Allergy-Immunology Division, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Mediators Inflamm. 2010;2010. doi: 10.1155/2010/727305. Epub 2010 Sep 29.
Interleukin-13 and interferon-γ are important effectors of T-helper cells. Interleukin-13 increases expression of the arachidonic acid-metabolizing enzyme, 15-lipoxygenase-1, in a variety of cell types. 15-lipoxygenase-1 is dramatically elevated in the airways of subjects with asthma. Studies in animals indicate that 15-lipoxygenase-1 contributes to the development of allergic airway inflammation but is protective in some other forms of inflammation. We tested the hypothesis that the ability of interleukin-13 and interferon-γ to counterregulate allergic airway inflammation was potentially mediated by counterregulation of 12/15-lipoxygenase, the mouse ortholog of 15-lipoxygenase-1. The airways of mice were treated with interleukin-13 or interferon-γ one day prior to each of the four allergen exposures. Interleukin-13 augmented and interferon-γ inhibited allergic airway inflammation independently of systemic IgE and mucosal IgA responses but in association with counterregulation of 12/15-lipoxygenase. Interleukin-13 and interferon-γ counterregulate 12/15-lipoxygenase potentially contributing to the effects of these cytokines on allergic airway inflammation.
白细胞介素-13 和干扰素-γ 是 T 辅助细胞的重要效应物。白细胞介素-13 增加了各种细胞类型中花生四烯酸代谢酶 15-脂氧合酶-1 的表达。哮喘患者的气道中 15-脂氧合酶-1 显著升高。动物研究表明,15-脂氧合酶-1 有助于过敏性气道炎症的发展,但在某些其他形式的炎症中具有保护作用。我们检验了这样一个假设,即白细胞介素-13 和干扰素-γ 对抗过敏性气道炎症的能力可能是通过对 12/15-脂氧合酶(15-脂氧合酶-1 的小鼠同源物)的反调节来介导的。在每次过敏原暴露前一天,用白细胞介素-13 或干扰素-γ 处理小鼠气道。白细胞介素-13 增强而干扰素-γ 抑制过敏性气道炎症,与系统性 IgE 和黏膜 IgA 反应无关,但与 12/15-脂氧合酶的反调节有关。白细胞介素-13 和干扰素-γ 反调节 12/15-脂氧合酶,可能有助于这些细胞因子对过敏性气道炎症的影响。