Literature DB >> 14990604

Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob disease.

D A Hilton1, J Sutak, M E F Smith, M Penney, L Conyers, P Edwards, L McCardle, D Ritchie, M W Head, C A Wiley, J W Ironside.   

Abstract

BACKGROUND: Immunocytochemical accumulation of prion protein (PrP) in lymphoid tissues is a feature of variant Creutzfeldt-Jakob disease (vCJD) that has been used both to aid in the diagnosis of patients and as a basis of large scale screening studies to assess the prevalence of preclinical disease in the UK. However, the specificity of this approach is unknown. AIM: To assess the specificity of lymphoreticular accumulation of PrP for vCJD by examining a range of human diseases.
METHODS: Paraffin wax embedded lymphoreticular tissues from patients with several reactive conditions (58 cases), tumours (27 cases), vCJD (54 cases), and other human prion diseases (56 cases) were assessed. PrP accumulation was assessed by immunocytochemistry using two different monoclonal anti-PrP antibodies and a sensitive detection system.
RESULTS: All cases of vCJD showed widespread lymphoreticular accumulation of PrP; however, this was not seen in the other conditions examined.
CONCLUSION: Lymphoreticular accumulation of PrP, as assessed by immunocytochemistry, appears to be a highly specific feature of vCJD.

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Year:  2004        PMID: 14990604      PMCID: PMC1770247          DOI: 10.1136/jcp.2003.012278

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  23 in total

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Authors:  D A Hilton
Journal:  Neuropathol Appl Neurobiol       Date:  2000-10       Impact factor: 8.090

Review 2.  Laboratory diagnosis of variant Creutzfeldt-Jakob disease.

Authors:  J W Ironside; M W Head; J E Bell; L McCardle; R G Will
Journal:  Histopathology       Date:  2000-07       Impact factor: 5.087

3.  Retrospective study of prion-protein accumulation in tonsil and appendix tissues.

Authors:  J W Ironside; D A Hilton; A Ghani; N J Johnston; L Conyers; L M McCardle; D Best
Journal:  Lancet       Date:  2000-05-13       Impact factor: 79.321

4.  Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues.

Authors:  M E Bruce; I McConnell; R G Will; J W Ironside
Journal:  Lancet       Date:  2001-07-21       Impact factor: 79.321

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Journal:  Vet Rec       Date:  2001-04-07       Impact factor: 2.695

6.  Early accumulation of pathological PrP in the enteric nervous system and gut-associated lymphoid tissue of hamsters orally infected with scrapie.

Authors:  M Beekes; P A McBride
Journal:  Neurosci Lett       Date:  2000-01-14       Impact factor: 3.046

7.  Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay.

Authors:  J D Wadsworth; S Joiner; A F Hill; T A Campbell; M Desbruslais; P J Luthert; J Collinge
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9.  Possible underascertainment of variant Creutzfeldt-Jakob disease: a systematic study.

Authors:  C E M Hillier; R L Salmon; J W Neal; D A Hilton
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Authors:  A F Hill; R J Butterworth; S Joiner; G Jackson; M N Rossor; D J Thomas; A Frosh; N Tolley; J E Bell; M Spencer; A King; S Al-Sarraj; J W Ironside; P L Lantos; J Collinge
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  20 in total

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2.  Clearance and prevention of prion infection in cell culture by anti-PrP antibodies.

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Review 4.  Immunotherapy in prion disease.

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6.  Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice.

Authors:  Jonathan D F Wadsworth; Susan Joiner; Jacqueline M Linehan; Melanie Desbruslais; Katie Fox; Sharon Cooper; Sabrina Cronier; Emmanuel A Asante; Simon Mead; Sebastian Brandner; Andrew F Hill; John Collinge
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-03       Impact factor: 11.205

7.  Persistent propagation of variant Creutzfeldt-Jakob disease agent in murine spleen stromal cell culture with features of mesenchymal stem cells.

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9.  Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.

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10.  Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey.

Authors:  Jonathan P Clewley; Carole M Kelly; Nick Andrews; Kelly Vogliqi; Gary Mallinson; Maria Kaisar; David A Hilton; James W Ironside; Philip Edwards; Linda M McCardle; Diane L Ritchie; Reza Dabaghian; Helen E Ambrose; O Noel Gill
Journal:  BMJ       Date:  2009-05-21
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