Month: March 2026

Gene therapy aims to treat disease by adding, editing, or regulating genetic material within a patient’s cells. The effectiveness of these therapies depends less on the genetic instructions themselves and more on how precisely, safely, and efficiently those instructions reach the right cells. Early gene therapies struggled with immune reactions, limited targeting, and short-lived effects. New delivery methods are changing that landscape by improving accuracy, durability, and safety while expanding the range of treatable diseases.Cutting-edge viral vector platformsViral vectors remain a central delivery tool because viruses naturally enter cells. Recent advances focus on making them more selective and less likely…