Review: Creutzfeldt-Jakob disease

Brain Pathology

Volumn 6, Issue 4, 1996, Pages 379-388

  Ironside, J W ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL TISSUE; BRAIN SPONGIOSIS; CREUTZFELDT JAKOB DISEASE; DISEASE TRANSMISSION; HISTOCHEMISTRY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MONKEY; NONHUMAN; PRION DISEASE; REVIEW;

EID: 0029910951     PISSN: 10156305     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1750-3639.1996.tb00869.x     Document Type: Review

References (83)

1. Amouyel P, Vidai O, Launay JM, Laplanche JL (1994) The apolipoprotein E alleles as major susceptibility factors for Creutzfeldt-Jakob disease. Lancet 344: 1315-1318
2. Anonymous Editorial (1990) Prion disease - spongiform encephalopathies unveiled. Lancet 336. 21-22
3. Baker HF, Ridley RM (1992) The genetics and transmissibility of human spongiform encephalopathy. Neurodegen 1: 3-16
4. Baker HF, Ridley RM, Duchen LW, Crow TJ, Bruton CJ (1994) Induction of beta(A4)-amyloid in primates by injection of Alzheimer's disease brain homogenate: comparison with transmission of spongiform encephalopathy. Mol Neurobiol 8: 25-39
5. Barcikowska M, Liberski PP, Boellaard JW, Brown P, Gajdusek DC, Budka H (1993) Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler syndrome. Acta Neuropathol 85: 623-627
6. Bastian FO (1991) Creutzfeldt-Jakob disease and other transmissible human spongiform encephalopathies. Mosby Year Book: St Louis
7. Bateman D, Hilton D, Love S, Zeidler M, Beck J, Collinge J (1995) Sporadic Creutzfeldt-Jakob disease in a 18-year old in the UK. Lancet 346. 1155-1156
8. Bell JE, Ironside JW (1993) How to tackle a possible Creutzfeldt-Jakob disease necropsy J Clin Pathol 46: 193-197
9. Bell JE, Ironside JW (1993) Neuropathology of spongiform encephalopathies in humans. Brit Med Bull 49: 738-777
10. Berman P, Davidson GS, Becker LE (1988) Progressive neurological deterioration in a 14-year-old girl. Pediatr Neurosci 14: 42-49
11. Billette de Villemeur T, Gellott A, Deslys JP, Dormont D, Duyckaerts CH, Jardin L, Dennr J, Robain O (1994) latrogenic Creutzfeldt-Jakob disease in three growth hormone recipients, a neuropathological study. Neuropathol Appl Neurobiol 20. 111-117
12. Boellaard JW, Doerr-Schott J, Scholte W (1993) Miniplaques and shapeless cerebral amyloid deposits in a case of Gerstmann-Sträussler-Scheinker's syndrome. Acta Neuropathol 86. 532-535
13. Bortone E, Bettoni L, Giorgi C, Terzano MG, Trabattoni GR, Mancia D (1994) Reliability of EEG in the diagnosis of Creutzfeldt-Jakob disease. Electroenceph Clin Neurophysiol 90 323-330
14. Britton TC, Al-Sarraj S, Shaw C,Campbell T, Collinge J (1995) Sporadic Creutzfeldt-Jakob disease in a 16-year old in the UK Lancet 346 1155
15. Brown P, Cathala F, Castaigne P, Gajdusek DC (1986) Creutzfeldt-Jakob disease clinical analysis of a consecutive series of 230 neuropathologically verified cases Ann Neurol 20. 597-602
16. Brown P, Cathala F, Labauge R, Pages M, Alary JC, Baron H (1985) Epidemiologic implications of Creutzfeldt-Jakob disease in a 19-year old girl. Europ J Epid 1. 42-47
17. Brown P, Cathala F, Roberts RF, Gajdusek DC, Cataigne P (1987) The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature. Neurology 37: 895-904
18. Brown P, Crevenakova L Boellaard JW Stavrou D Goldfarb LG Gajdusek DC (1994) Identification of a PRNP gene mutation in Jakob's original Creutzfeldt-Jakob disease family. Lancet 344 130-131
