Gene therapy involves altering the genes inside your body’s cells in an effort to treat or stop disease.
Genes contain your DNA — the code that controls much of your body’s form and function, from making you grow taller to regulating your body systems. Genes that don’t work properly can cause disease.
Gene therapy replaces a faulty gene or adds a new gene in an attempt to cure disease or improve your body’s ability to fight disease. Gene therapy holds promise for treating a wide range of diseases, such as cancer, cystic fibrosis, heart disease, diabetes, hemophilia and AIDS.
Researchers are still studying how and when to use gene therapy. Currently, in the United States, gene therapy is available only as part of a clinical trial. In this article, Pritish Kumar describes the knowledgeable facts about Gene therapy.
Why it’s done
Gene therapy is used to correct defective genes in order to cure a disease or help your body better fight disease.
Researchers are investigating several ways to do this, including:
Replacing mutated genes. Some cells become diseased because certain genes work incorrectly or no longer work at all. Replacing the defective genes may help treat certain diseases. For instance, a gene called p53 normally prevents tumor growth. Several types of cancer have been linked to problems with the p53 gene. If doctors could replace the defective p53 gene, that might trigger the cancer cells to die.
Fixing mutated genes. Mutated genes that cause disease could be turned off so that they no longer promote disease, or healthy genes that help prevent disease could be turned on so that they could inhibit the disease.
Making diseased cells more evident to the immune system. In some cases, your immune system doesn’t attack diseased cells because it doesn’t recognize them as intruders. Doctors could use gene therapy to train your immune system to recognize the cells that are a threat.
Gene therapy has some potential risks. A gene can’t easily be inserted directly into your cells. Rather, it usually has to be delivered using a carrier, called a vector.
The most common gene therapy vectors are viruses because they can recognize certain cells and carry genetic material into the cells’ genes. Researchers remove the original disease-causing genes from the viruses, replacing them with the genes needed to stop disease.
This technique presents the following risks:
Unwanted immune system reaction. Your body’s immune system may see the newly introduced viruses as intruders and attack them. This may cause inflammation and, in severe cases, organ failure.
Targeting the wrong cells. Because viruses can affect more than one type of cells, it’s possible that the altered viruses may infect additional cells — not just the targeted cells containing mutated genes. If this happens, healthy cells may be damaged, causing other illness or diseases, such as cancer.
Infection caused by the virus. It’s possible that once introduced into the body, the viruses may recover their original ability to cause disease.
Possibility of causing a tumor. If the new genes get inserted in the wrong spot in your DNA, there is a chance that the insertion might lead to tumor formation.
The gene therapy clinical trials underway in the U.S. are closely monitored by the Food and Drug Administration and the National Institutes of Health to ensure that patient safety issues are a top priority during research.
What you can expect
Currently, the only way for you to receive gene therapy is to participate in a clinical trial. Clinical trials are research studies that help doctors determine whether a gene therapy approach is safe for people. They also help doctors understand the effects of gene therapy on the body.
Your specific procedure will depend on the disease you have and the type of gene therapy being used.
For example, in one type of gene therapy:
- You may have blood drawn or you may need bone marrow removed from your hipbone with a large needle.
- Then, in a lab, cells from the blood or bone marrow are exposed to a virus or another type of vector that contains the desired genetic material.
- Once the vector has entered the cells in the lab, those cells are injected back into your body into a vein or into tissue, where your cells take up the vector along with the altered genes.
Viruses aren’t the only vectors that can be used to carry altered genes into your body’s cells. Other vectors being studied in clinical trials include:
Stem cells. Stem cells are the cells from which all other cells in your body are created. For gene therapy, stem cells can be trained in a lab to become cells that can help fight disease.
Liposomes. These fatty particles have the ability to carry the new, therapeutic genes to the target cells and pass the genes into your cells’ DNA.
Types of Gene Therapy
Basically, there are two types of gene therapy
Somatic Gene Therapy
This type usually occurs in the somatic cells of human body. This is related to a single person and the only person who has the damaged cells will be replaced with healthy cells. In this method, therapeutic genes are transferred into the somatic cells or the stem cells of the human body. This technique is considered as the best and safest method of gene therapy.
Germline Gene Therapy
It occurs in the germline cells of the human body. Generally, this method is adopted to treat the genetic, disease causing-variations of genes which are passed from the parents to their children. The process involves introducing a healthy DNA into the cells responsible for producing reproductive cells, eggs or sperms. Germline gene therapy is not legal in many places as the risks outweigh the rewards.
Application of Gene Therapy
- It is used in the replacement of genes that cause medical ill-health
- The method generally destroys the problem causing genes
- It helps the body to fight against diseases by adding genes to the human body
- This method is employed to treat diseases such as cancer, ADA deficiency, cystic fibrosis, etc.
The possibilities of gene therapy hold much promise. Clinical trials of gene therapy in people have shown some success in treating certain diseases, such as:
- Severe combined immune deficiency
- Blindness caused by retinitis pigmentosa
But several significant barriers stand in the way of gene therapy becoming a reliable form of treatment, including:
- Finding a reliable way to get genetic material into cells
- Targeting the correct cells
- Reducing the risk of side effects
Gene therapy continues to be a very important and active area of research aimed at developing new, effective treatments for a variety of diseases.