Advances in gene therapy hold promise for treating hereditary hearing loss

L Jiang, D Wang, Y He, Y Shu - Molecular Therapy, 2023 - cell.com
Gene therapy focuses on genetic modification to produce therapeutic effects or treat
diseases by repairing or reconstructing genetic material, thus being expected to be the most …

Gene therapy for hearing loss

R Omichi, SB Shibata, CC Morton… - Human molecular …, 2019 - academic.oup.com
Sensorineural hearing loss (SNHL) is the most common sensory disorder. Its underlying
etiologies include a broad spectrum of genetic and environmental factors that can lead to …

Cochlear gene therapy with ancestral AAV in adult mice: complete transduction of inner hair cells without cochlear dysfunction

J Suzuki, K Hashimoto, R Xiao, LH Vandenberghe… - Scientific reports, 2017 - nature.com
The use of viral vectors for inner ear gene therapy is receiving increased attention for
treatment of genetic hearing disorders. Most animal studies to date have injected viral …

Gene therapy restores balance and auditory functions in a mouse model of Usher syndrome

K Isgrig, JW Shteamer, IA Belyantseva, MC Drummond… - Molecular therapy, 2017 - cell.com
Dizziness and hearing loss are among the most common disabilities. Many forms of
hereditary balance and hearing disorders are caused by abnormal development of …

Emerging approaches for restoration of hearing and vision

S Kleinlogel, C Vogl, M Jeschke, J Neef… - Physiological …, 2020 - journals.physiology.org
Impairments of vision and hearing are highly prevalent conditions limiting the quality of life
and presenting a major socioeconomic burden. For a long time, retinal and cochlear …

Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation

H Yoshimura, SB Shibata, PT Ranum, RJH Smith - Scientific reports, 2018 - nature.com
Cochlear gene therapy holds promise for the treatment of genetic deafness. Assessing its
impact in adult murine models of hearing loss, however, has been hampered by technical …

New molecular therapies for the treatment of hearing loss

Y Ma, AK Wise, RK Shepherd… - Pharmacology & …, 2019 - Elsevier
An estimated 466 million people suffer from hearing loss worldwide. Sensorineural hearing
loss is characterized by degeneration of key structures of the sensory pathway in the …

Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice

Q Yu, Y Wang, Q Chang, J Wang, S Gong, H Li, X Lin - Gene therapy, 2014 - nature.com
Mutations in GJB2, which codes for the gap junction (GJ) protein connexin26 (Cx26), are the
most common causes of human nonsyndromic hereditary deafness. We inoculated modified …

Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange‐Nielsen deafness …

Q Chang, J Wang, Q Li, Y Kim, B Zhou… - EMBO molecular …, 2015 - embopress.org
Mutations in the potassium channel subunit KCNQ 1 cause the human severe congenital
deafness Jervell and Lange‐Nielsen (JLN) syndrome. We applied a gene therapy approach …

Delivery of adeno-associated virus vectors in adult mammalian inner-ear cell subtypes without auditory dysfunction

Y Tao, M Huang, Y Shu, A Ruprecht, H Wang… - Human gene …, 2018 - liebertpub.com
Hearing loss, including genetic hearing loss, is one of the most common forms of sensory
deficits in humans with limited options of treatment. Adeno-associated virus (AAV)-mediated …