Putative neurosurgical transmission of Creutzfeldt-Jakob disease with analysis of donor and recipient: Agent strains

Comptes Rendus de l'Academie des Sciences - Serie III

Volumn 320, Issue 4, 1997, Pages 319-328

  El Hachimi, Khalid Hamid ^a   Chaunu, Marie Pierre ^b   Cervenakova, Larisa ^c   Brown, Paul ^c   Foncin, Jean François ^a  

^a PSL RESEARCH UNIVERSITY   (France)

^b REIMS UNIVERSITY HOSPITAL   (France)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

Creutzfeldt Jakob disease; Iatrogenic transmission; Immunohistopathology; PRNP gene; Strain agent

Indexed keywords

PRION PROTEIN;

ADULT; ARTICLE; ATAXIA; BRAIN; BRAIN CONTUSION; CASE REPORT; CODON; CREUTZFELDT JAKOB DISEASE; ELECTROENCEPHALOGRAM; FEMALE; GENETIC POLYMORPHISM; HUMAN; KURU; MALE; MOLECULAR GENETICS; NEUROSURGERY; NONHUMAN; PERIPHERAL NERVE; PRION; SKULL SURGERY; SPINAL CORD; VIRUS TRANSMISSION;

ATAXIA;

EID: 0030998170     PISSN: 07644469     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0764-4469(97)82774-6     Document Type: Article

References (27)

