Nobel Prize in medicine to Brunkow, Ramsdell and Sakaguchi for studies on the immune system
Their research, fundamental to the treatment of cancer and autoimmune diseases, paves the way for new therapies now in clinical trials.
Key points
The 2025 Nobel Prize in Medicine was awarded to Mary E. Brunkow, Fred Ramsdell and Shimon Sakaguchi for their discoveries on the mechanisms of peripheral immune tolerance, a regulatory system that prevents the immune system from turning its weapons against the organism it is supposed to defend.
The research of the three scientists - two Americans and one Japanese - led to the identification of regulatory T-cells, true 'security guards' of the immune system. These cells act as sentinels that keep other immune cells at bay, preventing them from attacking healthy tissue. "Their discoveries have been decisive in understanding how the immune system works and why we do not all develop severe autoimmune diseases," said Olle Kämpe, chairman of the Nobel Committee.
A discovery that changed modern medicine
.It all began in 1995, when Professor Shimon Sakaguchi of Osaka University, going against prevailing theories, demonstrated that immunological tolerance is not only based on the elimination of 'dangerous' cells in the thymus (so-called central tolerance), but also on a peripheral control mechanism. Sakaguchi identifies for the first time a population of T-cells with a suppressive function, capable of maintaining peace in the immune system.
If the body's defence system is an army, the regulatory T-cells are its military police: they control that the soldiers do not rebel and destroy their own bases.
In 2001 came the contributions of Mary Brunkow and Fred Ramsdell, who discovered the FOXP3 gene, responsible for the development and functioning of these cells. Studying mice suffering from serious autoimmune diseases, the two researchers show that a mutation in this gene leads to a collapse of the control system, paving the way for the organism's self-destruction. The same mutation, in humans, causes a rare and devastating childhood disease, the IPEX syndrome.


