Safer transplants, better outcomes

Researchers in Regensburg, Erlangen and Würzburg work together in the CRC Transregio 221, that focuses on unsolved challenges in the treatment of patients with leukemia or lymphoma.

CRC TRR 221's mission

Within the Collaborative Research Centre/Transregio (CRC/TRR) 221 innovative immune modulation strategies are investigated to separate graft-versus-host disease (GvHD) from GvL (graft-versus-leukemia) effects in order to enhance the safety and efficacy of allogeneic hematopoietic stem cell transplantation (HSCT) in the future.

RESEARCH

We investigate basic immunological mechanisms to understand and ultimately strengthen graft-versus-leukemia (GvL) effects of donor immune cells after allogeneic hematopoietic stem cell transplantation in order to avoid leukemia relapse. We also study graft-versus-host immune reactivity to non-hematopoietic patient tissues (f.e. gut, skin), which we intend to prevent or at least mitigate by innovative immunomodulatory strategies.

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FEATURED SCIENTIST

Dennis Harrer is principal investigator of project A07, which investigates long-lived, self-renewing, minimally differentiated T memory stem cells (TSCM) as a platform technology for chimeric antigen receptor (CAR) T cell therapy.  TSCM are thought to overcome barriers to effective and safe salvage therapy with donor-derived CAR T cells after allogeneic hematopoietic stem cell transplantation.

FEATURED PROJECTS

Principal investigators Petra Hoffmann, Michael Rehli, and Matthias Edinger of project B07 work on GvHD therapy with donor regulatory T cells (Treg) aiming to enhance the efficacy of this cell population for the prophylaxis and/or treatment of acute and chronic GvHD after allogeneic HSCT.

The CRC TRR 221 researchers are seriously committed to bridge the gap between basic and translational immunology in the field of allogeneic hematopoietic stem cell transplantation and cellular therapy. They strive to achieve our fundamental mission: to improve the safety and efficacy of these important treatment modalities for patients with high-risk hematologic malignancies and severe stem cell disorders.

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