Gene Therapy for Immunodeficiency

Gene therapy for immunodeficiency involves modifying a person’s wayward genes responsible for immune system problems. Scientists insert healthy copies of these genes into the patient's cells, often using a special virus as a delivery tool. Once corrected, these cells can produce properly functioning proteins that strengthen the immune system. This approach aims to address the root cause of immunodeficiency, potentially offering a long-term or permanent solution, reducing reliance on treatments like frequent infusions or antibiotics. Overall, gene therapy represents a promising advance in treating genetic immune disorders by restoring normal immune function at the DNA level.