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Cellular and cytokine immunoregulation in patients with chronic obstructive pulmonary disease and bronchial asthma

机译:慢性阻塞性肺疾病和支气管哮喘患者的细胞和细胞因子免疫调节

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Background: Different forms of chronic airway inflammation may involve diverse pathogenic elements. In general, deficient defence response is a feature of chronic obstructive pulmonary disease (COPD), whereas distorted immunoregulatory mechanisms lead to development of asthmatic symptoms. In addition to diverse effector mechanisms, the cellular and humoral elements participating in the development of immune response may appear to be different in COPD and bronchial asthma (BA) patients.Aims: To evaluate the immunoregulatory properties of T cells and monocytes in cultures of peripheral blood mononuclear cells (PBMC) and to determine the chosen cytokine profiles in COPD and BA patients.Methods: The microcultures of PBMC from COPD and BA patients were assessed for the T-cell response to mitogens, saturation of interleukin (IL)-2 receptors, T-cell suppressive activity and monokine influence on lymphocyte proliferation. Concomitantly, the cytokine (IL-1β, interleukin-1 receptor antagonist, tumour necrosis factor-α, IL-4, IL-6, IL-8) concentrations were determined in the serum, the broncho-alveolar lavage fluid and in the culture supernatants.Results: The T-lymphocyte reactions (response to phytohaemagglutinin, IL-2 receptor saturation, suppressive activity) were lower in BA pateints than in COPD patients. Reversely, the immunogenic activity of monocytes (IL-1β versus IL-1ra production) was higher in BA patients than in COPD patients. The highest values of cytokine concentrations were found in the culture supernatants. The concentrations of tumour necrosis factor-α , IL-4, IL-6 and IL-8 were significantly higher and the concentration of IL-1ra was lower in BA patients than in COPD patients.Conclusion: The assessments of cellular immunoregulatory properties and cytokine profiles in the cultures of blood mononuclear cells may prove helpful for diagnostic and therapeutic discrimination between BA and COPD patients.
机译:背景:慢性气道炎症的不同形式可能涉及多种致病因素。通常,防御反应不足是慢性阻塞性肺疾病(COPD)的特征,而扭曲的免疫调节机制会导致哮喘症状的发展。除了多种效应机制外,参与COPD和支气管哮喘(BA)的患者中参与免疫应答发展的细胞和体液成分可能也有所不同。目的:评估外周培养物中T细胞和单核细胞的免疫调节特性方法:对COPD和BA患者的PBMC进行微培养,评估其对促细胞分裂剂的T细胞反应,白介素(IL)-2受体的饱和度。 ,T细胞的抑制活性和单因子对淋巴细胞增殖的影响。同时测定血清,支气管肺泡灌洗液和培养物中细胞因子(IL-1β,白介素-1受体拮抗剂,肿瘤坏死因子-α,IL-4,IL-6,IL-8)的浓度。结果:BA患者的T淋巴细胞反应(对植物血凝素的反应,IL-2受体饱和度,抑制活性)低于COPD患者。相反,BA患者中单核细胞的免疫原性活性(IL-1β与IL-1ra产生)高于COPD患者。在培养上清液中发现了最高的细胞因子浓度值。与COPD患者相比,BA患者的肿瘤坏死因子-α,IL-4,IL-6和IL-8的浓度明显升高,IL-1ra的浓度降低。结论:细胞免疫调节特性和细胞因子的评估血液单核细胞培养物中的血流分布图可能有助于区分BA和COPD患者的诊断和治疗。

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