Jha Akhilesh, Fisk Marie, Forrester Jamie, Galloway Jacqui, Joseph Jade, Staples Robyn, Sylvester Karl P
Victor Phillip Dahdaleh Heart & Lung Research Institute, Department of Medicine, University of Cambridge, Cambridge, England.
Department of Respiratory Medicine, Cambridge University Hospitals NHS Foundation Trust, Cambridge, England.
Immunother Adv. 2025 Feb 24;5(1):ltaf005. doi: 10.1093/immadv/ltaf005. eCollection 2025.
This study aims to develop a human lung immune challenge model using inhaled Resiquimod (R848), a Toll-like receptor 7/8 agonist, to investigate inflammatory mechanisms involved in the human respiratory mucosa in health and disease. This approach seeks to induce innate immune anti-viral responses in the lungs and blood, with a suitable dose of inhaled R848 that is clinically tolerable. The study will include healthy volunteers and individuals with asthma. The primary outcome is a change in CXCL10, a biomarker representative of anti-viral responses, at 24 hours post-exposure. Secondary outcomes include changes in lung function, physiological parameters, and inflammatory markers, including C-reactive protein and eosinophil counts. This trial involves a single ascending dose, randomized, single-blind, placebo-controlled design. Participants will receive R848 via nebulization in escalating doses from 0.1 to 100 µg/ml or saline placebo. Safety assessments include spirometry, vital signs, and blood samples to monitor systemic and lung-specific immune responses. The study will contribute to understanding immune pathways in asthma and provide a platform for testing novel anti-inflammatory therapeutics. The protocol has been approved by relevant ethics committees and will be disseminated via peer-reviewed publications and open-access data repositories.
本研究旨在开发一种使用吸入式瑞喹莫德(R848,一种Toll样受体7/8激动剂)的人类肺部免疫激发模型,以研究健康和疾病状态下人类呼吸道黏膜中的炎症机制。该方法旨在通过吸入临床上可耐受的合适剂量的R848,在肺部和血液中诱导先天性免疫抗病毒反应。该研究将纳入健康志愿者和哮喘患者。主要结局是暴露后24小时代表抗病毒反应的生物标志物CXCL10的变化。次要结局包括肺功能、生理参数和炎症标志物(包括C反应蛋白和嗜酸性粒细胞计数)的变化。该试验采用单剂量递增、随机、单盲、安慰剂对照设计。参与者将通过雾化吸入递增剂量(从0.1至100µg/ml)的R848或生理盐水安慰剂。安全性评估包括肺功能测定、生命体征和血液样本,以监测全身和肺部特异性免疫反应。该研究将有助于了解哮喘中的免疫途径,并为测试新型抗炎疗法提供一个平台。该方案已获得相关伦理委员会的批准,并将通过同行评审出版物和开放获取数据存储库进行传播。