iNDICA NEWS BUREAU-
Scientists have reported an innovative gene-based treatment that modifies a patient’s own blood-forming stem cells to correct the mutation responsible for sickle cell disease.
The clinical trial, aimed at discovering a cure for sickle cell disease, a painful genetic blood disorder with limited treatment options, was conducted as part of the multi-center ‘RUBY Trial.’
Eighteen patients, including two treated at Cleveland Clinic Children’s in the US, underwent a procedure where their stem cells were first collected for gene editing. They then received chemotherapy to clear the remaining bone marrow, making room for the repaired cells, which were later infused into their bodies.
The treatment was well-tolerated with no serious side effects reported. Following treatment, all patients successfully regained their white blood cells and platelets.
Researchers noted that all patients have remained free of painful events since treatment, and those followed for five months or longer have seen their anemia resolve.
“It’s encouraging that this gene-editing treatment continues to show promising efficacy for sickle cell patients,” said Rabi Hanna from Cleveland Clinic Children’s and the RUBY trial’s presenting investigator.
Sickle cell disease is a genetic disorder that causes red blood cells to be misshapen similar to a sickle. In this condition, the abnormal cells block blood flow and break apart easily, leading to problems such as severe pain, liver and heart issues, and a shorter life span, typically in the mid-40s.
