Ishibashi Yasuko, Sung Cathy Yea Won, Grati Mhamed, Chien Wade
Inner Ear Gene Therapy Program, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health, 35A 1F220, 35A Covent Dr., Bethesda, MD 20892, USA; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health, Bethesda, MD, USA.
Laboratory of Hearing Biology and Therapeutics, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health, Bethesda, MD, USA.
Hear Res. 2023 May;432:108735. doi: 10.1016/j.heares.2023.108735. Epub 2023 Mar 11.
Adeno-associated virus (AAV)-mediated inner ear gene therapy is a promising treatment option for hearing loss and dizziness. Several studies have shown that AAV-mediated inner ear gene therapy can be applied to various mouse models of hereditary hearing loss to improve their auditory function. Despite the increase in AAV-based animal and clinical studies aiming to rescue auditory and vestibular functions, little is currently known about the host immune responses to AAV in the mammalian inner ear. It has been reported that the host immune response plays an important role in the safety and efficacy of viral-mediated gene therapy. Therefore, in order for AAV-mediated gene therapy to be successfully and safely translated into patients with hearing loss and dizziness, a better understanding of the host immune responses to AAV in the inner ear is critical. In this review, we summarize the current knowledge on host immune responses to AAV-mediated gene therapy in the mammalian inner ear and other organ systems. We also outline the areas of research that are critical for ensuring the safety and efficacy of AAV-mediated inner ear gene therapy in future clinical and translational studies.
腺相关病毒(AAV)介导的内耳基因治疗是一种治疗听力损失和头晕的有前景的选择。多项研究表明,AAV介导的内耳基因治疗可应用于各种遗传性听力损失的小鼠模型,以改善其听觉功能。尽管旨在挽救听觉和前庭功能的基于AAV的动物和临床研究有所增加,但目前对于哺乳动物内耳中宿主对AAV的免疫反应知之甚少。据报道,宿主免疫反应在病毒介导的基因治疗的安全性和有效性中起着重要作用。因此,为了使AAV介导的基因治疗成功且安全地应用于听力损失和头晕患者,更好地了解内耳中宿主对AAV的免疫反应至关重要。在本综述中,我们总结了目前关于哺乳动物内耳及其他器官系统中宿主对AAV介导的基因治疗的免疫反应的知识。我们还概述了在未来临床和转化研究中确保AAV介导的内耳基因治疗的安全性和有效性的关键研究领域。