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7.6 Diseases Associated with Depressed or Overactive Immune Responses (47/71) -- Fundamentals of Anatomy and Physiology

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7.6 Diseases Associated with Depressed or Overactive Immune Responses

7.6 Diseases Associated with Depressed or Overactive Immune Responses Learning Objectives By the end of this section, you will be able to: - Discuss inherited and acquired immunodeficiencies - Explain the four types of hypersensitivity and how they differ - Give an example of how autoimmune disease breaks tolerance This section is about how the immune system goes wrong. When it goes haywire, and becomes too weak or too strong, it leads to a state of disease. The factors that maintain immunological homeostasis are complex and incompletely understood. Immunodeficiencies As you have seen, the immune system is quite complex. It has many pathways using many cell types and signals. Because it is so complex, there are many ways for it to go wrong. Inherited immunodeficiencies arise from gene mutations that affect specific components of the immune response. There are also acquired immunodeficiencies with potentially devastating effects on the immune system, such as HIV. Inherited Immunodeficiencies A list of all inherited immunodeficiencies is well beyond the scope of this chapter. The list is almost as long as the list of cells, proteins, and signalling molecules of the immune system itself. Some deficiencies, such as those for complement, cause only a higher susceptibility to some Gram-negative bacteria. Others are more severe in their consequences. Certainly, the most serious of the inherited immunodeficiencies is severe combined immunodeficiency disease (SCID). This disease is complex because it is caused by many different genetic defects. What groups them together is the fact that both the B cell and T cell arms of the adaptive immune response are affected. Children with this disease usually die of opportunistic infections within their first year of life unless they receive a bone marrow transplant. Such a procedure had not yet been perfected for David Vetter, the “boy in the bubble,” who was treated for SCID by having to live almost his entire life in a sterile plastic cocoon for the 12 years before his death from infection in 1984. One of the features that make bone marrow transplants work as well as they do is the proliferative capability of haematopoietic stem cells of the bone marrow. Only a small amount of bone marrow from a healthy donor is given intravenously to the recipient. It finds its own way to the bone where it populates it, eventually reconstituting the patient’s immune system, which is usually destroyed beforehand by treatment with radiation or chemotherapeutic drugs. New treatments for SCID using gene therapy, inserting non-defective genes into cells taken from the patient and giving them back, have the advantage of not needing the tissue match required for standard transplants. Although not a standard treatment, this approach holds promise, especially for those in whom standard bone marrow transplantation has failed. Human Immunodeficiency Viruses/AIDS Although many viruses cause suppression of the immune system, only one wipes it
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