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Background::The incidence of chronic obstructive pulmonary disease (COPD) complicated with invasive pulmonary aspergillosis (IPA) has increased in the last two decades. The mechanism underpinning susceptibility to and high mortality of COPD complicated with IPA is unclear, and the role of T helper cells 17 (Th17 cells) in the compound disease remains unknown. Therefore, this study aimed to assess the function of Th17 cells in COPD combined with IPA.Methods::COPD, IPA, and COPD+IPA mouse models were established in male wild type C57/BL6 mice. The amounts of Th17 cells and retinoic acid-related orphan receptors γt (RORγt) were tested by flow cytometry. Then, serum interleukin (IL)-17 and IL-23 levels were detected by enzyme-linked immunosorbent assay (ELISA) in the control, COPD, IPA and COPD+IPA groups. In addition, COPD+IPA was induced in IL-17 knockout (KO) mice, for determining the role of Th17 cells in COPD+IPA.Results::Compared with the COPD group, the COPD+IPA group showed higher amounts of blood RORγ

作者:Geng Wan-Ru;He Hang-Yong;Zhang Qing;Tong Zhao-Hui

来源:中华医学杂志英文版 2021 年 134卷 5期

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作者:
Geng Wan-Ru;He Hang-Yong;Zhang Qing;Tong Zhao-Hui
来源:
中华医学杂志英文版 2021 年 134卷 5期
标签:
T helper cells 17 Chronic obstructive pulmonary disease (COPD) Invasive pulmonary aspergillosis (IPA) T helper cells 17 Chronic obstructive pulmonary disease (COPD) Invasive pulmonary aspergillosis (IPA)
Background::The incidence of chronic obstructive pulmonary disease (COPD) complicated with invasive pulmonary aspergillosis (IPA) has increased in the last two decades. The mechanism underpinning susceptibility to and high mortality of COPD complicated with IPA is unclear, and the role of T helper cells 17 (Th17 cells) in the compound disease remains unknown. Therefore, this study aimed to assess the function of Th17 cells in COPD combined with IPA.Methods::COPD, IPA, and COPD+IPA mouse models were established in male wild type C57/BL6 mice. The amounts of Th17 cells and retinoic acid-related orphan receptors γt (RORγt) were tested by flow cytometry. Then, serum interleukin (IL)-17 and IL-23 levels were detected by enzyme-linked immunosorbent assay (ELISA) in the control, COPD, IPA and COPD+IPA groups. In addition, COPD+IPA was induced in IL-17 knockout (KO) mice, for determining the role of Th17 cells in COPD+IPA.Results::Compared with the COPD group, the COPD+IPA group showed higher amounts of blood RORγ

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