The path to a cure
More than sixty years ago, entertainer Danny Thomas envisioned a hospital that would treat children regardless of race, color, creed or their family's ability to pay. A facility where research would shine light into the darkness.
1958
St. Jude presents Lemuel Diggs, MD, with a $10,000 grant for his work on sickle cell disease. Over the course of his career, Diggs was critical in the research and dissemination of knowledge about sickle cell disease, and played an instrumental role in helping Danny Thomas as he envisioned St. Jude as a research hospital.
February 4, 1962
The hospital opens in Memphis, Tennessee
St. Jude opens during a turbulent era in American history. The star-shaped building designed by renowned African-American architect Paul Revere Williams immediately becomes the region's first fully integrated children's hospital.
Since it opened, families have never received a bill from St. Jude for treatment, travel, housing or food — so they can focus on helping their child live.
1968
African-American physician Rudolph Jackson, MD, joins the staff at St. Jude and helps establish the sickle cell program.
1977
St. Jude begins participating in the first major effort to understand the lifelong progression of sickle cell disease.
1983
A St. Jude cancer patient with both sickle cell disease and cancer undergoes a bone marrow transplant to target her cancer.
However, the procedure also cures her sickle cell disease, and she becomes the first person in the world cured of sickle cell disease through a bone marrow transplant. That kind of discovery occurs because St. Jude is committed to studying multiple pediatric diseases.
2003
BABYHUG, a landmark multi-center study led by St. Jude researcher Dr. Winfred Wang, begins enrolling patients with a goal of evaluating the safety and efficacy of a promising drug, hydroxyurea, in very young children with sickle cell disease. In 2011, the published results showed that hydroxyurea is safe in infants as young as 9 months old and offers significant benefits, including a substantial decrease in pain and hospitalizations.
2016
A Methodist Sickle Cell Disease Transition Clinic is created in collaboration with the Methodist Comprehensive Sickle Cell Center to help 18-year-olds make the leap from St. Jude to adult-care facilities of their choice. The transition clinic has continued to grow and now includes participation from the Diggs-Kraus Sickle Cell Center.
2018
St. Jude is the first healthcare organization to receive the Legacy Grant from The Links Foundation, Inc., to support the advancement of sickle cell disease research. Today, with early diagnosis and appropriate treatments, the life expectancy of children with sickle cell disease has increased.
2022
Uniting researchers from across the country
St. Jude recommits funding to Collaborative Research Consortium for Sickle Cell Disease. In an effort to develop novel cures and approaches for treating sickle cell disease, this research collaborative was organized by Dr. Mitch Weiss. Uniting researchers from across the country in an array of specialties, this work aims to push forward the progress toward effective, sustainable treatment or cure for the disease. The research consortium is examining genetic approaches to treat sickle cell disease and working to accelerate the therapeutic pipeline.
Today
Our legacy of researching cures for sickle cell disease continues.
- St. Jude leads the Sickle Cell Clinical Research and Intervention Program (SCCRIP), which studies how sickle cell disease progresses over time, from childhood into adulthood, and how we can improve the quality of life for sickle cell disease patients while we continue to search for cures.
- Although a bone marrow transplant is a potential “cure” for sickle cell disease, it is not an easy cure, and it has many complications. That is why St. Jude is enhancing our bone marrow transplantation program to further improve outcomes for children with sickle cell disease. The program has ongoing efforts and clinical trials aimed at reducing the transplant-associated side effects. Additionally, clinicians and investigators are working on using half matched donors (such as parents and siblings who are not a full match) to do transplants for individuals with sickle cell disease, making this treatment option available to many more patients.
- Most patients will not have a matched donor for bone marrow transplantation; therefore, St. Jude also continues to research alternate approaches to treat or cure sickle cell disease. Because sickle cell disease is caused by a single genetic mutation, it is an attractive target for gene editing. St. Jude has developed a gene editing program to develop safe and effective therapies for individuals with SCD and expects to begin enrolling patients on a new clinical trial evaluating a gene editing approach that was developed by St. Jude investigators. Working with collaborators, St Jude also participates in clinical trials of other gene therapies for SCD aimed at evaluating the safety and efficacy of these promising new treatments in pediatric populations.
- St. Jude faculty perform innovative laboratory research on sickle cell disease and other blood disorders. In these labs, St. Jude not only conducts basic research, but also uses translational research to bridge the gap from the lab to the bedside.
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