AAV-Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness

被引:53
作者
Qi, Jieyu [1 ,2 ,3 ]
Tan, Fangzhi [1 ]
Zhang, Liyan [1 ]
Lu, Ling [4 ]
Zhang, Shanzhong [5 ]
Zhai, Yabo [6 ]
Lu, Yicheng [1 ]
Qian, Xiaoyun [4 ]
Dong, Wenxiu [5 ]
Zhou, Yinyi [1 ]
Zhang, Ziyu [1 ]
Yang, Xuehan [1 ]
Jiang, Lulu [5 ]
Yu, Chaorong [5 ]
Liu, Jiancheng [5 ]
Chen, Tian [1 ]
Wu, Lianqiu [5 ]
Tan, Chang [5 ]
Sun, Sijie [5 ,7 ]
Song, Huaien [7 ]
Shu, Yilai [8 ,9 ,10 ,11 ,12 ]
Xu, Lei [13 ]
Gao, Xia [4 ]
Li, Huawei [8 ,9 ,10 ,11 ,12 ,14 ,15 ]
Chai, Renjie [1 ,2 ,3 ,16 ,17 ]
机构
[1] Southeast Univ, Dept Otolaryngol Head & Neck Surg, State Key Lab Digital Med Engn, Zhongda Hosp,Sch Life Sci & Technol,Adv Inst Life, Nanjing 210096, Peoples R China
[2] Nantong Univ, Coinnovat Ctr Neuroregenerat, Nantong 226001, Peoples R China
[3] Beijing Inst Technol, Aerosp Ctr Hosp, Sch Life Sci, Dept Neurol, Beijing 100081, Peoples R China
[4] Nanjing Univ, Affiliated Drum Tower Hosp, Jiangsu Prov Key Med Discipline Lab, Dept Otolaryngol Head & Neck Surg,Med Sch, Nanjing, Peoples R China
[5] Otovia Therapeut Inc, Suzhou 215101, Peoples R China
[6] Southeast Univ, Sch Med, Nanjing 210009, Peoples R China
[7] Fosun Hlth Capital, Shanghai 200233, Peoples R China
[8] Fudan Univ, ENT Inst, Shanghai 200031, Peoples R China
[9] Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China
[10] Fudan Univ, NHC Key Lab Hearing Med, Shanghai 200032, Peoples R China
[11] Fudan Univ, Eye & ENT Hosp, Dept Otorhinolaryngol, State Key Lab Med Neurobiol, Shanghai 200031, Peoples R China
[12] Fudan Univ, MOE Frontiers Ctr Brain Sci, Shanghai 200031, Peoples R China
[13] Shandong Univ, Shandong Prov ENT Hosp, Dept Otolaryngol Head & Neck Surg, Jinan 250022, Shandong, Peoples R China
[14] Fudan Univ, Inst Brain Sci, Shanghai 200032, Peoples R China
[15] Fudan Univ, Collaborat Innovat Ctr Brain Sci, Shanghai 200032, Peoples R China
[16] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Dept Otolaryngol Head & Neck Surg, Chengdu 610072, Peoples R China
[17] Southeast Univ, Shenzhen Res Inst, Shenzhen 518063, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
AAV; biosafety; clinical trial; hearing recovery; OTOF gene therapy; MOUSE MODEL; RESCUES HEARING; OTOF MUTATIONS; ENABLES SAFE; OTOFERLIN; OUTCOMES; BALANCE;
D O I
10.1002/advs.202306788
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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. This study evaluates the efficacy and safety of an adeno-associated virus (AAV) based gene therapy AAV-OTOF in patients with DFNB9 deafness. AAV-OTOF injection can restore the hearing function of the previous deaf ear to a normal level with safety. This proof of concept study provides clinical gene therapy data for DFNB9 deafness and also supplies support for other inner ear gene therapies.image
引用
收藏
页数:13
相关论文
共 50 条
[31]   AAV-mediated gene expression and deletion in cardiac fibroblasts in vivo [J].
Nieto, Bridget ;
Cypress, Michael ;
O-Uchi, Jin ;
Jhun, Bong Sook .
PHYSIOLOGY, 2023, 38
[32]   AAV-mediated gene therapies for glaucoma and uveitis: are we there yet? [J].
Castro, Brenda ;
Steel, Jason C. ;
Layton, Christopher J. .
EXPERT REVIEWS IN MOLECULAR MEDICINE, 2024, 26
[33]   Recombinant AAV-mediated gene delivery to the central nervous system [J].
Tenenbaum, L ;
Chtarto, A ;
Lehtonen, E ;
Velu, T ;
Brotchi, J ;
Levivier, M .
JOURNAL OF GENE MEDICINE, 2004, 6 :S212-S222
[34]   Immunity and AAV-mediated gene therapy for muscular dystrophies in large animal models and human trials [J].
Wang, Zejing ;
Tapscott, Stephen J. ;
Chamberlain, Jeffrey S. ;
Storb, Rainer .
FRONTIERS IN MICROBIOLOGY, 2011, 2
[35]   Current Challenges and Future Directions in Recombinant AAV-Mediated Gene Therapy of Duchenne Muscular Dystrophy [J].
Okada, Takashi ;
Takeda, Shin'ichi .
PHARMACEUTICALS, 2013, 6 (07) :813-836
[36]   AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs [J].
Pichard, Virginie ;
Provost, Nathalie ;
Mendes-Madeira, Alexandra ;
Libeau, Lyse ;
Hulin, Philippe ;
Tshilenge, Kizito-Tshitoko ;
Biget, Marine ;
Ameline, Baptiste ;
Deschamps, Jack-Yves ;
Weber, Michel ;
Le Meur, Guylene ;
Colle, Marie-Anne ;
Moullier, Philippe ;
Rolling, Fabienne .
MOLECULAR THERAPY, 2016, 24 (05) :867-876
[37]   Treatment of skeletal and non-skeletal alterations of Mucopolysaccharidosis type IVA by AAV-mediated gene therapy [J].
Bertolin, Joan ;
Sanchez, Victor ;
Ribera, Albert ;
Jaen, Maria Luisa ;
Garcia, Miquel ;
Pujol, Anna ;
Sanchez, Xavier ;
Munoz, Sergio ;
Marco, Sara ;
Perez, Jennifer ;
Elias, Gemma ;
Leon, Xavier ;
Roca, Carles ;
Jimenez, Veronica ;
Otaegui, Pedro ;
Mulero, Francisca ;
Navarro, Marc ;
Ruberte, Jesus ;
Bosch, Fatima .
NATURE COMMUNICATIONS, 2021, 12 (01)
[38]   AAV-Mediated Gene Supply for Treatment of Degenerative and Neovascular Retinal Diseases [J].
Colella, Pasqualina ;
Auricchio, Alberto .
CURRENT GENE THERAPY, 2010, 10 (05) :371-380
[39]   AAV-mediated gene transfer for the treatment of hemophilia B: problems and prospects [J].
N C Hasbrouck ;
K A High .
Gene Therapy, 2008, 15 :870-875
[40]   AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo [J].
Hung, Sandy S. C. ;
Chrysostomou, Vicki ;
Li, Fan ;
Lim, Jeremiah K. H. ;
Wang, Jiang-Hui ;
Powell, Joseph E. ;
Tu, Leilei ;
Daniszewski, Maciej ;
Lo, Camden ;
Wong, Raymond C. ;
Crowston, Jonathan G. ;
Pebay, Alice ;
King, Anna E. ;
Bui, Bang V. ;
Liu, Guei-Sheung ;
Hewitt, Alex W. .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57 (07) :3470-3476