“This is the first time someone could have a new gene put into their liver,” Sangamo President and CEO Sandy Macrae told The Scientist in May. “It’s a privilege and a responsibility to do” these trials.
“It’s kind of humbling,” Madeux tells the Associated Press about being the first to receive such an in vivo gene-editing treatment. “I’m willing to take that risk. Hopefully it will help me and other people.”
Hunter syndrome is a rare condition in which people lack an enzyme that breaks down complex polysaccharides. To correct it, ZFNs are directed to cut the gene for albumin in liver cells, where the functional copy of the enzyme’s gene is then incorporated. The therapy was developed by California-based Sangamo Therapeutics.
Compared to genome editing based on CRISPR-Cas9, “zinc finger nucleases are a little more cumbersome to develop,” Paula Cannon of the University of Southern California’s Keck School of Medicine told The Scientist in May. But they offer superior specificity, she said. Sangamo’s system “gives you very specific and highly effective zinc finger nucleases,” said Cannon, who was not involved in the trial. “They can target ZFNs to cut at any particular base.”
Sangamo is also looking to begin treating hemophilia B and Hurler syndrome using ZFNs.