Researchers develop treatment for rare, genetic liver disease

liver disease
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Researchers at Saint Louis University's School of Medicine, in collaboration with Arrowhead Pharmaceuticals and Takeda Pharmaceuticals, report the first effective drug to treat a rare, genetic liver disease that formerly could only be treated with a liver transplant.

The study, "Fazirsiran for Liver Disease Associated with Alpha1-Antitrypsin Deficiency," was published online in the New England Journal of Medicine.

The multicenter, phase 2, open-label trial investigated the safety and efficacy of fazirsiran, an RNA interference drug, in patients 18 to 75 years of age with liver disease associated with alpha-1 antitrypsin (AAT) deficiency. AAT is a protein made in the liver and released into the blood in large quantities to help protect the body when warding off infections.

Jeffrey Teckman, M.D., professor of pediatrics and biochemistry and molecular biology, is the paper's senior author.

"This is the culmination of over a decade of work to cure this disease, and a significant part of the work was done here," said Teckman, who also is director of pediatric gastroenterology and hepatology at SLU. "We have patients come around the country to see SLU's expert faculty members at SSM Health Cardinal Glennon Children's Hospital with this disease for care and to participate in our studies."

Teckman is a leading authority on AAT deficiency, which affects 1 in 3,500 births and causes severe lung disease in adults or liver disease in adults and children. Symptoms may include shortness of breath and wheezing, repeated infections of the lungs, yellow skin, fatigue, cirrhosis of the liver, and even death.

Teckman says those impacted by the disease are often undiagnosed or misdiagnosed as fatty , asthma, or smoking-related lung disease. The diagnosis may be suspected by finding low levels of AAT in the blood and confirmed by genetic testing.

"When I was in , I learned that reduction in liver fibrosis, or in the liver, with AAT deficiency was impossible, but now we see that we can reverse this process in humans with minimal side effects," Teckman said.

Longtime collaborator Arrowhead Pharmaceuticals utilized technology during the trial, allowing physicians to shut down one gene in the human liver with almost no side effects.

"In this case, we chose to shut down the abnormal alpha-1 antitrypsin gene in the liver, and the new drug can do that effectively, stopping the disease and allowing the liver to heal," Teckman said.

Next, the team will expand the international study to additional adult patients and children in collaboration with Takeda Pharmaceuticals.

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More information: Pavel Strnad et al, Fazirsiran for Liver Disease Associated with Alpha1-Antitrypsin Deficiency, New England Journal of Medicine (2022). DOI: 10.1056/NEJMoa2205416
Journal information: New England Journal of Medicine

Citation: Researchers develop treatment for rare, genetic liver disease (2022, July 11) retrieved 25 September 2022 from
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