About the Center

Type 1 diabetes (T1D) is caused by the destruction of insulin-producing beta cells in the pancreas by the immune system. The breakdown of immune tolerance—the ability to distinguish between “self” and “non-self”—is central to autoimmunity and T1D pathology. Understanding the interactions between immune cells and beta cells may uncover clues about how to restore immune tolerance and stop beta cells from being destroyed.

The Center of Excellence in Northern California is bringing together scientific and clinical teams from Stanford University and the University of California, San Francisco (UCSF) to drive research into therapies that can restore balance to the immune system in T1D. By combining expertise in immunology, transplantation, beta cell biology, vascularization, biomaterial science, and cell engineering, the Center aims to answer unresolved questions that individual projects could not, most importantly focusing on the autoimmune attack on beta cells and figure out new ways to reset and control the immune system.

This knowledge will be used to address one of the biggest challenges in T1D research: developing approaches to allow for successful beta cell replacement without the need for broad immunosuppression. The multidisciplinary teams collaborating across each institution will develop new technologies and therapies to protect transplanted cells from immune rejection so they can survive and make insulin.

This Center is a cures accelerator and a high-impact partnership supported by Breakthrough T1D, maximizing resources, expertise, and data to accomplish our shared goals. By combining scientific expertise from each institution and capitalizing on the diverse and complementary skillsets of the investigators, this Center will drive research into new curative therapies for T1D.

These world-class researchers will:

  • Investigate the underlying mechanisms of autoimmunity in T1D
  • Validate new and available immunotherapies and cell engineering technologies that can protect transplanted islets from rejection by restoring balance to the immune system
  • Improve function and survival of manufactured islets post-transplant by providing an optimal environment that includes biomaterial-based scaffolds and new ways to increase blood flow and supply of nutrients and oxygen to cells

Research team

Aaron J. Kowalski, Ph.D.
Aaron J. Kowalski, Ph.D. Breakthrough T1D
Mark Anderson, M.D., Ph.D.
Mark Anderson, M.D., Ph.D. UCSF
Anil Bhushan, Ph.D.
UCSF
Edgar Engleman, Ph.D.
Stanford University
Seung Kim, M.D., Ph.D.
Seung Kim, M.D., Ph.D. Stanford University
Esther Latres, Ph.D.
Esther Latres, Ph.D.
Breakthrough T1D
Kyle Loh, Ph.D.
Kyle Loh, Ph.D.
Stanford University
Audrey Parent, Ph.D.
UCSF
Zoe Quandt, M.D.
UCSF
Judith Shizuru, M.D.
Judith Shizuru, Ph.D.
Stanford University
Brian Shy, Ph.D.
UCSF
Julie Sneddon, Ph.D.
Julie Sneddon, Ph.D.
UCSF
Qizhi Tang, Ph.D.
Qizhi Tang, Ph.D.
UCSF