Cookies

Like most websites The Translational Scientist uses cookies. In order to deliver a personalized, responsive service and to improve the site, we remember and store information about how you use it. Learn more.
Research Field Cell & gene therapy

Perusing the Pipeline

Preclinical

Scientists have developed a gene therapy that prevents axon destruction in mice. When an axon is damaged, either through injury or by certain therapeutic drugs, a protein called SARM1 becomes active, which triggers axons to self-destruct. This destruction likely plays an important role in multiple neurodegenerative conditions, including peripheral neuropathy, Parkinson's disease and amyotrophic lateral sclerosis. The researchers used an AAV vector to introduce point mutations into human SARM1 and inhibit its function. They found axon preservation similar to that observed in SARM1 knockout mice (1).

An international team of researchers have used gene therapy to restore hearing in an adult mouse model of DFNB9 deafness – a hearing disorder that represents one of the most frequent cases of congenital genetic deafness in humans. Individuals with DFNB9 deafness are deficient in the gene coding for otoferlin, a protein essential for transmitting sound information at auditory sensory cell synapses. The researchers used a single intracochlear injection of two different recombinant AAV vectors to reconstruct the otoferlin coding region, leading to long-term restoration of otoferlin expression in the inner hair cells, and restored hearing (2).

Read the full article now

Log in or register to read this article in full and gain access to The Translational Scientist’s entire content archive. It’s FREE and always will be!

Login

Or register now - it’s free and always will be!

You will benefit from:

  • Unlimited access to ALL articles
  • News, interviews & opinions from leading industry experts
Register

Or Login via Social Media

By clicking on any of the above social media links, you are agreeing to our Privacy Notice.

About the Author

James Strachan

Over the course of my Biomedical Sciences degree it dawned on me that my goal of becoming a scientist didn’t quite mesh with my lack of affinity for lab work. Thinking on my decision to pursue biology rather than English at age 15 – despite an aptitude for the latter – I realized that science writing was a way to combine what I loved with what I was good at.
From there I set out to gather as much freelancing experience as I could, spending 2 years developing scientific content for International Innovation, before completing an MSc in Science Communication. After gaining invaluable experience in supporting the communications efforts of CERN and IN-PART, I joined Texere – where I am focused on producing consistently engaging, cutting-edge and innovative content for our specialist audiences around the world.

Register to The Translational Scientist

Register to access our FREE online portfolio, request the magazine in print and manage your preferences.

You will benefit from:

  • Unlimited access to ALL articles
  • News, interviews & opinions from leading industry experts

Register