Gomułka Krzysztof, Liebhart Jerzy, Jaskuła Emilia, Mędrala Wojciech
Department of Internal Medicine, Pneumology and Allergology, Wroclaw Medical University, Wroclaw, Poland.
Laboratory of Clinical Immunology, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw, Poland.
Postepy Dermatol Alergol. 2021 Oct;38(5):850-854. doi: 10.5114/ada.2021.103498. Epub 2021 Nov 5.
Asthma is a complex airway disease with heterogeneity in molecular pathways. Hypersecretion of many cytokines (e.g. vascular endothelial growth factor - VEGF), inflammatory cells infiltration (e.g. eosinophils) and different genetic factors (e.g. gene polymorphism) might be responsible for physiological and pathological changes in the course of this chronic disease.
To reveal the possible expression of activation marker CD69 on eosinophils unstimulated and stimulated by VEGF in patients with asthma. Additionally, the influence of a genetic factor (del18 genotype at -2549 -2567 position in the promoter of the VEGF gene) was considered.
The study involved 122 participants (82 patients with asthma and 40 healthy controls). CD69 expression on peripheral blood eosinophils was detected by flow cytometry without exogenous stimulation and after stimulation with VEGF. Genotyping for VEGF-promoter region was performed using the polymerase chain reaction method.
CD69 was strongly presented ( < 0.05) on unstimulated eosinophils of patients with asthma and del18 genotype in the promoter of the VEGF gene. Stimulation of peripheral eosinophils with VEGF did not induce CD69 expression in a dose-dependent manner.
Our results may suggest the potential contribution of the VEGF gene polymorphism to the spontaneous increase of eosinophils activity (priming) in patients with asthma. In addition, the results show that VEGF is unlikely to significantly activate eosinophils in asthmatics.
哮喘是一种复杂的气道疾病,分子途径存在异质性。许多细胞因子(如血管内皮生长因子 - VEGF)的过度分泌、炎症细胞浸润(如嗜酸性粒细胞)以及不同的遗传因素(如基因多态性)可能是这种慢性疾病过程中生理和病理变化的原因。
揭示哮喘患者中未受刺激和经VEGF刺激的嗜酸性粒细胞上活化标志物CD69的可能表达情况。此外,还考虑了遗传因素(VEGF基因启动子 -2549至 -2567位置的del18基因型)的影响。
该研究纳入了122名参与者(82名哮喘患者和40名健康对照)。通过流式细胞术检测外周血嗜酸性粒细胞在无外源性刺激和经VEGF刺激后的CD69表达。使用聚合酶链反应方法对VEGF启动子区域进行基因分型。
在哮喘患者且VEGF基因启动子具有del18基因型的未受刺激嗜酸性粒细胞上,CD69呈强表达(<0.05)。用VEGF刺激外周嗜酸性粒细胞并未以剂量依赖方式诱导CD69表达。
我们的结果可能提示VEGF基因多态性对哮喘患者嗜酸性粒细胞活性的自发增加(致敏)有潜在贡献。此外,结果表明VEGF不太可能显著激活哮喘患者的嗜酸性粒细胞。