Department of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania, Philadelphia, PA.
Corporal Michael J. Crescenz Veterans Administration Medical Center, Philadelphia, PA.
Int Forum Allergy Rhinol. 2020 Feb;10(2):265-270. doi: 10.1002/alr.22461.
Ketotifen is a second-generation noncompetitive H1-antihistamine and mast-cell stabilizer. It is commonly used to treat or prevent allergic conjunctivitis, asthma, chronic urticaria, anaphylaxis, mast-cell, and other allergic-type disorders. However, it has never been studied in aspirin-exacerbated respiratory disease (AERD), an aggressive phenotype of chronic rhinosinusitis with nasal polyps, where the mast cell plays a prominent role its pathogenesis.
Human sinonasal epithelial cells were grown at an air-liquid interface (ALI). Ketotifen powder was dissolved in saline to make 4 test solutions at 1.04, 2.08, 10.4, and 20.8 µg/mL. Control (saline) or ketotifen solution was added apically to ALI cultures from tissue of 5 unique patients, and ciliary beat frequency (CBF) changes were recorded. Lactate dehydrogenase was measured at 24 and 48 hours to estimate long-term cellular toxicity.
Apical application of ketotifen at all concentrations was neither ciliotoxic nor ciliostimulatory, with no change in CBF over a period of 15 minutes after application. Cellular toxicity for all concentrations at 24 and 48 hours after application was <3% and <7%, respectively, that of lysed cultures.
Topical application of ketotifen to an in vitro model of sinonasal epithelium is safe, as evaluated by CBF and lactate dehydrogenase. Ketotifen is neither ciliotoxic nor ciliostimulatory, and no long-term cellular toxicity was observed. Ketotifen may have promise as a topical nasal rinse in the treatment of AERD.
酮替芬是第二代非竞争性 H1 抗组胺药和肥大细胞稳定剂。它通常用于治疗或预防过敏性结膜炎、哮喘、慢性荨麻疹、过敏反应、肥大细胞和其他过敏型疾病。然而,它从未在阿司匹林加重的呼吸道疾病(AERD)中进行过研究,AERD 是一种伴有鼻息肉的慢性鼻-鼻窦炎的侵袭性表型,其中肥大细胞在其发病机制中起突出作用。
人鼻黏膜上皮细胞在气液界面(ALI)上生长。将酮替芬粉末溶解在盐水中,制成 4 种浓度为 1.04、2.08、10.4 和 20.8μg/ml 的测试溶液。将对照(盐水)或酮替芬溶液加入到来自 5 位患者的组织的 ALI 培养物的顶端,记录纤毛摆动频率(CBF)的变化。在 24 和 48 小时测量乳酸脱氢酶以评估长期细胞毒性。
在所有浓度下,酮替芬的顶端应用既没有纤毛毒性也没有纤毛刺激作用,在应用后 15 分钟内 CBF 没有变化。在应用后 24 和 48 小时,所有浓度的细胞毒性分别为 <3%和 <7%,低于裂解培养物的细胞毒性。
根据 CBF 和乳酸脱氢酶评估,酮替芬在鼻黏膜上皮的体外模型中的应用是安全的。酮替芬既没有纤毛毒性也没有纤毛刺激作用,也没有观察到长期的细胞毒性。酮替芬可能有希望作为治疗 AERD 的局部鼻腔冲洗剂。