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René Maehr, PhD

Rene Maehr headshot- Associate Professor of Molecular Medicine, UMass Chan Medical School
- Co-Director, Pappas Stem Cell Differentiation Core (SCDC)
- Breakthrough T1D Barbara Dewey Cammett Center of Excellence in New England 

PhD in Pathology, Vrije Universiteit, Amsterdam, Netherlands
Postdoc, Harvard University, Cambridge, Massachusetts
Diplom, Albert Ludwig University of Freiburg, Germany

Type 1 Diabetes Research

Reprogramming Immune Tolerance for Regenerative Therapies

The Maehr lab is developing strategies at the intersection of stem cell biology, immunology, and functional genomics to engineer immune-compatible therapies for Type 1 Diabetes and beyond.  They are particularly focused on immune education and immunocloaking approaches to mitigate the need for systemic immunosuppression in allogeneic cell transplantation.

They engineer tolerance-inducing cells and organoids from pluripotent stem cells, enabling patient-specific and directed immune education. In parallel, they are advancing functional genomics-based strategies to discover effective strategies to educate immune cells and protect them from autoimmune attack post-transplantation.

New Funding & Research Advance Dr. Maehr’s Work Toward T1D Stem Cell Therapies

Dr. Maehr was awarded NIH and Breakthrough T1D funding to develop novel ways to protect stem cell-derived islets from autoimmune attack. Together with a recent publication providing new insights into gene regulation, the lab is working to advance strategies to engineer safer, more durable stem cell therapies toward our goal of a curative treatment for people living with type 1 diabetes.   

Dr. Maehr Named Co-Director of the Pappas Stem Cell Differentiation Core

The Diabetes Center of Excellence at UMass Chan Medical School named Drs. Sam Redick and René Maehr as co-directors of the Pappas Stem Cell Differentiation Core. Together, they will continue to advance stem cell–derived islet production and research, including gene editing to protect insulin-producing beta cells from autoimmune Type 1 diabetes. The ultimate goal is a cell-replacement therapy that won't require immunosuppressants.  

Publications

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