Maneechotesuwan Kittipong, Supawita Sirinya, Kasetsinsombat Kanda, Wongkajornsilp Adisak, Barnes Peter J
Division of Respiratory Disease and Tuberculosis, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
J Allergy Clin Immunol. 2008 Jan;121(1):43-50. doi: 10.1016/j.jaci.2007.10.011. Epub 2007 Nov 26.
Indoleamine-2, 3-dioxygenase (IDO), a tryptophan-degrading enzyme, plays a key role in the regulation of T-lymphocyte function. IDO inhibits eosinophilic inflammation in a murine asthma model, but little is known about its role in asthmatic patients or the effects of corticosteroids on this key regulatory enzyme.
We studied IDO activity and the effect of inhaled corticosteroids (ICSs) in patients with asthma and how this correlated with eosinophilic inflammation.
After a 1-week run-in period on no therapy, 34 asthmatic patients were treated with only short-acting beta(2)-agonists as required or an ICS or an ICS in combination with a long-acting beta(2)-agonist, which were required for asthma control, and the treatment was continued for a further 4 weeks. Each patient underwent sputum induction at the end of the run-in and treatment periods. Sputum supernatant specimens were analyzed for IDO activity and kynurenine concentrations by using HPLC.
All patients with mild intermittent and mild-to-moderate persistent asthma had low baseline IDO activity in induced sputum compared with that seen in age-matched nonasthmatic subjects. The IDO activity was markedly enhanced by either ICS (P = .03) or ICS/long-acting beta(2)-agonist (P < .0001) treatment, and this increase negatively correlated with sputum eosinophils but was positively associated with an increase in IL-10-positive macrophages.
ICSs might exert their anti-inflammatory activity in asthmatic airways, at least in part, through the upregulation of IDO activity associated with increased IL-10 secretion from macrophages.
吲哚胺-2,3-双加氧酶(IDO)是一种色氨酸降解酶,在T淋巴细胞功能调节中起关键作用。IDO在小鼠哮喘模型中可抑制嗜酸性粒细胞炎症,但对其在哮喘患者中的作用以及皮质类固醇对这种关键调节酶的影响了解甚少。
我们研究了哮喘患者的IDO活性以及吸入性皮质类固醇(ICS)的作用,以及这与嗜酸性粒细胞炎症的相关性。
在1周的无治疗导入期后,34例哮喘患者根据需要仅接受短效β2受体激动剂治疗,或接受ICS治疗,或接受ICS联合长效β2受体激动剂治疗,这些治疗均为哮喘控制所需,且治疗持续4周。每位患者在导入期和治疗期结束时进行痰液诱导。使用高效液相色谱法分析痰液上清液标本中的IDO活性和犬尿氨酸浓度。
与年龄匹配的非哮喘受试者相比,所有轻度间歇性和轻度至中度持续性哮喘患者诱导痰液中的IDO活性基线均较低。ICS(P = 0.03)或ICS/长效β2受体激动剂(P < 0.0001)治疗均可显著提高IDO活性,这种增加与痰液嗜酸性粒细胞呈负相关,但与IL-10阳性巨噬细胞的增加呈正相关。
ICS可能至少部分通过上调与巨噬细胞IL-10分泌增加相关的IDO活性,在哮喘气道中发挥其抗炎活性。