The Benefits Of Gene Therapy

Improved Essays
Imagine living in a world where there was a cure for cancer and genetic diseases. Although it may sound impossible, it has already been done. With gene therapy, which is a technique where a gene that is either defective or missing is replaced with healthy ones through genetic engineering, doctors are able to treat people with cancer and immunodeficiencies.
Immunodeficiencies are, “Rare but life-threatening genetic diseases that severely compromise the integrity and function of the immune system” (Kumar et al. 1-2). Children born with these diseases have such a weak immune system that they usually die in the first few years after birth because their body cannot fight off what would usually pose no threat to a healthy child. One of these diseases
…show more content…
Recent clinical trials showed positive results for many different types of cancer. In one clinical trial, gene therapy was used to decrease the size of the cancer cells, so it could be removed three weeks later. Dr. Michael Blaese and Dr. French Anderson led a study that is proving the safety of gene therapy in cancer (Rosenberg 458-462). Another clinical trial has shown positive results for five out of nine metastatic patients treated by Morgan Et al. who responded positively to gene therapy treatment. A very recent clinical trial byt Rapoport et al. reported safety and efficiency of NY-ESO which is a “human derived, affinity enhanced TCR that recognizes a peptide shared by two CTAs” (Kumar et al. 8). In other words, the gene therapy was successful on the patients. Although you can not be treated for cancer with gene therapy the same way you can use radiation, chemotherapy, or surgery, it is a new technology that will one day be able to cure cancer as easily as …show more content…
One thing is the amount of people who have died due to clinical trials for gene therapy. There is one study three patients died during phase one of a gene therapy trial for brain cancer. Patient three died after being discharged from a treating center for phase one study 15 days after starting 30 mg dose of gene therapy (Brown and Lillicrap 1133-40). However, in every medical trial there are going to be loss of lives in order to cure the disease/cancer/immunodeficiency. In another study that used adenovirus as a delivery vehicle the levels of inflammatory cytokines increase, the high vector doses are elevated more than 50-fold and result in hepatotoxicity. Again, every clinical study will have situations where things go

Related Documents

  • Decent Essays

    There are 2 types of gene therapy they are “Germline therapy and Somatic therapy”. Germline therapy is a treatment that involves the adjustment of the genes inside the germ cells (ova or sperm). As zygote evolves, they would divide which, will then passed on the adjusted gene into different cells. While the Somatic therapy is the insertion of therapeutic…

    • 60 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Ricki Lewis’s The Forever Fix: Gene Therapy and the Boy Who Saved It tells the tale of gene therapy’s rocky road from a wild idea people considered to be a “daydream” to a growing field providing lucky individuals with treatment to prevent their life-shattering genetic diseases. In her novel, Lewis discusses two major biological concepts: mutation and gene expression. To give the reader the molecular basis for genetic disorders, mutation is briefly addressed.…

    • 1174 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Contrary to what one would expect based on the title of her book, The Forever Fix: Gene Therapy and the Boy Who Saved It, Ricki Lewis pens a narrative science focused on the milestones in the history of gene therapy, not just one success story (Lewis, 2012). Corey Haas, the boy who regained his vision after being sentenced to a life of blindness, is only one of the medical miracles mentioned; the book also devotes itself to presenting the theory and procedures behind gene therapy. As a supplement to the curriculum of the AP Biology course, the major biological concept of gene therapy in The Forever Fix: Gene Therapy and the Boy Who Saved It relates specifically to the third big idea in the AP Biology curriculum framework’s four major points.…

    • 1166 Words
    • 5 Pages
    Improved Essays
  • Superior Essays

    Patrick Hsu, a bioengineer at the Sulk Institute for Biological Studies, has begun studies using this biotechnology to model neurodegenerative disorders using monkeys. This is a huge advancement, for this would be a much more effective model than the previous mouse models being used. Another study has been done at Harvard in which the CRISPR/Cas9 system is being used to knock out the gene known to cause obesity. Researchers have also used this technology to reverse mutations that cause blindness and stop cancer cells from multiplying. The fact that this technology allows researchers to successfully do these things using model organisms opens up many possibilities for the use of using this technology to treat various diseases in…

    • 1490 Words
    • 6 Pages
    Superior Essays
  • Improved Essays

    The nucleic acids produced from the procedure of gene line therapy can be toxic to the chemical and biological properties. Forexample naked nucleic acids can interfere with coagulation or interference with cell function leading to death. The delivery system used for the gene transfer can also damage the systematic and cellular levels such as herpes virus from in vivo gene therapy. THE GENE DELIVERY PROCEDURES ARE ALSO TOXIS .(Gaccia p. 283, 284).…

