Huang Jia, Bai Xin, Stewart William, Xu Xiaoyang, Zhang Xue-Qing
Shanghai Frontiers Science Center of Drug Target Identification and Delivery, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, Shanghai, China.
National Key Laboratory of Innovative Immunotherapy, Shanghai Jiao Tong University, Shanghai, China.
Nat Commun. 2025 Jul 1;16(1):6013. doi: 10.1038/s41467-025-61114-4.
Asthma exacerbations and steroid resistance occur due to disruption of the airway epithelium, limiting the effectiveness of corticosteroids. Although monoclonal antibodies have progressively emerged as adjunctive therapy for steroid-resistant asthma, there remains a clinical need for targeted anti-inflammatory therapies with better efficacy and fewer off-target effects. Here, we propose the ASCEND (Alternative Steroids Co-delivering with mRNA Encoding Nanobodies) approach, which utilizes inhalable lipid nanoparticles formulated with budesonide (iLNP) to deliver mRNA encoding a thymic stromal lymphopoietin nanobody (mnbTSLP) for the treatment of steroid-resistant asthma. Upon nebulization, mnbTSLP-iLNP targets the lungs, enhancing antiTSLP nanobody production while delivering budesonide. This combined therapy reduces airway inflammation, remodeling, and hyperresponsiveness in murine models. Additionally, mnbTSLP restores the sensitivity of steroid-resistant asthmatic mice to budesonide by inhibiting key inflammatory pathways. The ASCEND approach shows superior effects compared to corticosteroid or antiTSLP antibody treatments, offering a promising strategy for steroid-resistant asthma and potentially other respiratory diseases.
哮喘急性加重和类固醇抵抗是由于气道上皮细胞破坏所致,这限制了皮质类固醇的疗效。尽管单克隆抗体已逐渐成为类固醇抵抗性哮喘的辅助治疗方法,但临床上仍需要疗效更好、脱靶效应更少的靶向抗炎疗法。在此,我们提出了ASCEND(与编码纳米抗体的mRNA共同递送的替代类固醇)方法,该方法利用与布地奈德配制的可吸入脂质纳米颗粒(iLNP)来递送编码胸腺基质淋巴细胞生成素纳米抗体(mnbTSLP)的mRNA,用于治疗类固醇抵抗性哮喘。雾化后,mnbTSLP-iLNP靶向肺部,在递送布地奈德的同时增强抗TSLP纳米抗体的产生。这种联合疗法可减轻小鼠模型中的气道炎症、重塑和高反应性。此外,mnbTSLP通过抑制关键炎症途径恢复类固醇抵抗性哮喘小鼠对布地奈德的敏感性。与皮质类固醇或抗TSLP抗体治疗相比,ASCEND方法显示出更好的效果,为类固醇抵抗性哮喘及潜在的其他呼吸系统疾病提供了一种有前景的策略。