National Institutes of Health-funded scientists have corrected sickle cell disease in adult laboratory mice by activating production of a special blood component normally produced before, but not after, birth.
“This discovery provides an important new target for future therapies in people with sickle cell disease,” said Susan B Shurin, MD, acting director of the NIH's National Heart, Lung, and Blood Institute (NHLBI), which co-funded the study. “More work is needed before it will be possible to test such therapies in people, but this study demonstrates that the approach works in principle.”
Researchers at Harvard Medical School in Boston and the University of Texas at Austin corrected sickle cell disease in mice that had been bred to have the inherited blood disorder. The NHLBI, the National Cancer Institute, and the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) — all part of the NIH – funded the research. The results of the study will appear online Oct. 13 in the journal Science.
Sickle cell disease results from an abnormality in haemoglobin, the protein found in red blood cells that is responsible for transporting oxygen throughout the body. People living with sickle cell disease have two copies of an altered gene that produces sickle haemoglobin instead of normal adult haemoglobin. Sickle haemoglobin changes shape after releasing its oxygen, causing the red blood cell to become stiff, misshapen and sticky, and slowing blood flow to tissues. This process damages organs and causes pain.
The study tested a new approach to increasing the production of a third form of haemoglobin—fetal haemoglobin. Production of fetal haemoglobin predominates before birth, but turns off thereafter as adult haemoglobin production takes over. People with sickle cell disease are unable to make normal adult haemoglobin, and instead make sickle haemoglobin starting in infancy.
An elevated level of fetal haemoglobin within the red blood cell reduces the tendency of sickle haemoglobin to change the shape of red blood cells. Considerable NIH- supported research has shown that the drug hydroxyurea increases production of fetal haemoglobin and reduces the number of pain crises and other complications of sickle cell disease in adults and children. However, not all patients respond well to hydroxyurea, and adverse side effects are a concern.
The current study explores a more targeted approach to increasing fetal haemoglobin production. It builds upon earlier studies by Stuart Orkin, M.D., and his team at Harvard Medical School, Children’s Hospital of Boston, and the Howard Hughes Medical Institute, Boston, which discovered that a protein called BCL11A normally suppresses the production of fetal haemoglobin soon after birth. The researchers viewed the BCL11A protein as a target for therapy and decided to see what would happen if they blocked production of the protein.
“This important advance in the battle against sickle cell disease is another outstanding example of how great things can happen when work proceeds from bench to bedside, and back to the bench,” said Griffin P Rodgers, MD, MACP, director of NIDDK. “We hope that one day, this discovery and any that build upon it will translate into a viable treatment option for those suffering from this devastating illness.”
The current paper details how the research team silenced the mouse gene that produces the BCL11A protein in mice with sickle cell disease. Silencing the gene turned off production of the BCL11A protein and allowed the adult mice to continue to produce fetal haemoglobin. It appears to have eliminated disease symptoms without affecting other aspects of blood production.
Approximately 100,000 Americans live with sickle cell disease. It is most prevalent in people of African, Hispanic, Mediterranean, and Middle Eastern descent. There is no widely available cure for sickle cell disease. Bone marrow transplants have cured some patients, but the treatment is not without risk and most patients do not have relatives who can donate compatible and healthy bone marrow to them.
Part of the National Institutes of Health, the National Heart, Lung, and Blood Institute (NHLBI) plans, conducts, and supports research related to the causes, prevention, diagnosis, and treatment of heart, blood vessel, lung, and blood diseases; and sleep disorders. The Institute also administers national health education campaigns on women and heart disease, healthy weight for children, and other topics.
NIH, the nation's medical research agency, a component of the US Department of Health and Human Services. It is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases.