.1186/s12931-014-0104-3
PMID:25155252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4243731/
Abstract

BACKGROUND

Chronic obstructive pulmonary disease (COPD) is associated with local and systemic inflammation. The knowledge of interaction and co-variation of the inflammatory responses in different compartments is meagre.

METHOD

Healthy controls (n = 23), smokers with (n = 28) and without (n = 29) COPD performed spirometry and dental examinations. Saliva, induced sputum, bronchoalveolar lavage (BAL) fluid and serum were collected. Inflammatory markers were assessed in all compartments using ELISA, flow cytometry and RT-PCR.

RESULTS

Negative correlations between lung function and saliva IL-8 and matrix metalloproteinase-9 (MMP-9) were found in smokers with COPD. IL-8 and MMP-9 in saliva correlated positively with periodontal disease as assessed by gingival bleeding in non-smokers.Tumor necrosis factor-α (TNF-α) in saliva, serum and TNF-α mRNA expression on macrophages in BAL-fluid were lower in smokers than in non-smokers. There were positive correlations between soluble TNF-α receptor 1 (sTNFR1) and soluble TNF-α receptor 2 (sTNFR2) in sputum, BAL-fluid and serum in all groups. Sputum interleukin-8 (IL-8) or interleukin-6 (IL-6) was positively correlated with sTNFR1 or sTNFR2 in non-smokers and with sTNFR2 in COPD.

CONCLUSION

Saliva which is convenient to collect and analyse, may be suitable for biomarker assessment of disease activity in COPD. An attenuated TNF-α expression was demonstrated by both protein and mRNA analyses in different compartments suggesting that TNF-α response is altered in moderate and severe COPD. Shedding of TNFR1 or TNFR2 is similarly regulated irrespective of airflow limitation.

摘要

背景

慢性阻塞性肺疾病(COPD)与局部和全身炎症相关。不同腔室中炎症反应的相互作用和共同变化的相关知识匮乏。

方法

健康对照者(n = 23)、患有COPD的吸烟者(n = 28)和未患COPD的吸烟者(n = 29)进行了肺功能测定和牙科检查。收集了唾液、诱导痰、支气管肺泡灌洗(BAL)液和血清。使用酶联免疫吸附测定(ELISA)、流式细胞术和逆转录聚合酶链反应(RT-PCR)评估所有腔室中的炎症标志物。

结果

在患有COPD的吸烟者中,发现肺功能与唾液白细胞介素-8(IL-8)和基质金属蛋白酶-9(MMP-9)之间存在负相关。在非吸烟者中,根据牙龈出血评估,唾液中的IL-8和MMP-9与牙周疾病呈正相关。吸烟者唾液、血清中的肿瘤坏死因子-α(TNF-α)以及BAL液中巨噬细胞上的TNF-α mRNA表达低于非吸烟者。在所有组中,痰液、BAL液和血清中的可溶性TNF-α受体1(sTNFR1)和可溶性TNF-α受体2(sTNFR2)之间存在正相关。在非吸烟者中,痰液白细胞介素-8(IL-8)或白细胞介素-6(IL-6)与sTNFR1或sTNFR2呈正相关,而在COPD患者中与sTNFR2呈正相关。

结论

易于收集和分析的唾液可能适用于COPD疾病活动的生物标志物评估。通过蛋白质和mRNA分析在不同腔室中均证实了TNF-α表达减弱,这表明在中度和重度COPD中TNF-α反应发生了改变。无论气流受限情况如何,TNFR1或TNFR2的脱落受到类似调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/b31ab4aa7677/12931_2014_104_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/b47767b62fbe/12931_2014_104_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/df3aa9f2cb73/12931_2014_104_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/66ac29e49c4d/12931_2014_104_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/b31ab4aa7677/12931_2014_104_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/b47767b62fbe/12931_2014_104_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/df3aa9f2cb73/12931_2014_104_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/66ac29e49c4d/12931_2014_104_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30a/4243731/b31ab4aa7677/12931_2014_104_Fig4_HTML.jpg

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