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人体首次研究吸入 TLR9 寡核苷酸激动剂 AZD1419 可在肺部引起干扰素反应,且安全耐受良好。

First-in-Human Study With the Inhaled TLR9 Oligonucleotide Agonist AZD1419 Results in Interferon Responses in the Lung, and Is Safe and Well-Tolerated.

机构信息

Dynavax Technologies, Berkeley, California, USA.

Respiratory, Inflammation and Autoimmunity, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.

出版信息

Clin Pharmacol Ther. 2018 Aug;104(2):335-345. doi: 10.1002/cpt.938. Epub 2017 Dec 6.

Abstract

Current asthma treatments address symptoms rather than the underlying disease pathophysiology, a better understanding of which has led to the identification of the Th2 high endotype. The activation of Toll-like receptors to induce Type I interferons directly in the lungs represents a novel therapeutic approach to reset this underlying Th2 pathophysiology with the potential to provide long-term disease modification. We present the nonclinical data and phase I clinical profile of an inhaled TLR9 agonist, AZD1419, a C-type CpG designed to induce interferon in the lung. In healthy volunteers, AZD1419 was found to be safe and well-tolerated. Target engagement in the lung was demonstrated at all dose levels tested. No evidence of tolerization or amplification of responses was evident on repeated dosing and 15.4 mg was defined as the maximum tolerated dose. AZD1419 clinical data supports its continued development as a potentially disease-modifying therapeutic in asthma.

摘要

目前的哮喘治疗方法针对的是症状,而不是潜在的疾病病理生理学,对后者的更好理解导致了 Th2 高表型的确定。Toll 样受体的激活以直接在肺部诱导 I 型干扰素代表了一种重置这种潜在的 Th2 病理生理学的新治疗方法,具有提供长期疾病修饰的潜力。我们介绍了一种吸入性 TLR9 激动剂 AZD1419 的非临床数据和 I 期临床特征,这是一种 C 型 CpG,旨在诱导肺部中的干扰素。在健康志愿者中,AZD1419 被发现是安全且耐受良好的。在所有测试剂量水平均证明了肺部的靶标结合。在重复给药时没有出现耐受或反应放大的证据,15.4mg 被定义为最大耐受剂量。AZD1419 的临床数据支持其作为哮喘潜在的疾病修饰治疗药物的继续开发。

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