The FDA reports on a monoclonal drug called basiliximab, or more commonly known as, Simulect®. Drugs in this class work by using monoclonal antibodies. Monoclonal antibodies are produced when an antigen in injected into an animal, the animal’s immune system responds by producing antibodies, and the B cells are isolated and fused with malignant plasma cells. The fusion of these two cells is called a hybridoma. The B cell provides the genes that code for specific antibody production while the malignant plasma cells offer the ability to divide continuously. The byproducts of this process can be harnessed and used in a variety of monoclonal medications.
Simulect®, or basiliximab, is a monoclonal drug that is administered via injection. This drug serves as an immunosuppressant and is given to kidney transplant patients. By suppressing the patient’s immune system, the likelihood of organ rejection is much lower. This drug is given in two doses, one within two hours of surgery, and one 4 days after. This medication works by preventing binding with IL-2 receptors on the surface of activated T cells and therefore limiting the effectiveness of the immune response.
This medication has the following possible side effects; nausea, stomach pain, diarrhea, constipation, or redness/pain at the site of injection. Individuals with a hypersensitivity may experience anaphylaxis characterized by; tachycardia, hypotension, dyspnea, wheezing, and respiratory failure, in which case the treatment should be suspended immediately. Because this drug compromises the adaptive immune system, individuals will be more susceptible to other infections and should take the necessary precautions. Also, the FDA warns that it is still unknown whether or not this medication will have a long lasting effect on the immune system and the ability to respond to antibodies.