19. Brown P, Gibbs Jnr CJ, Rodgers-Jackson P, Asher DM, Sulima MP, Bacote A, Goldfarb LG, Gajdusek DC (1994) Human spongiform encephalopathy: The National Institute of Health series of 300 cases of experimentally transmitted disease. Ann Neurol 35: 513-529
20. Brown P, Kaur P, Sulima M, Goldfarb LG, Gibbs Jnr CJ, Gajdusek DC (1993) Real and imagined clinicopathological limits of "prion dementia". Lancet 341: 127-129
21. Brown P, Preece MA, Will RG (1992) "Friendly fire in medicine: hormones homografts and Creutzfeldt-Jakob disease. Lancet 340: 24-27
22. Brown P, Rodgers-Johnson P, Cathala F, Gibbs Jnr CJ, Gajdusek DC (1984) Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility and differential diagnosis. Ann Neurol 16. 295-304
23. Bruce ME (1996) Strain typing studies of scrapie and BSE. In: Prion Diseases, Baker HF, Ridley RM (eds), Chapter 13, pp 223-236, Humana Press , New Jersey
24. Budka H, Aguzzi A, Brown P, Brucher J-M, Bugiani O, Gullota F, Haltia M, Hauw J-J, Ironside JW, Jeltinger K, Kretzschmar HA, Lantos PL, Masullo C, Scholte W, Tateishi J, Weller RO (1995) Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 5: 459-466
25. Bugiani O, Giaccone G, Verga L, Pollo B, Frangione B, Farlow MR, Tagliavini F, Ghetti B (1993) βPP participates in PrP-amyloid plaques of Gerstmann-Straussler-Scheinker disease, Indiana kindred. J Neuropathol Exp Neurol 52. 66-70
26. Carlson GA, Ebeling C, Yang S-L, Telling G, Torchia M, Groth D, Westaway D, DeArmond SJ, Prusiner SB (1994) Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice. Proc Nat Acad Sci USA 91: 5690-5694
27. Chazot G, Broussolle E, Lapras CL, Kopp N (1996) New variant of Creutzfeldt-Jakob disease in a 26-year-old French man Lancet 347: 1181-1182
28. Collinge J, Owen F, Poulter M, Leach M, Crow TJ, Rossor MN, Hardy J, Mullan MJ, Janota I, Lantos PL (1990) Prion dementia without characteristic pathology. Lancet 1336: 7-9
29. Collinge J, Palmer MS, Dryden AJ (1991) Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease. Lancet 337. 1441-1142
30. Collinge J, Whittington MA, Sidle KCL, Smith CJ, Palmer MS, Clarke AR, Jefferys JGR (1994) Prion protein is necessary for normal synaptic function. Nature 370 295-297
31. Come JH, Fraser PE, Lansbury Jnr PT (1993) A kinetic model for amyloid formation in the prion diseases: Importance of seeding. Proc Nat Acad Sci USA 90: 5959-5963
32. Creutzfeldt HG (1920) Uber eine eigenartige herdformige Erkrankung des Zentralnervensystems. Z ges Neurol Psychiat 57: 1-18
33. de Silva R, Ironside JW, McCardle L, Esmonde TFG, Bell JE, Will RG, (1994) Neuropathological phenotype and "prion protein" genotype correlation in sporadic Creutzfeldt-Jakob disease. Neurosci Lett 179. 50-52
34. DeArmond SJ (1993) Alzheimer's disease and Creutzfeldt-Jakob disease: overlap of pathogenic mechanisms. Curr Opin Neurol 6: 872-881
35. DeArmond S, Yang SL, Gayetano-Canlas J, Groth D, Prusiner S (1994) The neuropathological phenotype in transgenic mice expressing different prion protein constructs. Phil Trans R Soc Lond 343: 415-423
36. Delasnerie-Laupretre N, Poser S, Pocchiari M (1995) Incidence of Creutzfeldt-Jakob disease in Europe Lancet 346 898
37. Deslys J-P, Lasmézas C, Dormont D (1994) Selection of specific strains in iatrogenic Creutzfeldt-Jakob disease Lancet 343. 848-849.
