Gene therapy cures sickle cell anemia patient
Attaining a new breakthrough in the field of medical science, French doctors have successfully cured a sickle cell anemia patient using an experimental gene therapy.
Doctors at Necker Children’s Hospital in Paris reported that a teenager suffering from sickle cell disease achieved full remission in wake of the experimental gene therapy. The patient started the therapy at the age of 13 years.
Individuals with sickle cell disease have abnormal hemoglobin in their red blood cells, which leads the blood to clog in the minute vessels and organs of the body.
After a period of fifteen months since treatment, the patient no longer needed medication as his blood cells showed no signs of the sickle-cell disease.
Dr. Philippe Leboulch, a professor of medicine at the University of Paris, said, “Since therapy was applied, he hasn’t had any pain, any complications. He is free of any transfusions. He plays sports and goes to school. So we are quite pleased with the results.”
The successful use of the experimental gene therapy for curing sickle cell anemia patients was detailed in the most recent edition of the New England Journal of Medicine.
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