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Honoring the 2025 Nobel Laureates

October 6, 2025

By Ian Evans

Image of Nobel Model Clement morin

Pictured above: The medals and diplomas are prepared and packed at the Nobel Foundation to be sent to the home countries of the Nobel laureates. (© Nobel Prize Outreach. Photo: Clément Morin)

Read research from the 2025 Nobel Prize winners

Editor's note: This article will be continually updated with information about the newly announced Nobel Prize winners and access to their research.

In the coming days, the 2025 Nobel Laureates will be recognized for their significant contributions to science. That recognition reflects years of dedicated research that helps advance human progress for all.

The achievements of this year’s Laureates highlight the importance of rigorous, reproducible, and transparent research. Their work expands the boundaries of knowledge and sets a standard for scientific integrity, ensuring that the generations of researchers who follow them can build their own discoveries on the most reliable foundations.

Most importantly, all these researchers are part of a global community that collaborates across disciplines and borders to address complex challenges. By upholding high standards of transparency and accountability, they help maintain trust in the scientific process and inspire the next generation of scientists.

We congratulate the 2025 Nobel Laureates and celebrate their commitment to advancing science for the benefit of all.

The 2025 Nobel Prize in Physiology or Medicine has been awarded to Mary E. Brunkow (Institute for Systems Biology, Seattle), Fred Ramsdell (Sonoma Biotherapeutics, San Francisco), and Shimon Sakaguchi (Osaka University, Japan) for their discoveries concerning peripheral immune tolerance.

This year’s Nobel Laureates have fundamentally advanced our understanding of how the immune system distinguishes between harmful invaders and the body’s own tissues. Their research revealed the critical role of regulatory T cells—immune cells that act as “security guards,” preventing the immune system from attacking healthy organs. It's a discovery that has reshaped the field of immunology and opened new avenues for treating autoimmune diseases, cancer, and improving transplantation outcomes.

Shimon Sakaguchi’s pioneering work in 1995 challenged prevailing theories by identifying a previously unknown class of immune cells responsible for protecting the body from autoimmune diseases. Until then, it was widely believed that immune tolerance was solely established in the thymus through the elimination of harmful cells. Sakaguchi’s findings demonstrated that the immune system’s regulation is more complex, involving peripheral mechanisms. Shimon Sakaguchi is currently an advisory board member of the Cell Press journal Immunity.

Building on this, Mary Brunkow and Fred Ramsdell discovered in 2001 that mutations in the Foxp3 gene lead to severe autoimmune disorders in both mice and humans. Their work provided a genetic explanation for immune tolerance and linked Foxp3 to the development of regulatory T cells.

Sakaguchi later connected these discoveries, showing that Foxp3 is essential for the formation of regulatory T cells. Together, these breakthroughs have launched the field of peripheral tolerance and inspired new therapies, some of which are now in clinical trials.

Selected research by Physiology or Medicine Laureates

Mary E. Brunkow Disruption of Fnip1 Reveals a Metabolic Checkpoint Controlling B Lymphocyte Development

Proto-oncogenes in mammalian development

Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein

Polymorphisms in the Sclerosteosis/van Buchem Disease Gene (SOST ) Region Are Associated with Bone-Mineral Density in Elderly Whites

Frederick Ramsdell

Foxp3 and Natural Regulatory T Cells: Key to a Cell Lineage?

Fas and FasL in the homeostatic regulation of immune responses

Key Parameters of Tumor Epitope Immunogenicity Revealed Through a Consortium Approach Improve Neoantigen Prediction

Generation of lymphokine-activated killer cell activity from non-NK precursor cells

Second generation CD2-targeting LFA-3 fusion protein SBT115301 to restore immune homeostasis in autoimmune disease

Shimon Sakaguchi

Soluble CTLA-4 regulates immune homeostasis and promotes resolution of inflammation by suppressing type 1 but allowing type 2 immunity

Neoself-antigens are the primary target for autoreactive T cells in human lupus

Natural regulatory T cells: mechanisms of suppression

FOXP3+ regulatory T cells: control of FOXP3 expression by pharmacological agents

Thymically imprinted heterogeneity results in differential Treg induction and stability of effector identity

Transcription factor Ikzf1 associates with Foxp3 to repress gene expression in Treg cells and limit autoimmunity and anti-tumor immunity

Single-cell transcriptome landscape of circulating CD4 + T cell populations in autoimmune diseases

The dichotomous role of IL-2: tolerance versus immunity

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Ian Evans

Content Director

Elsevier

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