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level: Autoimmunity vs Autoimmune Disease

Questions and Answers List

level questions: Autoimmunity vs Autoimmune Disease

QuestionAnswer
What is autoimmunity?➢ Ehrlich used the term autoimmunity to signify an immune response against self. ➢ Over the years, autoimmunity has been recognized as not uncommon and not necessarily detrimental. ➢ All humans have many self-reactive antibodies in the blood but most show no sign of disease. ➢ Consequently the identification of autoantibodies is not a sufficient diagnostic tool for determining the presence of an autoimmune disorder ➢ There is a difference between an autoimmune response and disease: in the former case the autoantibodies do not cause dysfunction, but in the latter case they do. Autoimmunity may be asx, autoimmune diseases lead to inflammatory response and tissue injury
How is epidemiology of autoimmune diseases?➢ There are nearly 100 different forms of autoimmune disease, affecting up to 3 percent of the general population. ➢ Nearly any organ can be affected by either systemic or organ-specific autoimmune disease ➢ Women make up nearly 75 percent of all individuals afflicted by autoimmune disease, making these disorders one of the ten leading causes of death in women less than sixty-five years old. (may be hormonal) ➢ However, the female-to-male ratio varies widely among different diseases, being as high as 9:1 in SLE, Sjögren’s syndrome, and autoimmune thyroiditis and as low as 1:1 in vitiligo, TID, and Goodpasture’s syndrome Age of onset: some early childhood, some childbearing age, other later
What are some autoimmune diseases?SLE, RA, Sjogren, Scleroderma, Polymyositis (systemic) Hashimoto, Graves, Addisons, T1DM, Pemiphigus vulgaris, Bullous pemphigoid, vitiligo, good basture, MG, MS, Pernicious anemia, PBC, autoimmune hep (organ specific)
How is pathogenesis of autoimmune diseases?Genetic, environmental, Immune system malfunction and random factors all play a role in the pathogenesis of autoimmune diseases
What are types of autoimmunity? Acc to cell typeT cell (Like MS or AI encephalomyelitis, strength of T cell reactivation deteremines degree of parenchymal inflammation) B cell (autoantibodies, Like SLE, can be transmitted transplacentally [neonatal Grave's, congentital herat block, neonatal lupus], IgG antibodies cross placenta while IgM don't. half life of IgG 21-28 days so go to baby circulation in 6-12 months postpartum, mostly transient [exception is complete heart block mediated by anti-Ro/anti-La autoantibodies cross reacting w/cardiac antigens causing permenant inflammation and damage]. Usually several mechanisms [T cell and antibody tissue injury]
What are types of autoimmunity? Acc to organ affected?Systemic or organ specific Systemic (, such as SLE, involve multiple organs or tissues) Organ-specific ( involve a single organ or tissue, such as the thyroid gland in autoimmune thyroiditis or the islets of Langerhans in type I diabetes (TID)).
What are mechanisms of autoimmune tissue injury and examples?➢ Tissue damage in autoimmune diseases can occur through several mechanisms, which are analogous to three of the classical types of hypersensitivity reactions: Type II (caused by autoantibodies reactive with cell surface or matrix antigens), Type III (caused by immune complexes), and Type IV (delayed-type hypersensitivity, mediated by T cells). ➢ Autoimmune diseases differ from HS responses in that type I IgE-mediated responses do not seem to have a major role.
What are categories of immunopathologic responses?◦ Inactivation/activation antibody reactions ◦ Cytotoxic or cytolytic antibody reactions ◦ Immune-complex reactions ◦ Allergic reactions ◦ T-cell cytotoxic reactions ◦ Delayed HS reactions ◦ Granulomatous reactions ➢ This system accounts for the fact that multiple components of the immune system can be involved in various types of HS reactions
What is Gell and Coomb's classification of immunopathologic responses?➢ Gell and Coomb's classification has deficiencies but, with mechanism-based categories, it remains, overall, the simplest, most valid, and most logical way of distinguishing the host’s immune sensitivities. Type I, II, III and IV