Krishna M T, Chauhan A, Little L, Sampson K, Hawksworth R, Mant T, Djukanovic R, Lee T, Holgate S
University of Southampton, Southampton General Hospital, Mail Point 810, Tremona Road, Southampton SO16 6YD, UK.
J Allergy Clin Immunol. 2001 Jun;107(6):1039-45. doi: 10.1067/mai.2001.115631.
APC 366, a selective inhibitor of mast cell tryptase, has been shown to inhibit antigen-induced early asthmatic response (EAR), late asthmatic response (LAR), and bronchial hyperresponsiveness (BHR) in a sheep model of allergic asthma.
The purpose of this study was to investigate the effects of APC 366 on antigen-induced EAR, LAR, and BHR in mild atopic asthmatics not on any anti-inflammatory therapy.
Sixteen mild atopic asthmatics, each with a demonstrable antigen-induced EAR, LAR, and BHR to histamine, were recruited into this randomized, double-blinded, crossover study. APC 366 (5 mg)/placebo was administered by aerosol inhalation 3 times per day on treatment days 1 through 4. Allergen challenge was carried out on day 4. Histamine challenge was performed the following morning, 1 hour after final dosing.
Subjects were shown to have a significantly smaller overall mean area under the curve for the LAR (P =.012) and mean maximum fall in FEV(1) for the LAR (P =.007) after pretreatment with APC 366 in comparison with placebo. No significant effects on BHR were demonstrable. Although the EAR was reduced by 18% after treatment with APC 366 in comparison with placebo, this was not statistically significant.
Short-term repeated administration of APC 366 significantly reduced the magnitude of antigen-induced LAR in atopic asthmatics, which supports the role of mast cell tryptase in the pathophysiology of the LAR.
APC 366是一种肥大细胞类胰蛋白酶的选择性抑制剂,已证实在过敏性哮喘绵羊模型中,它能抑制抗原诱导的早期哮喘反应(EAR)、迟发性哮喘反应(LAR)以及支气管高反应性(BHR)。
本研究旨在探究APC 366对未接受任何抗炎治疗的轻度特应性哮喘患者抗原诱导的EAR、LAR及BHR的影响。
16名轻度特应性哮喘患者被纳入这项随机、双盲、交叉研究,每名患者对组胺均有可证实的抗原诱导EAR、LAR及BHR。在治疗的第1至4天,每天通过雾化吸入给予APC 366(5毫克)/安慰剂3次。在第4天进行过敏原激发试验。在最后一次给药1小时后的次日早晨进行组胺激发试验。
与安慰剂相比,APC 366预处理后,受试者LAR的曲线下总体平均面积显著更小(P = 0.012),LAR的FEV(1)平均最大下降幅度显著更小(P = 0.007)。对BHR无明显影响。尽管与安慰剂相比,APC 366治疗后EAR降低了18%,但这无统计学意义。
短期重复给予APC 366可显著降低特应性哮喘患者抗原诱导的LAR的程度,这支持了肥大细胞类胰蛋白酶在LAR病理生理学中的作用。