Editing of genes inside patient a world first
UNITED STATES: Doctors have edited a patient’s genes in a world-first attempt to alter DNA from within the human body.
The doctors in California administered the experimental intravenous treatment, which provides the body with instructions to change DNA, on Brian Madeux, who suffers from Hunter’s syndrome.
People with Hunter’s syndrome are unable to break down long, sugary molecules called mucopolysaccharides. This leads to the molecules building up and causing brain and organ damage, and in severe cases it can be fatal.
Sufferers require regular enzyme replacement therapy, but Madeux said he opted to take part in the California trial because he was ‘‘in pain every second of the day’’.
The 44-year-old from Arizona underwent the treatment at UCSF Benioff Children’s Hospital in Oakland on Tuesday. It is too soon to know whether the pioneering procedure has worked, but if successful, his DNA will now have the instructions for making the enzyme.
Madeux intravenously received billions of copies of a corrective gene and genetic tools to cut his DNA in a precise spot. They travel to the liver, where cells use the instructions to make molecular ‘‘scissors’’ and prepare the corrective gene. The DNA is cut, allowing the new gene to slip in. The new gene then directs the cell to make the enzyme the patient lacked.
‘‘We cut your DNA, open it up, insert a gene, stitch it back up,’’ said Dr Sandy Macrae, president of Sangamo Therapeutics, the Californian company testing the technique for two metabolic diseases and haemophilia. ‘‘It becomes part of your DNA and is there for the rest of your life.’’
The technique has been carried out before, but previous procedures have involved cells being taken out of the body to be edited before being returned. This is impossible to do with cells within organs like the liver, heart or brain.
Madeux’s procedure was attempted to test the safety of performing the gene editing before further research into administering the therapy. If he continues to do well, a further nine patients will receive the procedure.
Dr David R Liu, from Harvard University, said: ‘‘The Hunter syndrome trial, led by a pioneering company, is another reminder that we have entered an era of genome editing.’’
But Dr Robin Lovell-badge, from the Francis Crick Institute, said there were challenges ahead in developing the treatment. ‘‘Taking it to more complex things like muscular dystrophy and cystic fibrosis will require a lot more work.’’
– Telegraph Group