FOXP3型
促炎细胞因子
白细胞介素2受体
免疫学
慢性阻塞性肺病
CD8型
调节性T细胞
CD3型
细胞因子
恶化
外周血单个核细胞
流式细胞术
医学
T细胞
生物
免疫系统
炎症
内科学
体外
生物化学
作者
Luan Henrique Vasconcelos Alves,Juliana Tiyaki Ito,Francine Maria de Almeida,Luana Michelli de Oliveira,Rafaël Stelmach,lolanda F.L.C. Tibério,Maria Notomi Sato,Fernanda D.T.Q.S. Lopes
标识
DOI:10.1016/j.intimp.2024.112765
摘要
Previous studies have shown that failure to control inflammatory processes mediated by regulatory T (Treg) cells contributes to chronic obstructive pulmonary disease (COPD) development and progression. The activity of Treg cells depends on their phenotypic characteristics: resting Treg (rTreg, CD3+CD4+CD25+FOXP3+CD25++CD45RA+) and activated Treg (aTreg, CD3+CD4+CD25+FOXP3+CD25+++CD45RA-) cells exhibit immunosuppressive activity, while cytokine-secreting T cells (FrIII, CD3+CD4+CD25+FOXP3+CD25++CD45RA-) exhibit proinflammatory activity. Previous findings have shown an increased density of cytokine-secreting T cells in COPD patients experiencing exacerbation. However, the methods for evaluating COPD under stable conditions are lacking.
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