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抗 TSLP 抗体对变应原诱导的哮喘反应的影响。

Effects of an anti-TSLP antibody on allergen-induced asthmatic responses.

机构信息

From the Firestone Institute of Respiratory Health, Department of Medicine, McMaster University, Hamilton, ON (G.M.G., P.M.O.), Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University, Quebec City, QC (L.-P.B.), Division of Respirology, Critical Care and Sleep Medicine, University of Saskatchewan, Saskatoon, SK (D.C., B.E.D.), Institute for Heart and Lung Health, University of British Columbia, Vancouver (J.M.F.), and Snyder Institute for Chronic Diseases, Faculty of Medicine, Calgary, AB (R.L.) - all in Canada; Amgen, Thousand Oaks, CA (Y.W., M.B., C.D., K.S.G., L.S., E.B., J.R.P.); and Amgen, Seattle (J.B., M.R.C.).

出版信息

N Engl J Med. 2014 May 29;370(22):2102-10. doi: 10.1056/NEJMoa1402895. Epub 2014 May 20.

Abstract

BACKGROUND

Thymic stromal lymphopoietin (TSLP) is an epithelial-cell-derived cytokine that may be important in initiating allergic inflammation. AMG 157 is a human anti-TSLP monoclonal immunoglobulin G2λ that binds human TSLP and prevents receptor interaction.

METHODS

In this double-blind, placebo-controlled study, we randomly assigned 31 patients with mild allergic asthma to receive three monthly doses of AMG 157 (700 mg) or placebo intravenously. We conducted allergen challenges on days 42 and 84 to evaluate the effect of AMG 157 in reducing the maximum percentage decrease in the forced expiratory volume in 1 second (FEV1). We also measured the fraction of nitric oxide in exhaled air, blood and sputum eosinophils, and airway hyperresponsiveness. The primary end point was the late asthmatic response, as measured 3 to 7 hours after the allergen challenge.

RESULTS

AMG 157 attenuated most measures of allergen-induced early and late asthmatic responses. The maximum percentage decrease in the FEV1 during the late response was 34.0% smaller in the AMG-157 group than in the placebo group on day 42 (P=0.09) and 45.9% smaller on day 84 (P=0.02). In addition, patients receiving AMG 157 had significant decreases in levels of blood and sputum eosinophils before and after the allergen challenge and in the fraction of exhaled nitric oxide. There were 15 adverse events in the AMG-157 group, as compared with 12 in the placebo group; there were no serious adverse events.

CONCLUSIONS

Treatment with AMG 157 reduced allergen-induced bronchoconstriction and indexes of airway inflammation before and after allergen challenge. These findings are consistent with a key role for TSLP in allergen-induced airway responses and persistent airway inflammation in patients with allergic asthma. Whether anti-TSLP therapeutics will have clinical value cannot be determined from these data. (Funded by Amgen; ClinicalTrials.gov number, NCT01405963.).

摘要

背景

胸腺基质淋巴细胞生成素(TSLP)是一种上皮细胞衍生的细胞因子,可能在启动过敏炎症中起重要作用。AMG 157 是一种人源抗 TSLP 单克隆免疫球蛋白 G2λ,可与人类 TSLP 结合并阻止受体相互作用。

方法

在这项双盲、安慰剂对照研究中,我们将 31 例轻度过敏性哮喘患者随机分为三组,分别接受静脉注射 AMG 157(700mg)或安慰剂,每月一次,共三次。在第 42 天和第 84 天进行过敏原挑战,以评估 AMG 157 降低用力呼气量 1 秒(FEV1)最大百分比下降的作用。我们还测量了呼出空气中、血液和痰中嗜酸性粒细胞以及气道高反应性的一氧化氮分数。主要终点是过敏原挑战后 3 至 7 小时测量的晚期哮喘反应。

结果

AMG 157 减弱了大多数过敏原诱导的早期和晚期哮喘反应的指标。在第 42 天,AMG-157 组在晚期反应中 FEV1 的最大百分比下降比安慰剂组小 34.0%(P=0.09),第 84 天下降 45.9%(P=0.02)。此外,接受 AMG 157 治疗的患者在过敏原挑战前后血液和痰中嗜酸性粒细胞水平以及呼出的一氧化氮分数均有显著下降。AMG-157 组有 15 例不良事件,安慰剂组有 12 例;无严重不良事件。

结论

AMG 157 治疗可减少过敏原诱导的支气管收缩和过敏原挑战前后气道炎症的指标。这些发现与 TSLP 在过敏原诱导的气道反应和过敏性哮喘患者持续性气道炎症中的关键作用一致。是否抗 TSLP 治疗具有临床价值尚不能从这些数据中确定。(由 Amgen 资助;ClinicalTrials.gov 编号,NCT01405963)。

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