Dialing Up Fetal Hemoglobin Dials Down Sickle Cell Disease
Deactivating a single protein corrects sickle cell disease in mice; study opens door to new generation of therapies for this and other blood disorders
BOSTON, Oct. 13, 2011 /PRNewswire-USNewswire/ — Flipping a single molecular switch can reverse illness in a model of sickle cell disease, according to a study by researchers at Children’s Hospital Boston and Dana-Farber Cancer Institute. When turned off, the switch, a protein called BCL11A, allows the body to manufacture red blood cells with an alternate form of hemoglobin unaffected by the mutation that causes the disease.
The findings – reported online by a research team led by Stuart Orkin, MD, of the Dana-Farber/Children’s Hospital Cancer Center (DF/CHCC) in the journal Science on October 13 – provide strong evidence that BCL11A could be a powerful treatment target for a significant global health problem, one that affects between 75,000 and 100,000 people in the United States alone.
“This study provides the first proof of principle that BCL11A might serve as a target for treating sickle cell disease, and related blood disorders such as the thalassemias,” said Orkin, associate chief of the division of hematology/oncology at Children’s Hospital Boston and chair of pediatric oncology at Dana-Farber.
First described over 100 years ago, sickle cell disease (or sickle cell anemia) is an inherited blood disease caused by a single mutation in one of the components of hemoglobin, the oxygen-carrying protein in red blood cells. The mutation reduces the protein’s ability to carry oxygen, and forces the cells to curve into a distinctive crescent or sickle shape, causing them to painfully accumulate and break apart in small blood vessels.
The disease can only be cured with a bone marrow or stem cell transplant, though difficulties in finding well-matched donors and the complications associated with transplantation rules this out as an option for most patients. A drug called hydroxurea can provide some relief, but its mechanism of action is unclear and its efficacy unpredictable from patient to patient.
Our bodies can actually manufacture two forms of hemoglobin: the adult form susceptible to the sickle cell mutation, and a fetal form that is largely produced during development and for a short time after birth. Affected children first experience sickle cell symptoms around the time that our bodies switch from producing red blood cells with fetal hemoglobin to those with adult hemoglobin (approximately 3-6 months of age).
BCL11A first drew serious attention in genome-wide association studies of sickle cell disease patients. Shortly after the genomic data came to light, Orkin, who is also a Howard Hughes Medical Institute investigator and the David G. Nathan Professor of Pediatrics at Harvard Medical School, and his colleagues showed that by genetically knocking out BCL11A they could activate fetal hemoglobin and silence mutated adult hemoglobin in cultured normal human red cell progenitors.
“The red blood cell lineage performs a balancing act when it comes to manufacturing hemoglobin,” Orkin explained. “Increasing the production of one form reduces production of the other.”
In the current study, Orkin’s team set out to assess the impact of removing BCL11A from the red blood cell lineage in the adult. Using two different mouse models of human sickle cell disease as a means of cross-validation, they engineered a system whereby they could selectively turn the protein off just in the immature progenitor cells that give rise to red blood cells.
The results in these mice were striking. Relieved of BCL11A’s influence, the mice in both models started producing red blood cells that showed no evidence of sickling, with no adverse impact on the level of cell production. Eighty-five percent of the red blood cells in the mice carried fetal hemoglobin, and on average, 30 percent of the hemoglobin contained within these cells was of the fetal type. The mice also showed great improvement in a number of physiologic and clinical features.
“We knew from previous clinical studies that the body needs to produce cells containing only 15 to 20 percent fetal hemoglobin to reverse disease,” Orkin said, “With these results we know now we have a target that, if we can develop ways to inactivate or silence it clinically, could be very beneficial to people with sickle cell.”
He and his colleague are already pursuing several lines of investigation aimed at broadening their understanding of BCL11A and translating their mouse findings into potential treatments. “We want to better understand the network of genes and proteins that interact with BCL11A, to see if any of them might also stand out as targets,” he said. “We also are screening the protein against libraries of chemicals in the hope of identifying compounds that interfere with it, and think it may also hold promise as a target for genetic therapies.”
The study was supported by the National Heart, Lung, and Blood Institute; the National Cancer Institute; the National Institute of Diabetes and Digestive and Kidney Diseases, the Howard Hughes Medical Institute, and the Marie Betzner Morrow Endowment.
Children’s Hospital Boston
Children’s Hospital Boston is home to the world’s largest research enterprise based at a pediatric medical center, where its discoveries have benefited both children and adults since 1869. More than 1,100 scientists, including nine members of the National Academy of Sciences, 11 members of the Institute of Medicine and nine members of the Howard Hughes Medical Institute comprise Children’s research community. Founded as a 20-bed hospital for children, Children’s Hospital Boston today is a 396 bed comprehensive center for pediatric and adolescent health care grounded in the values of excellence in patient care and sensitivity to the complex needs and diversity of children and families. Children’s also is the primary pediatric teaching affiliate of Harvard Medical School. For more information about research and clinical innovation at Children’s, visit: http://vectorblog.org.
SOURCE Children’s Hospital Boston