AAV (adeno-associated virus) vector technology

AAV (adeno-associated virus) vector technology uses modified viruses to deliver genetic material into cells. These viruses are engineered to be safe, losing their ability to cause illness, and are used to carry specific genes into the body to treat genetic diseases or modify cell functions. Once inside the cells, the delivered gene can produce a desired protein, potentially correcting or compensating for a genetic defect. AAV vectors are popular because they efficiently target various tissues, have low immune response, and can provide long-lasting effects, making them a valuable tool in gene therapy.