{"id":4026,"date":"2025-10-07T11:58:49","date_gmt":"2025-10-07T10:58:49","guid":{"rendered":"https:\/\/sites.manchester.ac.uk\/lydia-becker-institute\/?p=4026"},"modified":"2025-10-07T12:09:36","modified_gmt":"2025-10-07T11:09:36","slug":"nobel-prize-2025-regulatory-t-cells-tracy-hussell","status":"publish","type":"post","link":"https:\/\/sites.manchester.ac.uk\/lydia-becker-institute\/2025\/10\/07\/nobel-prize-2025-regulatory-t-cells-tracy-hussell\/","title":{"rendered":"Nobel prize awarded for discovery of immune system\u2019s \u2018security guards\u2019"},"content":{"rendered":"

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In this piece originally published in The Conversation<\/a>, Lydia Becker Institute Director Professor Tracy Hussell<\/a> breaks down the science behind this year\u2019s Nobel Prize in Medicine.\u00a0She explains how three scientists, Shimon Sakaguchi, Mary E. Brunkow, and Fred Ramsdell, discovered the immune system\u2019s very own \u201csecurity guards\u201d: regulatory T cells. These tiny peacekeepers stop our immune system from turning on itself, a discovery that\u2019s changing how we understand \u2014 and treat \u2014 autoimmune diseases, inflammation, and even cancer.<\/strong><\/em><\/p>\n

Three scientists have been awarded the 2025 Nobel prize in physiology or medicine for discovering how the body stops its own immune system from turning against itself.<\/p>\n

Shimon Sakaguchi from Osaka University in Japan, Mary E. Brunkow from the Institute for System Biology and Fred Ramsdell from Sonoma Biotherapeutics, both in the USA, identified specialised \u201csecurity guard\u201d cells that keep our immune system in check.\u00a0These discoveries<\/a>\u00a0have been important for understanding how to treat and prevent autoimmune conditions. The trio will share a prize sum of 11 million Swedish Kronor (\u00a3870,000).<\/p>\n

An effective immune system is critical. It sculpts tissues as they grow and clears away old cells and debris. It also eliminates dangerous viruses, bacteria and fungi, keeping us healthy.<\/p>\n

But the immune system faces a delicate challenge: it must attack thousands of different invading microbes each day, many of which have evolved to look remarkably similar to our own cells \u2013 yet it must never mistake our own tissue for the enemy.<\/p>\n

So how does the immune system know what cells it should attack and which ones it shouldn\u2019t?<\/p>\n

This question has been studied by immunologists for decades. But it was the groundbreaking work by this year\u2019s Nobel laureates that led to the discovery of the specialised immune cells \u2013 called regulatory T cells \u2013 which prevent immune cells from attacking our own body and keep the immune system running as it should.<\/p>\n

For decades, immunologists weren\u2019t certain why some immune cells functioned as they should, and why others went rogue and attacked the body\u2019s own tissues. When this happens, it can result in autoimmune conditions \u2013 such as type 1 diabetes, rheumatoid arthritis and multiple sclerosis.<\/p>\n

For a long time, scientists believed the thymus \u2013 a small gland in the chest \u2013 was solely responsible for immune tolerance. Immune cells (specifically a type of cell called a T lymphocyte) that recognised the body\u2019s own proteins too strongly were initially thought to be eliminated in the thymus in early life. Those immune cells that only showed mild reactivity were then released into the bloodstream to patrol the body.<\/p>\n

But work conducted in the 1980s and 1990s by Sakaguchi showed that there was a specialised class of immune T cells that played a critical role in suppressing immune responses and preventing the immune system from attacking the body\u2019s tissues.<\/p>\n

In Sakaguchi\u2019s first experiment, he surgically removed the thymus organ from newborn mice, then injected T cells into them from genetically similar mice. He hypothesised that the mice would have a weaker immune system and develop fewer T cells.<\/p>\n

Instead, he discovered that there appeared to be T cells that protected the mice from developing autoimmune diseases.<\/p>\n

Over the next decade, Sakaguchi set out to uncover whether there were different types of T cells that played different roles in immune response. In 1995, Sakaguchi\u00a0published the paper<\/a>\u00a0that detailed a new class of T cell, called a \u201cregulatory T cell\u201d. It showed that T cells carrying a specific type of protein on their surface actually eliminated harmful T cells.<\/p>\n

There was initial scepticism among scientists about the existence of regulatory T cells. But work from Brunkow and Ramsdell published in the 1990s and early 2000s showed how regulatory T cells work.<\/p>\n

Brunkow and Ramsdell\u2019s research showed that\u00a0regulatory T cells<\/a>\u00a0prevent immune cells from attacking the body by secreting immune dampening proteins or by directly delivering anti-inflammatory signals.<\/p>\n

They also discovered a\u00a0specific protein<\/a>\u00a0that identified these regulatory T cells (called FoxP3). This meant scientists could work out when a cell was regulatory and also isolate them for study.<\/p>\n

These discoveries showed how important regulatory T cells (also called T-regs for short) are in regulating other inflammatory immune cells in the body.<\/p>\n

The work of this year\u2019s Nobel laureates has also massively opened up the field of immunology, going far beyond merely understanding the process of immune tolerance.<\/p>\n

Their work has revealed that immunity and inflammation is actively regulated. It has provided a raft of new ideas to control inflammatory disease, whether caused by infection, allergens, environmental pollutants or autoimmunity.<\/p>\n

It has even provided new ideas to prevent rejection of transplants and has opened up new ways of improving immune responses to cancer treatments and vaccines.<\/p>\n