Gene Therapy Write for us
Human gene therapy aims to modify or manipulate the expression of a gene or alter the biological properties of living cells for therapeutic use
Gene therapy is a technique that changes a person’s genes to treat or cure a disease. Gene therapies can work through several mechanisms:
Replacement of a pathogenic gene with a healthy copy of the gene.
Inactivation of a pathogenic gene that does not work properly.
Introducing a new or modified gene into the body to help treat disease.
Gene therapy products are being studied to treat diseases such as cancer, genetic diseases, and infectious diseases.
There are different types of gene therapy products, including:
Plasmid DNA: Circular DNA molecules can be genetically engineered to carry therapeutic genes into human cells.
Viral Vectors: Viruses have the natural ability to introduce genetic material into cells and therefore some gene therapy products are derived from viruses. Once viruses have been modified to eliminate their ability to cause infectious diseases, these modified viruses can be used as vectors (vehicles) to transport therapeutic genes into human cells.
Bacterial vectors: Bacteria can be modified to prevent them from causing infectious diseases and then used as vectors (vehicles) to transport therapeutic genes to human tissues.
Human gene editing technology: The goals of gene editing are to alter harmful genes or repair mutated genes.
Patient-derived cell gene therapy products – Cells are removed from the patient, genetically modified (often using a viral vector), and then returned to the patient.
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