Mercuri Francesca A, Anderson Gary P, Miller Bruce E, Demaison Christophe, Tal-Singer Ruth
ENA Respiratory Pty Ltd, Melbourne, Australia.
Department of Biochemistry and Pharmacology, Faculty of Medicine, Dentistry and Health Sciences, the University of Melbourne, Melbourne, VIC, Australia; Lung Health Research Centre, School of Biomedical Sciences, Faculty of Medicine, Dentistry and Health Sciences, the University of Melbourne, Melbourne, VIC, Australia.
Antiviral Res. 2025 Feb;234:106063. doi: 10.1016/j.antiviral.2024.106063. Epub 2024 Dec 27.
Viral respiratory infection is associated with significant morbidity and mortality. The diversity of viruses implicated, coupled with their propensity for mutation, ignited an interest in host-directed antiviral therapies effective across a wide range of viral variants. Toll-like receptors (TLRs) are potential targets for the development of broad-spectrum antivirals given their central role in host immune defenses. Synthetic agonists of TLRs have been shown to boost protective innate immune responses against respiratory viruses. However, clinical success was hindered by short duration of benefit and/or induction of systemic adverse effects. INNA-051, a TLR2/6 agonist, is in development as an intranasal innate immune enhancer for prophylactic treatment in individuals at risk of complications resulting from respiratory viral infections. In vivo animal studies demonstrated the efficacy as prophylaxis against multiple viruses including SARS-CoV-2, influenza, and rhinovirus. Early clinical trials demonstrated an acceptable safety and tolerability profile. Intranasal delivery to the primary site of infection in humans induced a local innate host defense response characterized by innate immune cell infiltration into the nasal epithelium and activation and antiviral response genes. Taken together, the preclinical and clinical data on INNA-051 support further investigation of its use in community infection settings.
病毒性呼吸道感染与显著的发病率和死亡率相关。涉及的病毒种类多样,再加上它们的突变倾向,引发了人们对能有效对抗多种病毒变体的宿主导向型抗病毒疗法的兴趣。鉴于Toll样受体(TLRs)在宿主免疫防御中的核心作用,它们是开发广谱抗病毒药物的潜在靶点。TLRs的合成激动剂已被证明能增强针对呼吸道病毒的保护性先天免疫反应。然而,临床成功受到获益持续时间短和/或引发全身不良反应的阻碍。INNA-051是一种TLR2/6激动剂,正在开发用作鼻内先天免疫增强剂,用于对有呼吸道病毒感染并发症风险的个体进行预防性治疗。体内动物研究证明了其对包括SARS-CoV-2、流感病毒和鼻病毒在内的多种病毒的预防效果。早期临床试验显示出可接受的安全性和耐受性。在人体内将其递送至感染的主要部位可诱导局部先天宿主防御反应,其特征是先天免疫细胞浸润到鼻上皮中以及激活抗病毒反应基因。综上所述,关于INNA-051的临床前和临床数据支持进一步研究其在社区感染环境中的应用。