Mia Robinson, shown above, is one of many Americans living with sickle cell disease (SCD).
Content sponsored by Vertex Pharmaceuticals Incorporated
Chances are you probably know someone who is or has been impacted by sickle cell disease (SCD). In fact, 1 in 13 African Americans have the sickle cell trait. While it’s considered a rare genetic disease, it’s actually the most common inherited blood disorder in the world. Every September, we recognize Sickle Cell Awareness Month in the U.S. As we mark the month this year, we’re taking this opportunity to raise awareness about this devastating disease, elevate voices in the community to share their experience living with the disease and highlight potential treatments that scientists at Vertex Pharmaceuticals have been working on. Read on (and check out the video below!) to learn more about the underlying cause of SCD and how scientists are currently investigating a potential gene-editing therapy to address this serious disease.
This video talks about sickle cell disease (SCD), which is caused by inherited changes in the beta-globin (HBB) gene. The mutation leads to issues with the production of hemoglobin, the protein crucial for allowing red blood cells to carry oxygen throughout the body. Living with SCD currently requires a lifetime of treatment and can result in painful symptoms and reduced life expectancy. Vertex scientists are investigating the use of CRISPR/Cas9 gene-editing technology to hopefully turn on the body’s natural machinery to increase the production of hemoglobin that can carry oxygen properly.
People inherit SCD because of a “misspelling” in their DNA. This causes red blood cells to be a different shape and become stiffer and stickier, making it difficult for them to travel throughout the body. This leads to many different problems, and people living with SCD often experience symptoms and complications including pain crises, strokes, anemia, jaundice, and symptoms of heart failure. The sickle cell trait can actually be a good thing – it evolved over time to protect people against severe malaria. Because of the way it has stayed with populations through the slave trade in the U.S. and economic migration to the Americas, people of certain nationalities have a higher likelihood of having the sickle cell trait than others, including:
Today, the only cure for SCD is a stem cell transplant from a matched donor and it is only available to a small fraction of people living with SCD.
The cause of SCD has been known for decades — in fact, SCD is considered the first molecular disease — but many patients are still waiting for a treatment that addresses the underlying cause of their disease. Vertex’s investigational approach uses CRISPR/Cas9 gene-editing technology to turn on the body’s natural machinery to increase the production of hemoglobin that can carry oxygen properly. They’re bringing together best-in-class research teams, technologies, and manufacturing capabilities in the hopes of bringing potentially transformative therapies to patients, like people with SCD, as quickly as possible.
To learn more about Vertex’s work in sickle cell disease and other serious diseases, visit www.vrtx.com/en-us
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