Prime editing treats childhood brain disease in mice

(Press-News.org) Prime editing treats childhood brain disease in mice

Scientists use a precise form of gene editing called prime editing to correct the most common genetic mutations that cause alternating hemiplegia of childhood, a rare and severe neurological disorder that begins in infancy.

 

July 21, 2025 (Cambridge, MA) — By the time they are a few months old, infants born with alternating hemiplegia of childhood (AHC) begin experiencing terrifying episodes of paralysis and seizures, and will soon show developmental delays and intellectual disability. There is no cure or effective treatment for this rare genetic disease, but new research suggests a potential path to one.

Researchers at the Broad Institute and The Jackson Laboratory have used prime editing, a precise and versatile form of gene editing, to correct the root cause of AHC in mice. The team used a scalable approach to develop prime editing treatments that directly repaired five different AHC-causing genetic mutations. Mice that received the treatment had far fewer and less severe symptoms of AHC, and survived more than twice as long as untreated mice.

The new study, published in Cell, is the first time prime editing has been used to treat a neurological disease in animals, offering hope for treating people with AHC and other genetic brain disorders. Prime editing was developed in 2019 by the lab of David Liu, a Broad core institute member and co-senior author of the new paper. The technology has already been successfully tested in a clinical trial for another rare genetic disease.

“This study is an important milestone for prime editing and one of the most exciting examples of therapeutic gene editing to come from our team,” said Liu, Richard Merkin Professor and director of the Merkin Institute of Transformative Technologies in Healthcare at the Broad. “It opens the door to one day repairing the underlying genetic causes of many neurological disorders that have long been considered untreatable.” Liu is also a Howard Hughes Medical Institute investigator and a professor at Harvard University.

The ability to precisely edit DNA directly in the brain has important implications for neurological diseases, said Cathleen Lutz, vice president of the Rare Disease Translational Center at The Jackson Laboratory and co-senior author of the study. “This level of editing efficiency in the brain is really quite remarkable.”

The team’s patient partner is RARE Hope (formerly Hope for Annabel), a non-profit focused on accelerating research on AHC and developing scalable, patient-centric research platforms to benefit the larger rare disease community. RARE Hope initiated the collaboration and was closely engaged throughout the project.

“This study is a win not just for our community but for all rare neurological conditions, and a breakthrough moment in expanding access to a broader cohort of potential patients,” said Nina Frost, founder and president of RARE Hope, a co-author of the study, and mother of a daughter with AHC. “It’s been a privilege to collaborate on such a scientifically significant effort with a team that has kept patients at the center of proof-of-concept research — engaging the patient community, modeling the patient experience, and integrating patient priorities into experimental design. This is a model for patient-relevant, patient-centered research because the team included us as true partners.”

Brain gene editing

The vast majority of AHC cases are caused by one of four mutations in ATP1A3, a gene essential for brain cell function. In the new work, Liu’s team set out to simultaneously develop prime editing treatments that could fix five ATP1A3 mutations, including the four most common — a scale rarely attempted in therapeutic gene editing research. Most other gene editing treatments, such as one recently used to treat baby KJ Muldoon, are designed to correct one mutation at a time. The scientists worked on correcting all five mutations, streamlining experiments, saving resources, and testing the robustness of the underlying science.

“We developed a robust framework to correct multiple mutations in parallel,” said Alexander Sousa, a postdoctoral fellow in the Liu lab and one of three co-first authors along with Holt Sakai of the Liu lab and Markus Terrey of The Jackson Laboratory. “This effort was really about creating a blueprint that could be rapidly applied to other rare diseases too.”

The researchers first tested their strategies in cultured cells from patients with AHC. They demonstrated that they could correctly repair AHC mutations in up to 90 percent of treated cells, with minimal changes to other stretches of DNA.

Next, the group collaborated with Jackson Lab researchers to test their treatments in two mouse models of AHC, which carry Atp1a3 mutations similar to those in patients with AHC. Without treatment, the mice developed seizures, movement problems, and died prematurely. When the scientists injected their editing system into the brains of the animals, their symptoms disappeared or were substantially reduced. Treated mice survived more than twice as long as untreated animals. Moreover, the function of their Atp1a3 protein was restored in the brain, and their motor and cognitive deficits were ameliorated. The scientists delivered the prime editors to cells in mice using clinically validated viruses called AAVs, which are already used in FDA-approved gene therapies targeting brain cells.

“The results really exceeded our expectations,” said Sakai. “It was incredibly exciting to see that data.”

The team also tested traditional gene therapy, which delivered an extra, healthy copy of the ATP1A3 gene to cells, and found that symptoms did not improve in animals. This finding highlights the unique advantage of using gene editing to directly correct a mutation that results in a malfunctioning, disease-causing protein, the researchers said.

“Before this study, we didn’t even know if we could intervene in AHC after birth in an animal,” said Sousa. “Now we know you can.”

A template for rare diseases

Because the treatment required direct injection into the brain shortly after birth, the team is now exploring less invasive delivery methods, and whether treatment later in life could still be effective.

Beyond AHC, the team sees their approach as a template for tackling other rare genetic diseases — especially those that affect the brain. With the ability to rapidly design and test multiple gene editing treatments at once, they hope to bring the same precision and speed to many other conditions.

“This is a powerful proof of concept,” said Sakai. “It shows that we can use prime editing to treat genetic brain diseases, and it lays the groundwork for translating this approach to the clinic.”

 

Support for the study was provided by the National Institutes of Health, the Chan-Zuckerberg Initiative, RARE Hope, the Alternating Hemiplegia of Childhood Foundation, the For Henry AHC Foundation, the Davis Family Foundation, the Toolbox Foundation L2C Initiative, the Cure AHC Foundation, the Howard Hughes Medical Institute, and the National Science Foundation.

Paper(s) cited:

Sousa AA, Terrey M, Sakai HA et al. In vivo prime editing rescues alternating hemiplegia of childhood in mice. Cell. Online July 21, 2025. DOI: TK

 

About the Broad Institute

The Broad Institute is an independent, non-profit research organization whose mission is to understand the roots of disease and close the gap between new biological insights and impact for patients.

Founded in 2004 by the visionary Los Angeles philanthropists Eli and Edythe Broad, the Broad Institute exists at the intersection of scientific disciplines, convening scientists and other experts from genomics, cell biology, chemistry, engineering, neuroscience, therapeutics, artificial intelligence/machine learning, computational biology, and public health. The Broad Institute engages thousands of scientists from MIT, Harvard, Harvard’s primary teaching hospitals, academic institutions, and leading corporate partners from the pharmaceutical and biotechnology industries, all who share the goal of translating research findings into safe and effective therapeutic interventions for all common and rare diseases.

 

 

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