首页> 外文期刊>Journal of Immunological Methods >Influences of nasal lavage collection-, processing- and storage methods on inflammatory markers — Evaluation of a method for non-invasive sampling of epithelial lining fluid in cystic fibrosis and other respiratory diseases
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Influences of nasal lavage collection-, processing- and storage methods on inflammatory markers — Evaluation of a method for non-invasive sampling of epithelial lining fluid in cystic fibrosis and other respiratory diseases

机译:洗鼻液的收集,处理和储存方法对炎症标志物的影响—评估囊性纤维化和其他呼吸系统疾病中无创上皮内衬液采样方法的评价

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Background: Non-invasive sampling of airway epithelial-lining-fluid by nasal lavage (NL) is an emerging method to monitor allergy, infection and inflammation in patients with respiratory diseases. However, the influences of collection-, processing- and storage-methods have not been sufficiently evaluated and standardized.Methods: Influences of repeated NL, centrifugation setups, repeated freezing and thawing, and protease inhibitors on mediator concentration were evaluated in healthy controls and CF patients, which serve as a model for chronic bacterial infection and inflammation. Polymorphonuclear leukocyte elastase (NE)/myeloperoxidase (MPO)/interleukin (IL)-l/IL-6/ 1L-8 and tumour necrosis factor alpha (TNF) concentrations were measured using ELISA and Multiplex Bead-Arrays.Results: NL-repetition within 0.5-4 h markedly decreased NE, IL-8 and MPO-concentrations for up to 70%. NL centrifugation up to 250 xg for cellular differentiation did not significantly influence mediator concentration in native and processed NL fluid. NL freezing and thawing markedly decreased IL-8 and MPO concentrations by up to 50% while NE remained stable. In contrast to preceding reports, storing at -70degC for >= 5 years led to significantly reduced mediator concentrations in NL compared to contemporary analyses, being most pronounced for IL-1beta, IL-6 and TNFa. Storing of samples in the presence of protease inhibitors led to an increase in marker concentration for IL-8 ( + 27%) and MPO ( + 15%) even after one year of storage.Conclusions: NL is an easy and robust technique for inflammation monitoring of the upper airways. For the first time we have shown that diagnostic NL should be performed only once daily to get comparable results. Whereas NL-fluid can be stored unprocessed at - 70 °C for cytokine analysis over 1-2 years with protease inhibitors supporting stability, >5 years storage as well as repeated freezing and thawing should be avoided.
机译:背景:通过鼻灌洗(NL)对气道上皮-衬里液体进行非侵入性采样是一种新兴方法,用于监测呼吸系统疾病患者的过敏,感染和炎症。但是,尚未充分评估和标准化收集,加工和储存方法的影响。方法:在健康对照和CF中评估重复NL,离心设置,反复冷冻和解冻以及蛋白酶抑制剂对介质浓度的影响。患者,作为慢性细菌感染和炎症的模型。使用ELISA和Multiplex Bead-Arrays测定多形核白细胞弹性蛋白酶(NE)/髓过氧化物酶(MPO)/白介素(IL)-1 / IL-6 / 1L-8和肿瘤坏死因子α(TNF)的浓度。结果:NL重复在0.5-4小时内,NE,IL-8和MPO浓度显着降低达70%。 NL离心至250 xg进行细胞分化并没有显着影响天然和加工NL液中的介质浓度。 NL冻结和解冻可将IL-8和MPO浓度显着降低多达50%,而NE保持稳定。与以前的报告相反,与当代分析相比,在-70℃下存储> = 5年导致NL中介体浓度显着降低,其中IL-1beta,IL-6和TNFa最明显。在存在蛋白酶抑制剂的情况下保存样品会导致IL-8(+ 27%)和MPO(+ 15%)的标记物浓度增加,即使在保存一年后也是如此。监视上呼吸道。第一次,我们表明诊断性NL应该每天仅执行一次,以获得可比的结果。 NL-流体可以在70°C的条件下未经处理保存,用于细胞因子分析的时间为1-2年,而蛋白酶抑制剂可支持稳定性,但应避免保存> 5年以及反复冷冻和解冻。

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