38. Diringer H (1995) Proposed link between transmissible spongiform encephalopathies of man and animals. Lancet 344. 1208-1210
39. Fraser H, Brown K (1994) Peripheral pathogenesis of scrapie in normal and immunocompromised mice. Animal Technol 45: 21-23
40. Gibbs CJ, Gajdusek DC, Asher DM, Alpers MP, Beck E, Daniel PM, Matthews WB (1968) Creutzfeldt-Jskob disease (subacute spongiform encephalopathy): Transmission to the chimpanzee. Science 161: 388-389
41. Goldfarb LG, Brown P, Cervenakova L, Gajdusek DC (1994) Molecular genetic studies of Creutzfeldt-Jakob disease. Mol Neurobiol 8. 89-97
42. Goodbrand IA, Ironside JW, Nicolson D, Bell JE (1995) Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldt-Jakob disease. Neurosci Lett 183: 127-130
43. Hainfellner JA, Brantner-Inthaler S, Cercenakova L, Brown P, Kitamoto T, Tateishi J, Diringer H, Liberski PP, Regele H, Feucht M, Mayr N, Wessely P, Summer K, Seitelberger F, Budka H (1995) The original Gerstmann-Straussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype Brain Pathol 5: 201-213
44. Hansen LA, Masliah E, Terry RD, Mirra SS (1989) A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change. Acta Neuropathol 78: 194-201
45. Hayward PAR, Bell JE, Ironside JW (1994) Prion protein immunocytochemistry: The development of reliable protocols for the investigation of Creutzfeldt-Jakob disease. Neuropathol Appl Neurobiol 20: 375-383
46. Jakob A (1921) Uber eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswertem anatomichen Befunde (Spastische Pseudosklerose-Encephalomyelopathie mit disseminierten Degenerations-herden). Z ges Neurol Psychiat 64: 147-228
47. Jarrett JT, Lansbury Jnr PT (1993) Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie? Cell 73: 1055-1058
48. Kimberlin RH (1994) Transmissible encephalopathies in animals Can J Vet Res 54: 30-37
49. Kitamoto T, Shin RW, Doh-ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J (1992) Abnormal isoform of prion protein accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob Disease Am J Pathol 140 1285-1289
50. Kitamoto T, Tateishi J (1988) Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies Am J Pathol 131 435-443
51. Klatzo I, Gajdusek DC, Vigas V ( 1959) Pathology of kuru Lab Invest 8: 799-847
52. Kretzschmar HA, Ironside JW, DeArmond SJ, Tateishi J (in press) Diagnostic criteria for sporadic Creutzfeldt-Jakob disease Arch Neurol
53. Kulczycki J, Jedrzejowska H, Gajkowski K, Tarnowska-Dzidusko E, Lojkowska W (1991) Creutzfeldt-Jakob disease in young people. Europ J Epid 7: 501-504
54. Lantos PL (1992) From slow virus to prion: a review of transmissible spongiform encephalopathies. Histopathology 20 1-11
55. Lasmézas CI, Deslys J-P, Demalmay R, Adjou KT, Lamoury F, Dormont D, Robain O, Ironside JW, Hauw J-J (1996) BSE transmission to macaques. Nature 381: 743-744
56. MacDonald ST, Sutherland K, Ironside JW (1996) Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease. Neuropathol Appl Neurobiol 22: 285-292
57. Manuelidis EE, Rorke LB (1989) Transmission of Alpers' disease (chronic progressive encephalopathy) produces experimental Creutzfeldt-Jakob disease in hamsters. Neurology 39: 615-621
58. Martinez-Lage JF, Poza M, Sola J, Tortosa JG, Brown P, Crevenakova L, Esteban JA, Mendoza A (1994) Accidental transmission of Creutzfeldt-Jakob disease by dural cadaveric grafts. J Neurol Neurosurg Psych 57. 1091-1904
59. Masters CL, Harris JO, Gajdusek DC,Gibbs CJ Jnr, Bernoulli C, Asher DM (1979) Creutzfeldt-Jakob disease, patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol 5: 177-188
60. Meiner Z, Halimi M, Polakiewicz RD, Prusiner SB, Gabizon R (1992) Presence of prion protein in peripheral tissues of Libyan Jews with Cretuzfeldt-Jakob disease. Neurology 42: 1355-1360