    • 1028 Words
    • 5 Pages
    Improved Essays
  • Superior Essays

    Duchenne’s muscular dystrophy Duchenne’s Muscular Dystrophy Zachary Uecker Genetic Disease Abstract Duchenne’s muscular dystrophy is a genetic disease that targets skeletal muscles and over time, the muscles lose protein and are replaced by fats and connective tissue, making the skeletal muscles unusable. In this paper, the parts of Duchenne’s that will be covered are the method of transmission, statistics about Duchenne’s in the population, the pathophysiology, the body systems effected, signs and symptoms, age of onset, treatment/therapy options, psychological factors, prognosis, prevention techniques, ethical considerations, and how genetic counseling may be utilized for patients.…

    • 1182 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Yet another study lasting from 2001 to 2003 in Beijing noted that patients treated with p53 gene therapy saw the rate of tumor disappearance increase by 231% (Zhang et al. 2005). Legions of clinical trials in the East returned remarkable results for p53 gene therapy. Consequently, the Chinese FDA approved the treatment, under the trade name 'Gendicine', in 2004 (Jia, 2007). The Gendicine has been very effective in its use, but hasn't been the cut-and-dry 'cure' - it is merely another weapon in our arsenal of treatment…

    • 660 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Pro And Cons Of Eugenics

    • 1470 Words
    • 6 Pages

    With the results of different (human) genetic modification trials and the increase of gene editing technologies such as CRISPR, there have been contrasting public reactions to the information. In recent years, the topic of debate has been whether there should be limits or checks on the…

    • 1470 Words
    • 6 Pages
    Superior Essays
  • Improved Essays

    It can help save lives by changing the structure of a persons genes. It can make people smaller so we take up less food, energy, fuel, fabric, shoes, furniture, etc. Also, it can give us cat-like eyes so we can see better in the dark and we won't have to use as many lights. Gene therapy can prevent blindness, some cancers, and sometimes it can cure HIV/AIDS. As a success story, in 1982, a company named Genetech, genetically engineered E. Coli.…

    • 1041 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    While the technique is still in its infancy it is already beginning to show a lot of promise. When this method was tested to treat rats infected with the HIV virus, just a single injection of CRISPR in to the rats tails was able to remove over 50% of the virus from the rats cells. It is possible that in a few decades that HIV and other viruses could be eliminated. There is also the possibility of curing cancer this way. By genetically engineering peoples cells, we can make their immune systems better and detecting and eliminating the cancer…

    • 865 Words
    • 4 Pages
    Improved Essays
  • Decent Essays

    The whole concept of gene modification is frightening, since genes are what make us and if that goes wrong everything could go wrong. Just like in live-action movies, if there is an advanced concept and that ends up in the wrong hands, the end result could be corrupt or disastrous. For example, in the movie “The Amazing Spiderman” a scientist turns himself into a human lizard, where he takes a reptile’s DNA and creates a drug to regrow his missing arm. Human gene therapy, seen from an evolutionary point of view, could be very surprising and unexpected since it is not the environment, such as selective pressure, that is contributing to evolution but is the organism itself. Depending on the perspective, gene therapy does not adhere to the rules of natural selection.…

    • 375 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    Stem Cell Modification

    • 459 Words
    • 2 Pages

    Question: Can Stem Cell Modification cause unrealized consequences? Claim: Stem Cell modification can cause unrealized consequences Evidence 1: “While the positive therapeutic outcome was celebrated as a breakthrough in gene therapy, a serious drawback subsequently became evident. By February 2005, three children out of seventeen who had been successfully treated for X-linked SCID developed leukemia because the vector inserted near an oncogene (a cancer-causing gene), inadvertently causing it to be inappropriately expressed in the genetically-engineered lymphocyte target cell.…

    • 459 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Recessive Genetic Traits

    • 676 Words
    • 3 Pages

    I think that gene therapy is both good and bad. It's good because this allows a doctor to treat a disorder without giving the patient drugs or surgery. This is also bad because one of the risks are possibly tumors, and…

    • 676 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Innovative technology and cancer research surround today’s world; experts are learning new things daily. At first glance, chemotherapy or radiation therapy seem to be the only options of treatment; however, this…

    • 1504 Words
    • 7 Pages
    Superior Essays
  • Improved Essays

    Gene therapy has been researched and studied for decades, however it has only ever reached a partial amount of success. It’s very difficult to introduce new genes to the body, just like it’s incredibly complicated to keep them within the body over a required period of time. The main points that will be addressed about the limitations of gene therapy will be, gene delivery, and activation, immune response, disrupting important genes in target cells, and commercial viability. In the aspect of gene delivery and activation, it is crucial for the altered genes to reach its proper destination, since bringing a gene to the wrong cells could cause various medical issues and health problems to the patient. This brings us to more questions, as once the gene reaches its destination, it must be activated, and remain at that state for a certain period of time.…

    • 1110 Words
    • 4 Pages
    Improved Essays

Related Topics