3-5: Biotechnology Flashcards
Recombinant DNA can be used for medical treatment. One example is treatment of patients with chemo-resistant leukemia. The patient’s __-cells can be reprogrammed to attack __-cells. (4 steps)
T-cells; B-cells.
- Remove most of the viral genome and replace it with a specially designed DNA construct that encodes a new protein that recognizes B-cells.
- Infect T-cells with the virus so they will express the new protein, a cell-surface receptor that recognizes B-cells.
- Transgenic T-cells are reprogrammed to attack and kill B-cells, killing the cancerous cells.
- Some of the transgenic T-cells survive and reproduce. These newly reproduced T-cells can identify and attack new cancerous B-cells.
Transgenic cells can be used to treat cancer. The transgenic cells are given new capabilities to ______ and ______ cancer cells. For a long-lasting “cure”, the transgenic cells must _________________ and _________.
recognize; attack
survive in the patient; proliferate
Response to transgenic-cell treatment is rapid and sustained. Upon infusion of transgenic T-cells, the patient experiences _______ _______ ______________ within the first month. If treatment is successful, patient shows no evidence of cancer for up to three years.
tumor lysis syndrome: chills, nausea, fever - signs showing that the treatment is working.
Limitations and risks of treatment (4)
- Cost: $20,000 per patient. T-cells must be synthesized specific to individual patient.
- Immune suppression: transgenic T-cells attack healthy B-cells.
- Tumor Lysis Syndrome - debris from dying tumor cells can damage kidneys and other organs.
- Cytokine storm: patient’s physiological response to the T-cell “attack” can be dangerous.
Hurdles to overcome in using transgenic cells (recombinant DNA) for medical treatment:
- How can you reprogram immune cells to attack each other?
- How can you insert new genes into a patient’s T-cells?
- Will those cells persist as a long-term “cure”?
- Design and insert new gene into the cells. This new gene can code for new cells that can attack immune cells.
- Use vectors as transport modules.
- Yes, evidence is strong from research so far.
An example of a vector is _________ ____. (3)
modified HIV.
- Vectors can be used to transfer genetic material into “target” cells.
- Normal HIV targets T-cells and inserts viral genome into the cell’s genome.
- Modified HIV inserted specifically engineered recombinant transgenes instead of viral genome.
Modified HIV treatment requires recombinant transgenes to be expressed in ______. The protein that recognizes the __-cells is a chimeric protein that’s encoded by fragments of several different genes (3).
T-cells.
B-cells.
1. VH fragment of DNA encodes the portion of the chimeric protein that recognizes B-cells; it is found on the extracellular surface of the transgenic T-cells.
2. Human CD&a Hinge and TM encodes the transmembrane domain of the chimeric protein.
3. 4-1BB encodes the intracellular domain of the chimeric protein, which activates T-cells that have “found” B-cells, causing them to kill B-cells.