INTRODUCTION: Severe asthma is a special clinical problem. CD4(+)CD25(high)CD127(low)Foxp3(+) Tregs play a role in maintaining appropriate immunological response. It is a known fact that Treg cells with CCR5 expression represent strong suppressive activity. It has been shown that a low number or altered function of FoxP3(+) Tregs is associated with the inflammatory process and airway obstruction in asthma. AIM: To evaluate whether CCR5 Tregs expression and surface density on FoxP3(+) Treg cells depend on the severity of asthma. MATERIAL AND METHODS: The study included 50 patients with asthma (25 with severe and 25 with mild-to-moderate asthma). The control group comprised 25 healthy volunteers. The phenotype of CD4(+)CD25(high)CD127(low)Foxp3(+)CCR5(+) cells was evaluated by multicolour flow cytometry. The degree of airflow obstruction was assessed by spirometry as forced expiratory volume in 1 s (FEV(1)) and peak expiratory flow (PEF). RESULTS: The absolute count of FoxP3(+) Treg cells in patients with severe asthma was significantly decreased in comparison with the control group. MFI (median fluorescence intensity) of CCR5 expression on FoxP3(+) Treg cells was significantly decreased in severe asthma compared to the mild-to-moderate asthma and control groups. CCR5 expression on FoxP3(+) Treg cells as MFI positively correlated with lung function parameters FEV(1)% and PEF% in patients with severe asthma. CONCLUSIONS: High CCR5 Tregs expression as MFI is associated with improved in lung function parameters: FEV(1)% and PEF% in patients with severe asthma. The measurement of CCR5 expression on the surface of peripheral blood FoxP3(+) Treg cells as MFI could be an additional tool to estimate the severity of asthma.
Relationship between CCR5(+)FoxP3(+) Treg cells and forced expiratory volume in 1 s, peak expiratory flow in patients with severe asthma.
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作者:Kraszula Åukasz, Eusebio Makandjou-Ola, Kuna Piotr, Pietruczuk MirosÅawa
| 期刊: | Postepy Dermatologii I Alergologii | 影响因子: | 1.700 |
| 时间: | 2021 | 起止号: | 2021 Apr;38(2):262-268 |
| doi: | 10.5114/ada.2021.106202 | ||
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