61. Ministry of Agriculture, Fisheries and Food (1996) Bovine Spongiform Encephalopathy in Great Britain A Progress Report. London
62. Miyazono M, Iwaki T, Kitamoto T, Kaneko Y, Doh-ura K, Tateishi J (1991) A comparative Immunohistochemical study of kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation. Am J Pathol 139: 589-598
63. Miyazono M, Kitamoto T, Iwaki T, Tateishi J (1992) Colocalization of prion protein and A4/β protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome. Acta Neuropathol 83: 333-339
64. Monreal J, Collinge GH , Masters CL, Miller Fisher C, Ronald CK, Gibbs Jnr CJ , Gajdusek D C (1981) Creutzfeldt-Jakob disease in an adolescent. J Neurol Sci 52: 341-350
65. Mori S, Hamada C, Kumanishi T, Fukuhara N, Ichihashi Y, Ikuta F, Miyatake T, Tsubaki T (1989) A Creutzfeldt-Jakob disease agent (Echigo-1 strain) recovered from brain tissue showing the "panencephalopathic type" disease Neurology 39 1337-1342
66. Nakagawa Y, Kitamoto T, Furukawa H, Ogomori K, Tateishi J (1995) Apolipoprotein E in Creutzfeldt-Jakob disease. Lancet 345: 68-69
67. Packer RJ, Cornblath DR, Gonatas NK, Bruno LA , Asbury AK (1980) Creutzfeldt-Jakob disease in a 20-year old woman. Neurology 30: 492-496
68. Palmer MS, Dryden AJ, Hughes JT, Collinge J (1991) Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 352: 340-342
69. Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AAF, Trojanowski JQ, Petersen RB, Gambetti P (1996) Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 39: 669-680
70. Pickering-Brown SM, Mann DMA, Owen F, Ironside JW, de Silva R, Roberts DA, Balderson DJ, Cooper PN (1995) Allelic variations in apolipoprotein E and prion protein genotype related to plaque formation and age of onset in sporadic Creutzfeldt-Jakob disease. Neurosci Lett 187: 127-129
71. Price DL, Borchell DR, Sisodia S (1993) Alzheimer disease and the prion disorders: amyloid β-protein and prion protein amyloidoses. Proc Nat Acad Sci USA 90: 6381-6384
72. Prusiner SB (1993) Genetic and infectious prion diseases. Arch Neurol 50: 1129-1153
73. Prusiner S B (1994) Biology and genetics of prion disease. Ann Rev Microbiol 48: 655-686
74. CJD in the nervous system. Brain Pathol 5: 33-41
75. Sutherland K, Macdonald ST, Ironside JW (1996) Quantification and analysis of the neuropathological features of Creutzfeldt-Jakob disease. J Neurosci Meth 64: 123-132
76. Taraboulos A, Jendroska K, Serban D, Yang S-L, DeArmond SJ, Prusiner SB (1992) Regional mapping of prion proteins in brain. Proc Natl Acad Sci USA 89: 7620-7624
77. The National CJD Surveillance Unit and the Department of Epidemiology and Population Sciences London School of Hygiene and Tropical Medicine (1995) Creutzfeldt-Jakob Disease Surveillance in the United Kingdom: Fourth Annual Report. Edinburgh
78. van Keulen LJM, Schreuder BEC, Meloen RH, Mooij-Harkes G, Vromans MEW, Langeveld JPM (1996) Immunohistochemical detection of prion protein in lymphoid tissues of sheep with natural scrapie. J Clin Microbiol 34: 1228-1231
79. Weller RO, Steart V , Powell-Jackson JD (1986) Pathology of Creutzfeldt-Jakob disease associated with pituitary-derived human growth hormone administration. Neuropathol Appl Neurobiol 12. 117-129
80. Wells GAH, Scott AC, Johnson CT, Gunning R F, Hancock R D, Jeffrey M, Dawson M, Bradley R (1987) A novel progressive spongiform encephalopathy in cattle. Vet Rec 121: 419-420
81. Will RG (1993) Epidemiology of Creutzfeldt-Jakob disease. Brit Med Bull 49: 960-970
82. Will RG (1996) Surveillance of prion diseases in humans. In Prion Diseases, Baker HF, Ridley RM (eds.), Chapter 7, pp 119-137, Humana Press : New Jersey
83. Will RG, Ironside JW, Zeidler M, Cousens S, Estebeiro K, Alperovitch A, Poser S, Pocchiari M, Hofman A, Smith PG (1996) A new variant of Creutzfeldt-Jakob disease in the UK Lancet 347: 921-925