Gene therapy beneficial for deadly childhood liver disease: Study
A new gene therapy has been used to successfully treat a deadly childhood liver disease using mice that model this disease by researchers at UCL and Great Ormond Street Hospital.
Arthrogryposis, Renal dysfunction and Cholestasis (ARC) syndrome is a lethal genetic disorder usually caused by a lack of the VPS33B protein with children diagnosed with the condition rarely living beyond their first year of life.
Now, in a study published in Nature Communications, the UCL-GOSH team has found that by injecting a healthy version of the gene in the body they can treat this condition in mice lacking VPS33B.
Crucially, the final version of the treatment, which specifically targeted the liver cells, caused no harm – in the earlier versions the genes became abnormally activated and caused cancerous cells to grow and expand in some cases.
While more tests need to be done before the treatment can be tested in humans, the researchers’ breakthrough offers hope to babies with this devastating disorder and their families. In the UK, as many as six pregnancies per year might be affected by ARC syndrome. Furthermore, it may allow better understanding of why some treatments may cause cancer.
Lead author Dr Claudiu Cozmescu (UCL Great Ormond Street Institute of Child Health) said: “Our findings are important because it provides proof-of-concept that gene therapy could become a realistic treatment for ARC syndrome and potentially other inherited liver diseases that currently have few or no effective options.
“It also highlights that how a gene therapy is designed is critical: targeting treatment specifically to the liver improved safety while maintaining benefit.
“The findings should be of interest to patients and families affected by rare liver diseases, clinicians, gene therapy researchers, biotech developers, regulators, and charities supporting rare disease research.
“Before human trials, further long-term toxicology and safety studies will be needed.”
ARC syndrome is a medical condition where the flow of bile from your liver is reduced or completely blocked. Bile is a digestive fluid produced by the liver to break down fats. When its flow is stalled, bile components (like bilirubin and bile acids) build up in the liver and leak into the bloodstream, leading to sepsis which is usually fatal.
For the trial the scientists used special mice that had been genetically engineered so that the VPS33B gene did not work properly.
Some mice had no working copy of the gene in their liver (the “disease” mice) while others had only one working copy (which were used for safety testing).
Because of this missing or faulty gene, the mice developed liver problems similar to those seen in children with ARC syndrome.
The researchers found that the treatment helped the mice’s livers start working properly again: the mice lived longer (about 80% survived compared with about 33% which did not have the treatment), and their livers had less scarring (fibrosis).
The treatment was more effective when given throughout the body rather than just targeting the liver.
However, in the initial attempts to cure the disease around 30% of those mice developed liver tumours – the risk of cancer developing as a side effect of gene therapy has been raised in previous trials.
But none of the mice treated with the final, liver-targeted version developed tumours, suggesting gene therapy can be safe if done correctly.
Reference:
Cozmescu, C.A., Nazari, M., Touramanidou, L. et al. Safety and efficacy analysis of in vivo lentiviral gene therapy in pre-clinical ARC syndrome models. Nat Commun 17, 5074 (2026). https://doi.org/10.1038/s41467-026-73631-x
