Bootsma G P, Koenderman L, Dekhuijzen P N, Festen J, Lammers J W, van Herwaarden C L
Department of Pulmonary Diseases, University Hospital, Nijmegen, The Netherlands.
Allergy. 1998 Jul;53(7):653-61. doi: 10.1111/j.1398-9995.1998.tb03951.x.
Bronchial inflammation plays a central role in asthma. We investigated whether parameters of inflammation were increased in peripheral blood. Furthermore, we tested whether fluticasone propionate (FP), a new inhaled corticosteroid (ICS), and beclomethasone dipropionate (BDP) affected these parameters. FP 750 microg/day and BDP 1500 microg/day were compared in a randomized, crossover study consisting of two 6-week treatment periods, each preceded by a 3-week placebo period. Twenty-one patients with symptomatic asthma completed the study. The results were compared with those of six normal subjects (controls). Immunophenotyping of inflammatory cells was performed in whole blood, and serum eosinophil cationic protein (ECP) was measured. With regard to clinical efficacy, ICS increased PC20 histamine by more than 1.9 doubling doses and FEV1 by more than 0.34 l. The number of CD3/HLA-DR+ lymphocytes was significantly increased in asthmatics compared to the normal subjects, both after placebo (P<0.01) and after therapy (P<0.05). The CD3/HLA-DR+ lymphocytes decreased significantly after treatment with FP (P<0.05). Serum ECP was elevated in patients without ICS and decreased after treatment with BDP (P<0.001). In conclusion, the number of CD3/HLA-DR+ lymphocytes and serum ECP levels were raised in the peripheral blood of symptomatic asthmatics, and decreased by clinically effective doses of ICS. In this respect, FP 750 microg/day was at least as effective as BDP 1500 microg/day.
支气管炎症在哮喘中起核心作用。我们研究了外周血中炎症参数是否升高。此外,我们测试了新型吸入性皮质类固醇(ICS)丙酸氟替卡松(FP)和二丙酸倍氯米松(BDP)是否会影响这些参数。在一项随机交叉研究中,对FP 750微克/天和BDP 1500微克/天进行了比较,该研究包括两个为期6周的治疗期,每个治疗期之前都有一个为期3周的安慰剂期。21例有症状的哮喘患者完成了该研究。将结果与6名正常受试者(对照组)的结果进行比较。对全血中的炎症细胞进行免疫表型分析,并测量血清嗜酸性粒细胞阳离子蛋白(ECP)。关于临床疗效,ICS使组胺PC20增加超过1.9倍剂量,使第一秒用力呼气容积(FEV1)增加超过0.34升。与正常受试者相比,哮喘患者在安慰剂治疗后(P<0.01)和治疗后(P<0.05),CD3/HLA-DR+淋巴细胞数量均显著增加。用FP治疗后,CD3/HLA-DR+淋巴细胞数量显著减少(P<0.05)。未使用ICS的患者血清ECP升高,用BDP治疗后降低(P<0.001)。总之,有症状哮喘患者外周血中CD3/HLA-DR+淋巴细胞数量和血清ECP水平升高,而临床有效剂量的ICS可使其降低。在这方面