Target Health Blog

New Viral Vector for Improved Gene Therapy in Sickle Cell Disease

October 21, 2019

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Gene Therapy
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Sickle cell disease affects about 100,000 people in the United States and millions worldwide. Sickle cell disease is an inherited blood disorder caused by a mutation, or misspelling, in the beta-globin gene (or ?-globin gene). This mutation causes hemoglobin, the main ingredient of blood cells, to produce sickle-shaped cells that can stick to the walls of blood vessels, causing blockage, pain, anemia, organ damage, and early death. With gene therapy, doctors modify the patient's bone marrow hematopoietic (blood-producing) stem cells in the lab by adding a normal copy of the beta-globin gene through the use of a viral vector. They then reinfuse the modified stem cells into the patient to produce normal, disc-shaped red blood cells.

According to an article published in Nature Communications (2 October 2019), a new and improved viral vector -- a virus-based vehicle that delivers therapeutic genes - has been developed for use in gene therapy for sickle cell disease. In advanced lab tests using animal models, the new vector was up to 10 times more efficient at incorporating corrective genes into bone marrow stem cells than the conventional vectors currently used, and it had a carrying capacity of up to six times higher. The development of the vector could make gene therapy for sickle cell disease much more effective and pave the way for wider use of it as a curative approach for the painful, life-threatening blood disorder.

For the past 30 years, researchers have been designing these beta-globin vectors in a reverse structural orientation, meaning the therapeutic genes incorporated into the virus are translated, or “read,“ from right to left by the viral vector-making machinery-much like reading an English sentence backwards. The reason for the reverse orientation is the sensitive expression of a key molecular component of the vector called intron 2. This segment is required for high-level beta-globin gene expression but gets clipped out during the normal vector preparation process if it is left in the natural, forward direction. Gene therapy trials using reverse-oriented vectors for sickle cell disease and beta-thalassemia have largely been encouraging, but this complicated gene translation process has made vector preparation and gene-transfer efficiency more difficult.  

About 10 years ago, the authors searched for an improved delivery vehicle -- like designing a better car -- and decided to undertake a radical redesign of the beta-globin vector. They came up with a unique work-around design that left intron 2 intact and created the new forward-oriented beta-globin vector. In contrast to the old vector, the gene sequence, or “message,“ of the new beta-globin vector is read from left to right -- like reading a normal sentence -- making the gene translation approach less complicated. The authors then tested the new vectors in mice and monkeys and compared the results to reverse-oriented vectors. Results showed that the new vectors could transfer a much higher viral load -- up to six times more therapeutic beta-globin genes than the conventional vectors -- and had four to 10 times higher transduction efficiency, a measure of the ability to incorporate corrective genes into repopulating bone marrow cells. The new vectors also showed a capacity for longevity, remaining in place four years after transplantation. The authors also found that they could be produced in much higher amounts than the conventional vectors, potentially saving time and lowering costs associated with large-scale vector production.

The new vector, for which the NIH holds the patent, still needs to undergo clinical testing in humans. Already an estimated 27 people with sickle cell disease have undergone experimental gene therapy using conventional vectors. Through its Cure Sickle Cell Initiative, NIH is working to accelerate the development of these and other new genetic therapies, including gene editing, with the goal of finding a cure for the disease. The initiative is part of NIH's larger multi-pronged approach to reducing the burden of blood disorders. People with sickle cell disease can find a clinical trial that is actively enrolling.

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