Blood and Marrow Transplant
Stem cells hold the promise of treatments and cures for more than 70 major diseases.
Dating back to the world’s first successful bone marrow transplant in 1968, the University of Minnesota Medical School has been, and continues to be, a leader in stem cell research and regenerative medicine—a field of innovative therapies that enable the body to heal itself.
Now with new discoveries being made, we’re working on cures for everything from diabetes to dementia.
The Medical School’s blood and marrow transplant research has a legacy of changing perspectives around what is medically possible for children battling some of the world’s most complex, life-threatening diseases. Beyond the first successful bone marrow transplant (BMT) in the world, the Medical School has a history of firsts, including:
- The first transplant to treat a patient with lymphoma (1975)
- The first transplant to treat an inherited metabolic disease (1982)
- The first double umbilical cord blood transplant (1999)
- The first umbilical cord blood transplant performed using pre-implantation genetic testing to ensure a perfect tissue match (2000)
BMT Research Across the U
Pediatric Blood & Marrow Transplantation Center
Our clinical center for care, noted for exceptional and innovative blood and marrow transplantation, research, and education. John Wagner, Jr., MD, directs this center.
Division of Hematology, Oncology & Transplantation
Committed to providing the highest quality care based on cutting edge research to patients with cancer or non-malignant hematologic diseases such as sickle cell disease. Dedicated to advancing research on the biological underpinnings of cancer, stem cell biology, sickle cell anemia, endothelial cell biology, and tumor immunology. Over 50 full-time academic investigators involved in interdisciplinary research and patient care are devoted to training the next generation of academic leaders.
Division of Blood & Marrow Transplantation
Our clinical program is recognized as the second largest unrelated donor transplant programs in the country, and one of the largest umbilical cord blood transplant centers worldwide.
Stem Cell Institute
As the first such institute in the nation, our Stem Cell Institute is a national leader in the field of stem cell research. Researchers and faculty explore the science of stem cell biology, respond to the medical needs of today, and educate the researchers of tomorrow.
Molecular & Cellular Therapeutics
Molecular and Cellular Therapeutics enables the translation of novel, experimental research into medicine for use in human clinical trials. Their technical, development, regulatory, and quality expertise ensure that all FDA requirements are satisfied and products are delivered to the patient in the shortest possible time.
Transplant Biology & Therapy Program at the Masonic Cancer Center
Made up of 41 members representing five departments and three schools within the University of Minnesota's Academic Health Center. Members of this program seek to reduce or eliminate factors limiting hematopoietic stem cell transplantation, such as regimen-related toxicities, graft-versus-host disease (GVHD), and delayed reconstitution of immunity.
Eradicating Epidermolysis Bullosa
Epidermolysis bullosa (EB) is an often life-threatening skin disease found primarily in children. Children with EB face infections and debilitating pain. Skin often must be bandaged to reduce damage and prevent infection. Medical School faculty began the first and only program in the world that offers blood and marrow transplant as a treatment for the most severe types of EB.
While past treatment focused on topical therapy, similar to what is done for burn patients, our doctors were the first to explore BMT as an option for patients with severe EB. The first child to receive BMT for EB took place at University of Minnesota Masonic Children’s hospital in 2007. Since then, we have provided transplant as a therapy option to about five patients each year. And we are exploring genomic mapping techniques that might allow us to fix a child’s DNA before birth.