New gene therapy can help people with spinal cord injuries to re-learn skilled hand movements.
New gene therapy can potentially help people with spinal cord injuries to re-learn skilled hand movements, reports a new study. The findings of the study are published in the journal Brain. People with spinal cord injury often lose the ability to perform everyday actions that require coordinated hand movements such as writing, holding a toothbrush or picking up a drink.
‘New gene therapy can restore hand function after spinal cord injury by causing cells to produce an enzyme called chondroitinase which can break down the scar tissue and allow networks of nerve cells to regenerate.’
In the study, the researchers tested the new gene therapy on rats for regenerating damaged tissue in the spinal cord that could be switched on and off using a common antibiotic."What is exciting about our approach is that we can precisely control how long the therapy is delivered by using a gene 'switch.' This means we can hone in on the optimal amount of time needed for recovery," said Elizabeth Bradbury, Professor at King's College London.
"Gene therapy provides a way of treating large areas of the spinal cord with only one injection, and with the switch, we can now turn the gene off when it is no longer needed," she added.
After a traumatic spinal injury, dense scar tissue forms which prevent new connections being made between nerve cells.
The gene therapy causes cells to produce an enzyme called chondroitinase which can break down the scar tissue and allow networks of nerve cells to regenerate.
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"We found that when the gene therapy was switched on for two months, the rats were able to accurately reach and grasp sugar pellets," explained Emily Burnside from King's College London.
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However, the researchers had to overcome a problem with the immune system recognizing and removing the gene switch mechanism.
To get around this, they added a "stealth gene" which hides the gene switch from the immune system.
The gene therapy is not yet ready for human trials, the researchers said.
Source-IANS