1. Prusiner S.B. 1982. Novel proteinaceous infectious particles cause scrapie, Science 216, 136-44
2. Brown P., Cathala F., Raubertas R., Gajdusek D.C., Castaigne P. 1986. Creutzfeldt-Jakob disease in France: epidemiologic data for the 15-year period 1968-1982. In: Unconventional Virus Diseases of the Central Nervous System (Court L.A., Dormont D., Brown P., Kingsbury D.T., eds), Editions CEA, Fontenay-aux Roses
3. Delasnerie-Lauprêtre N., Alpérovitch A. 1994. Epidémiologie de la maladie de Creutzfeldt-Jakob. Pathol. Biol. 43, 22-24
4. Brown P., Gibbs C.J., Rodgers-Johnson P., Asher D.M., Sulima M.P., Bacote A., Goldfarb L.G., Gajdusek D.C. 1994. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann. Neurol. 35, 513-529
5. Gibbs C.J., Gajdusek D.C., Asher D.M., Alpers M.P., Beck E., Daniel P.M., Matthews W.B. 1968. Creutzfeldt-Jakob disease (subacute spongiform encephalopathy): transmission to the chimpanzee. Science 161, 388-389
6. Will R.G., Ironside J.W., Zeidler M., Cousens S.N., Estibeiro K., Alpérovitch A., Poser S., Pocchiari M., Hofman A., Smith P.G. 1996. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 374, 921-925
7. Gajdusek D.C., Gibbs C.J., Alpers M. 1967. Transmission and passage of experimental 'kuru' to chimpanzees. Science 155, 212-214
8. Duffy P., Wolf J., Collins G., DeVoe A.G., Steeten B., Cowen D. 1974. Possible person-to-person transmission of Creutzfeldt-Jakob disease. New Engl. J. Med. 299, 692-693
9. Bernoulli C., Siegfried J., Baumgartner G., Regli F., Rabinowicz T., Gajdusek D.C., Gibbs C.J. 1977. Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery. Lancet 26, 478-479
10. Thodani V., Penar P.L., Partington J., Kalb R., Janssen R., Schonberger L.B., Rabkin C.S., Prichard J.W. 1988. Creutzfeldt-Jakob disease probably acquired from cadaveric dura mater graft, case report. J. Neurosurg. 69, 766-769
11. Kitamoto T, Shin R-W, Doh-Ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J. 1992. Abnormal isoform of prion proteins accumulates in the synoptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am. J. Pathol. 140, 1285-1294
12. Hauw J.-J., Gray F., Baudrimont M., Escourolle R. 1981. Cerebellar changes in 50 cases of Creutzfeldt-Jakob disease with emphasis on granule cell atrophy variant. Acta Neuropathol. Suppl. 7, 196-198
13. Billette de Villemeur T., Gourmelen M., Beauvais P., Rodriguez D., Vaudour G., Deslys J.-P., Dormont D., Richard P., Richardet J.-M. 1992. Maladie de Creutzfeldt-Jakob chez quatre enfants traités par hormone de croissance. Rev. Neurol. 148, 328-334
14. Brownell D., Oppenheimer D.R. 1965. An ataxic form of subacute presenile polioencephalopathy (Creutzfeldt-Jakob disease). J. Neurol. Neurosurg. Psychiatry 28, 350-361
15. Billette de Villemeur T., Gelort A., Deslys J.-P., Dormont D., Duyckaerts Ch., Jardin L., Dennit J., Robain O. 1994. Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study. Neuropathol. Appl. Neurobiol. 20, 111-117
16. Gajdusek D.C. 1992. Spontaneous generation of infectious nucleating amyloids in the transmissible and nontransmissible cerebral amyloidosis. Molecular Neurobiol. 8, 1-13
17. Dickinson A.G., Taylor D.M. 1978. Resistance of scrapie agent to decontamination. New Engl. J. Med. 299, 1413-1414
18. Brown P. Gibbs C.J., Amyx H.L., Kinsbury D.T., Rohwer R.G., Sulima M.P., Gajdusek D.C. 1982. Chemical desinfection of Creutzfeldt-Jakob virus. New Engl. J. Med. 315, 1279-1282
19. Ghetti B., Piccardo P., Spillantini M.G., Ichimiya Y., Porro M., Kitamoto T., Tateishi J., Seiler C., Frangione B., Bugiani O., Giaccone G., Prelli F., Goedert M., Dloughy S.R., Tagliavini F. 1996. Vascular variant of prion protein cerebral amyloidosis with Tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP. Proc. Natl. Acad. Sci. USA 93, 744-748
20. Allsop D., Ikeda S., Bruce M., Glenner G.G. 1988. Cerebrovascular amyloid in scrapie-affected sheep reacts with antibodies to prion protein. Neurosci. Lett. 92, 234-239
21. Foncin J.-F., Gaches J., Breton J. 1961. Maladie de Creutzfeldt-Jakob d'évolution aiguë. Rev. Neurol. 105, 66-69
22. Collinge J., Sidle K.C.L., Meads J., Ironside J., Hill A.F. 1996. Molecular analysis of prion strain variation and the aetiology of new variant CJD. Nature 383, 685-690
23. Collinge J., Palmer M.S., Dryden A.J. 1991. Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease. Lancet 337, 1441-1442
24. Palmer M.S., Dryden A.J., Hughes T., Collinge J. 1991. Homozygous prion protein genotype predisposes to sporadic Creutzfeld-Jakob disease. Nature 352, 340-342
25. Laplanche J.-L., Delasnerie-Lauprêtre N., Brandel J.-P., Chatelain J., Beaudry P., Alpérovitch A., Launay J.-M., 1994. Molecular genetics of prion disease in France. Neurology 44, 2347-2351
26. Deslys J.-P., Marce D., Dormont D. 1994. Similar genetic susceptibility in iatrogenic and sporadic Creutzfeltd-Jakob disease. J. Gen. Virol. 75, 23-27
27. Brown P., Cervenàkovà L., Goldfarb L.G., McCombie W.R., Rubenstein R., Will R.G., Pochiari M., Martinez-Lage J.F., Scalici C., Masullo C., Graupera G., Ligan J., Gajdusek D.C. 1994. Iatrogenic Creutzfeldt-Jakob disease: An example of interplay between ancient genes and modern medicine. Neurology 44, 291-293.