Transmissible spongiform encephalopathy
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Transmissible spongiform encephalopathy Microchapters |
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Differentiating Transmissible spongiform encephalopathy from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Kiran Singh, M.D. [2] Rinky Agnes Botleroo, M.B.B.S.
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Synonyms and keywords: TSE; prion diseases
Overview
Historical Perspective
- Natural Scrapie is a infection that affects sheep and is caused by an unusual infectious agent.It was first described in 1732.
- Kuru is the first prion disease in humans which was described in 1957.It is a fatal exotic neurodegenerative disease that affects only people of a single language group in the remote mountainous interior of New Guinea.
- In 1959, veterinary pathologist W.J. Hadlow first recognized several similarities between Scrapie and Kuru, which is a fatal exotic neurodegenerative disease that affects only people of a single language group in the remote mountainous interior of New Guinea.
- In 1959, I. Klatzo also noted that Kuru's histopathology resembled that of Creutzfeldt-Jakob disease (CJD), another fatal neurodegenerative progressive disease of unknown etiology that A.M. Jakob had first described in 1921.
- Gajdusek, C.J. Gibbs, Jr., and M.P. Alpers used the existing knowledge of Scrapie and started efforts to transmit Kuru by inoculating Kuru brain tissue into non-human primates, that-although requiring several years-ultimately proved successful in 1965.Later Gajdusek and colleagues went on to demonstrate that not only the more common sporadic form of CJD but also familial CJD and a generally similar familial brain disease (Gerstmann-Sträussler-Scheinker syndrome) were also transmissible, first to non-human primates and later to other animals.
- In 1982, Stanley B. Prusiner formulated "prion hypothesis". Prusiner recognized that a misfolded form of a ubiquitous normal host protein was usually (if not always) detectable in tissues containing TSE agents, greatly facilitating the diagnosis and understanding their pathogenesis. Prusiner proposed that the TSE agent was likely to be composed partly (if not entirely )of the abnormal protein, for which he used the term "prion" protein and "prion" for the agent. Expression of the prion protein by animals-while not essential for life-was later found to be obligatory to infect them with TSEs
Pathophysiology
Causes
Differentiating Transmissible spongiform encephalopathy from other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications and Prognosis
Major or Mild Neurocognitive Disorder Due to Prion Disease
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Primary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
References
- This entry incorporates public domain text originally from the National Institute of Neurological Disorders and Stroke, National Institutes of Health [3] and the U.S. National Library of Medicine [4]
- Brown P, Preece M, Brandel JP, Sato T, McShane L, Zerr I, Fletcher A, Will RG, Pocchiari M, Cashman NR, d'Aignaux JH, Cervenakova L, Fradkin J, Schonberger LB, Collins SJ (2000). "Iatrogenic Creutzfeldt-Jakob disease at the millennium". Neurology. 55 (8): 1075–81. PMID 11071481.
- Montagna P, Gambetti P, Cortelli P, Lugaresi E (2003). "Familial and sporadic fatal insomnia". Lancet Neurol. 2 (3): 167–76. PMID 12849238.
- Prusiner SB (2001). "Shattuck lecture--neurodegenerative diseases and prions". N Engl J Med. 344 (20): 1516–26. PMID 11357156.
- Weissmann C (2004). "The state of the prion". Nat Rev Microbiol. 2 (11): 861–71. PMID 15494743.
External Links
- Transmissible Spongiform Encephalopathy
- Neurodegenerative Disease.
- Neurodegenerative disease: Encephalopathy.
- American Symposium
cs:Transmisivní spongiformní encefalopatie da:TSE de:Transmissible spongiforme Enzephalopathie ko:프리온 질병 simple:Prion disease