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MEDTECH Given the potential of CRISPR gene-editing techniques and CAR T-cell therapy demonstrated in this trial, what implications might these advancements have for the broader field of hematological disease management?
In a groundbreaking medical trial, a new CRISPR gene-editing technique has been used to successfully treat a patient with a form of leukemia that was resistant to all conventional treatments. This innovative approach, which involved the use of CAR T-cell therapy and base editing, could potentially revolutionize the treatment of various diseases that affect the development of the blood, bone marrow, and immune systems.
Key Points:
- Alyssa Tapley, a 13-year-old girl, was diagnosed with T-cell leukemia, a form of the disease that is more challenging to treat and was resistant to all conventional treatments, including chemotherapy and bone marrow transplant.
- Dr. Waseem Qasim and his team at Great Ormond Street Hospital for Children in London conducted a trial using a new CRISPR gene-editing technique. This involved the use of CAR T-cell therapy and base editing, a gentler form of gene editing that changes single letters of the DNA code without causing a cut.
- Alyssa underwent the trial and received an infusion of CAR T cells. Five weeks later, doctors tested her bone marrow and found no trace of leukemia. Alyssa has been in remission for one year and is currently leukemia-free.
Additional Points:
- The trial faced several challenges, including the collection of cells from a patient who had already undergone extensive chemotherapy, and the issue of training T cells to fight other T cells without them fighting each other.
- The new treatment approach has the potential to be used for a larger number of patients. The team’s ambition is to take cells from a healthy donor and create a bank of cells that can be given to multiple recipients.
- The trial represents the first application of base editing in a human therapy. Base editing was only reported in 2016, and this trial marks a significant milestone in its application.
Conclusion:
- This trial represents a significant breakthrough in the use of CRISPR gene-editing techniques for the treatment of diseases that are resistant to conventional treatments. The success of this trial could pave the way for the development of new treatments for a range of conditions that affect the blood, bone marrow, and immune systems.
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