Emmanuel Mignot wins Breakthrough Prize for discovering cause of narcolepsy

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2022-09-23 17:00:32

“I think receiving this Breakthrough Prize is incredible, and I also definitely have the reward of seeing my patients completely changed by these new drugs,” said Emmanuel Mignot. “It’s a fantastic kind of human adventure.” Stanford Medicine photo Emmanuel Mignot, MD, PhD, the Craig Reynolds Professor of Sleep Medicine, is the winner of a 2023 Breakthrough Prize in Life Sciences. He will share the $3 million prize with Masashi Yanagisawa, MD, PhD, of the University of Tsukuba for discovering the causes of narcolepsy and paving the way for new treatments for sleep disorders.   “I became interested in narcolepsy because I thought it was a key to understanding sleep, and because it had this human dimension of trying to help patients with this disease that nobody cared about,” Mignot said. “When I started studying narcolepsy, people thought it was very rare. Nobody knew about it.” The Breakthrough Prize recognizes top scientists for their game-changing discoveries in the fields of life sciences, fundamental physics and mathematics. Nearly $16 million was awarded this year. “For so many years, the neurological mechanisms that cause narcolepsy were a complete mystery to the medical community,” said Lloyd Minor, MD, dean of the Stanford School of Medicine. “Dr. Mignot’s research not only unearthed the protein at the center of this mystery but also led to effective treatments and therapies for people suffering from the condition. Through his brilliant work, Dr. Mignot forever changed the field of sleep medicine and, in doing so, opened the door for more discoveries across a variety of neurodegenerative diseases.”  Hunting for a narcolepsy gene in dogs Mignot has dedicated his career to understanding and treating narcolepsy and other sleep disorders. Narcolepsy is a neurological disorder characterized by extreme sleepiness and rapid transition into REM sleep, the sleep phase in which dreams occur. People with narcolepsy contend with sudden bouts of sleepiness and muscle weakness, known as cataplexy, that can be triggered by strong emotional excitement. The disorder, which affects about 1 in 2,000 people, is usually diagnosed between childhood and young adulthood. “Through unflinching curiosity and persistence, Dr. Mignot and his colleagues led the way to a discovery that would change the lives of millions of people around the world struggling with narcolepsy’s terrible and unpredictable effects,” said Marc Tessier-Lavigne, president of Stanford University. “Groundbreaking, life-changing research like this is what we strive to enable every day at Stanford. I’m proud to congratulate Dr. Mignot, who so deeply deserves this recognition.” Mignot’s interest in studying narcolepsy began in 1986, when he convinced the French government that, as part of his mandatory military service, he should be sent to Stanford Medicine to study a drug for narcolepsy that had been developed by a French company. Working in the lab of the late William Dement, MD, PhD, who was known as the father of sleep medicine, Mignot studied the drug modafinil and showed that it worked in a manner similar to amphetamines by increasing dopamine levels in the brain. The experience convinced Mignot that narcolepsy was a tractable problem that could be understood and solved — he was hooked. Despite not having a faculty position or grants to support his work, he resigned from his professorship in France and continued his research at Stanford Medicine. In 1989, he embarked on a project to find the gene that causes narcolepsy in dogs. It was a bold approach at the time, one year before the Human Genome Project was even underway. “Probably it was a little bit of naivete because I was not a geneticist. I was trained as a psychiatrist, but I became a geneticist,” he said. “It took me 10 years to find the gene.” Emmanuel Mignot with his dog, Watson, who has narcolepsy, in 2016. Mignot sometimes takes Watson to the sleep clinic to help explain the disease to his younger patients. Photo by Lenny Gonzalez The gene turned out to control a receptor for a sleep-modulating neurotransmitter, commonly known today as orexin, that had been recently discovered by fellow Stanford Medicine sleep researcher, Luis de Lecea, PhD, and separately by Yanagisawa in Japan. Mignot published his findings, showing that narcolepsy was caused by the disruption of the orexin system in the brain in Cell in 1999. Around the same time, in parallel work in mice, Yanagisawa had come to the same conclusion. New treatments for narcolepsy in humans The next year, Mignot demonstrated that orexin, which promotes wakefulness and blocks REM sleep, was absent in the brains of human patients with narcolepsy. Further work from his lab would show that human narcolepsy is an autoimmune disorder in which some 70,000 orexin-producing neurons in the hypothalamus are destroyed by the body’s own immune system. (Mignot compared the biology of narcolepsy to that of Type I diabetes, in which the body’s immune system destroys insulin-producing cells in the pancreas.) His team has identified genetic factors that underlie human narcolepsy and the autoimmune processes, which can be triggered by certain influenza strains, that lead to orexin deficiency. The discovery of narcolepsy’s roots has led to the development of drugs that can prevent or promote sleepiness by targeting the orexin system. Mignot, who treats several hundred narcolepsy patients each year, is involved in several clinical trials of narcolepsy drugs that show promise in reducing symptoms. He is also investigating the role of autoimmunity in other neurodegenerative disorders, such as Alzheimer’s and Parkinson’s diseases. “I think receiving this Breakthrough Prize is incredible, and I also definitely have the reward of seeing my patients completely changed by these new drugs,” said Mignot. “It’s a fantastic kind of human adventure.” Mignot joined the Stanford Medicine faculty in 1993, when he also was named director of the Stanford Medicine Center for Narcolepsy. He is a member of the National Academy of Sciences and the National Academy of Medicine and has received numerous awards for his pioneering work. Mignot joins developmental biologist Roeland Nusse, PhD, and psychiatrist and neuroscientist Karl Deisseroth, MD, PhD, as prior Stanford Medicine winners of the Breakthrough Prize. The Breakthrough Prizes were founded by Sergey Brin, Priscilla Chan and Mark Zuckerberg, Julia and Yuri Milner and Anne Wojcicki. They have been sponsored by foundations established by them. Selection committees composed of previous Breakthrough Prize laureates in each field choose the winners.

“I think receiving this Breakthrough Prize is incredible, and I also definitely have the reward of seeing my patients completely changed by these new drugs,” said Emmanuel Mignot. “It’s a fantastic kind of human adventure.” Stanford Medicine photo

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