NHLI, Imperial College, London, UK.
J Allergy Clin Immunol. 2011 Oct;128(4):800-807.e9. doi: 10.1016/j.jaci.2011.05.013. Epub 2011 Jun 29.
IL-13 is a key T(H)2 cytokine that is implicated in allergic responses.
We evaluated the effects of an anti-IL-13-blocking antibody compared with placebo on repeated nasal allergen challenge responses in hay fever patients out of season.
We performed a parallel group double-blind study of anti-IL-13 (single dose, 6 mg/kg intravenously, n = 16) and placebo (n = 15), with an additional open label group given a topical nasal corticosteroid (n = 5). Subjects received intranasal timothy grass pollen (Phleum pratense P5 allergen), and serial samples of nasal mucosal lining fluid were taken by using synthetic absorptive matrix and by nasal lavage.
Administration of anti-IL-13 on day 1 resulted in a significant decrease in IL-13 levels in synthetic absorptive matrix eluates compared with placebo (area under the curve 0-8 hours, change from baseline) during the late phase after nasal allergen challenge on day 5 (P < .05) and day 7 (P < .01). There were no apparent effects of anti-IL-13 treatment on nasal lavage eosinophil numbers or total nasal symptom scores versus placebo. However, in a subgroup with high late-phase IL-13 levels at screening, there was a trend for a decrease in total nasal symptom scores after nasal allergen challenge on day 5, when compared with subjects with low IL-13 levels (P < .10). Nasal fluticasone caused suppression of IL-13 (P < .05 on day 5) as well as IL-5 (P < .01 on day 5) levels in the late phase compared with placebo.
Anti-IL-13 had specific pharmacodynamic action in this nasal allergen challenge model, causing profound inhibition of nasal lining fluid IL-13 responses. In addition, there was a possible effect of anti-IL-13 treatment on total nasal symptom scores in a subgroup with high late-phase nasal IL-13 levels at screening.
IL-13 是一种关键的 T(H)2 细胞因子,与过敏反应有关。
我们评估了抗 IL-13 阻断抗体与安慰剂相比,在花粉症患者非季节期间反复鼻过敏原挑战反应中的效果。
我们进行了一项平行组、双盲研究,比较了抗 IL-13(单剂量,6mg/kg 静脉内,n=16)和安慰剂(n=15),以及另外一组接受局部鼻皮质类固醇治疗的开放标签组(n=5)。受试者接受了皮内 Timothy 草花粉(Phleum pratense P5 过敏原),并通过合成吸收基质和鼻冲洗采集了鼻黏膜衬里液的连续样本。
与安慰剂相比,第 1 天给予抗 IL-13 治疗可导致鼻过敏原挑战后第 5 天和第 7 天(P<0.05 和 P<0.01)晚期合成吸收基质洗脱液中 IL-13 水平的显著降低(0-8 小时 AUC,与基线相比的变化)。与安慰剂相比,抗 IL-13 治疗对鼻冲洗嗜酸性粒细胞计数或总鼻症状评分均无明显影响。然而,在筛选时具有高晚期 IL-13 水平的亚组中,与 IL-13 水平较低的受试者相比,第 5 天鼻过敏原挑战后总鼻症状评分有下降的趋势(P<0.10)。与安慰剂相比,鼻氟替卡松在晚期阶段抑制了 IL-13(第 5 天 P<0.05)和 IL-5(第 5 天 P<0.01)的水平。
抗 IL-13 在这种鼻过敏原挑战模型中具有特定的药效学作用,导致鼻衬里液 IL-13 反应的强烈抑制。此外,在筛选时具有高晚期鼻 IL-13 水平的亚组中,抗 IL-13 治疗可能对总鼻症状评分有影响。