State Key Laboratory of Digital Medical Engineering, Department of Otolaryngology Head and Neck Surgery, Zhongda Hospital, School of Life Sciences and Technology, School of Medicine, Advanced Institute for Life and Health, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, Southeast University, Nanjing, 210096, China.
Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, China.
Adv Sci (Weinh). 2024 Mar;11(11):e2306788. doi: 10.1002/advs.202306788. Epub 2024 Jan 8.
Mutations in OTOFERLIN (OTOF) lead to the autosomal recessive deafness 9 (DFNB9). The efficacy of adeno-associated virus (AAV)-mediated OTOF gene replacement therapy is extensively validated in Otof-deficient mice. However, the clinical safety and efficacy of AAV-OTOF is not reported. Here, AAV-OTOF is generated using good manufacturing practice and validated its efficacy and safety in mouse and non-human primates in order to determine the optimal injection dose, volume, and administration route for clinical trials. Subsequently, AAV-OTOF is delivered into one cochlea of a 5-year-old deaf patient and into the bilateral cochleae of an 8-year-old deaf patient with OTOF mutations. Obvious hearing improvement is detected by the auditory brainstem response (ABR) and the pure-tone audiometry (PTA) in these two patients. Hearing in the injected ear of the 5-year-old patient can be restored to the normal range at 1 month after AAV-OTOF injection, while the 8-year-old patient can hear the conversational sounds. Most importantly, the 5-year-old patient can hear and recognize speech only through the AAV-OTOF-injected ear. This study is the first to demonstrate the safety and efficacy of AAV-OTOF in patients, expands and optimizes current OTOF-related gene therapy and provides valuable information for further application of gene therapies for deafness.
OTOF 基因突变导致常染色体隐性耳聋 9 型(DFNB9)。腺相关病毒(AAV)介导的 OTOF 基因替代疗法在 Otof 缺陷型小鼠中得到了广泛验证。然而,尚未报道 AAV-OTOF 的临床安全性和疗效。本研究采用良好生产规范(GMP)生成 AAV-OTOF,并在小鼠和非人类灵长类动物中验证其疗效和安全性,以确定临床试验的最佳注射剂量、体积和给药途径。随后,将 AAV-OTOF 递送至一位 5 岁耳聋患者的一侧耳蜗和一位携带 OTOF 基因突变的 8 岁耳聋患者的双侧耳蜗。这两名患者的听性脑干反应(ABR)和纯音听阈(PTA)检测均显示出明显的听力改善。在 AAV-OTOF 注射后 1 个月,5 岁患者的注射耳听力可恢复至正常范围,而 8 岁患者可听到会话声音。最重要的是,5 岁患者仅通过 AAV-OTOF 注射耳就能听到并识别言语。本研究首次证明了 AAV-OTOF 在患者中的安全性和疗效,拓展和优化了当前 OTOF 相关基因治疗,并为进一步应用耳聋基因治疗提供了有价值的信息。