In a groundbreaking study, scientists have discovered a way to reprogram gene therapy vectors, paving the way for more efficient treatments of genetic diseases. The team, led by researchers at the University of Toronto, found a way to modify the capsids of viral vectors, allowing them to be tailored to an individual’s genetic makeup. This could potentially reduce the amount of time and money it takes to deliver gene therapy treatments. It could also improve the effectiveness of the treatments. The study is a major step forward in the development of gene therapy, and holds great promise for the future of treating genetic diseases.

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source: Phys.org