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Gene therapy for rare epilepsy shows promise in mice

Findings are proof-of-concept for an innovative approach

Date:
February 14, 2025
Source:
Michigan Medicine - University of Michigan
Summary:
Recent research takes aim at the a variant in gene SCN1B, which causes a severe form of developmental epileptic encephalopathy.
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FULL STORY

Dravet syndrome and other developmental epileptic encephalopathies are rare but devastating conditions that cause a host of symptoms in children, including seizures, intellectual disability, and even sudden death.

Most cases are caused by a genetic mutation; Dravet syndrome in particular is most often caused by variants in the sodium channel gene SCN1A.

Recent research from Michigan Medicine takes aim at another variant in SCN1B, which causes an even more severe form of DEE.

Mice without the SCN1B gene experience seizures and 100 percent mortality just three weeks after birth.

Using mouse models, the investigative team, led by Chunling Chen, M.D., and Yukun Yuan, M.D., Ph.D., in the lab of Lori Isom, Ph.D., of the Department of Pharmacology at the Medical School, tested a gene therapy to replace SCN1B to increase the expression of beta-1 protein, which is necessary for the regulation of sodium channels in the brain.

Administering the therapy to newborn mice increased their survival, reduced the severity of their seizures and restored brain neuron excitability.

The team notes that different forms of SCN1B gene expression may result in different outcomes for the therapy.

However, the proof-of-concept is the first step toward a gene replacement therapy for SCN1B-linked developmental and epileptic encephalopathy.


Story Source:

Materials provided by Michigan Medicine - University of Michigan. Original written by Kelly Malcom. Note: Content may be edited for style and length.


Journal Reference:

  1. Chunling Chen, Yukun Yuan, Heather A. O'Malley, Robert Duba-Kiss, Yan Chen, Karl Habig, Yosuke Niibori, Samantha L. Hodges, David R. Hampson, Lori L. Isom. Neonatal but not Juvenile Gene Therapy Reduces Seizures and Prolongs Lifespan in SCN1B-Dravet Syndrome Mice. Journal of Clinical Investigation, 2025; DOI: 10.1172/JCI182584

Cite This Page:

Michigan Medicine - University of Michigan. "Gene therapy for rare epilepsy shows promise in mice." ScienceDaily. ScienceDaily, 14 February 2025. <www.sciencedaily.com/releases/2025/02/250214133100.htm>.
Michigan Medicine - University of Michigan. (2025, February 14). Gene therapy for rare epilepsy shows promise in mice. ScienceDaily. Retrieved February 19, 2025 from www.sciencedaily.com/releases/2025/02/250214133100.htm
Michigan Medicine - University of Michigan. "Gene therapy for rare epilepsy shows promise in mice." ScienceDaily. www.sciencedaily.com/releases/2025/02/250214133100.htm (accessed February 19, 2025).

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