The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
Prevalence of lymphoreticular prion protein accumulation in UK tissue samples
Abstract
This study aims to provide an estimate of the number of individuals in the UK who may be incubating variant Creutzfeldt‐Jakob disease and at risk of causing iatrogenic spread of the disease. Lymphoreticular accumulation of prion protein is a consistent feature of variant Creutzfeldt‐Jakob at autopsy and has also been demonstrated in the pre‐clinical phase. Immunohistochemical accumulation of prion protein in the lymphoreticular system remains the only technique that has been shown to predict neurological disease reliably in animal prion disorders. In this study, immunohistochemistry was used to demonstrate the presence of prion protein, with monoclonal antibodies KG9 and 3F4, in surgically removed tonsillectomy and appendicectomy specimens. The samples were collected from histopathology departments across the UK and anonymised prior to testing. Samples were tested from 16 703 patients (14 964 appendectomies, 1739 tonsillectomies), approximately 60% of whom were from the age group 20–29 years at operation. Twenty‐five per cent of the samples were excluded from the final analyses because they contained inadequate amounts of lymphoid tissue. Three appendicectomy samples showed lymphoreticular accumulation of prion protein, giving an estimated prevalence of 3/12 674 or 237 per million (95% CI 49–692 per million). The pattern of lymphoreticular accumulation in two of these samples was dissimilar from that seen in known cases of variant Creutzfeldt‐Jakob disease. Although it is uncertain whether immunohistochemical accumulation of prion protein in the lymphoreticular system is specific for variant Creutzfeldt‐Jakob disease, it has not been described in any other disease, including other forms of human prion disease or a range of inflammatory and infective conditions. These findings reinforce the importance of measures taken by the UK Department of Health to reduce the risk of spread of variant Creutzfeldt‐Jakob via blood products and surgical instruments, and of the urgency to proceed with large‐scale screening of fresh tonsil specimens for the presence of prion protein. Copyright © 2004 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A new variant of Creutzfeldt-Jakob disease in the UK
Will, R. G., Ironside, J. W., Zeidler, M., Estibeiro, K., Cousens, S. N., Smith, P. G., Alperovitch, A., Poser, S., Pocchiari, M., & Hofman, A. (1996) · The Lancet · doi:10.1016/s0140-6736(96)91412-9 · Cited by 2,707
Self-citationTransmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent
Bruce, M. E., Will, R. G., Ironside, J. W., McConnell, I., Drummond, D., Suttie, A., McCardle, L., Chree, A., Hope, J., Birkett, C., et al. (1997) · Nature · doi:10.1038/39057 · Cited by 1,967
Self-citationMolecular analysis of prion strain variation and the aetiology of 'new variant' CJD
Collinge, J., Sidle, K. C. L., Meads, J., Ironside, J., & Hill, A. F. (1996) · Nature · doi:10.1038/383685a0 · Cited by 1,735
Self-citationThe same prion strain causes vCJD and BSE
Hill, A. F., Desbruslais, M., Joiner, S., Sidle, K. C. L., Gowland, I., Collinge, J., Doey, L. J., & Lantos, P. (1997) · Nature · doi:10.1038/38925 · Cited by 1,456
Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion
Llewelyn, C., Hewitt, P., Knight, R., Amar, K., Cousens, S., Mackenzie, J., & Will, R. (2004) · The Lancet · doi:10.1016/s0140-6736(04)15486-x · Cited by 1,128
Brown, P., Gibbs, C. J., Rodgers‐Johnson, P., Asher, D. M., Sulima, M. P., Bacote, A., Goldfarb, L. G., & Gajdusek, D. C. (1994) · Annals of Neurology · doi:10.1002/ana.410350504 · Cited by 817
Hill, A., Butterworth, R., Joiner, S., Jackson, G., Rossor, M., Thomas, D., Frosh, A., Tolley, N., Bell, J., Spencer, M., et al. (1999) · The Lancet · doi:10.1016/s0140-6736(98)12075-5 · Cited by 699
Self-citationWadsworth, J., Joiner, S., Hill, A., Campbell, T., Desbruslais, M., Luthert, P., & Collinge, J. (2001) · The Lancet · doi:10.1016/s0140-6736(01)05403-4 · Cited by 693
Transmission dynamics and epidemiology of BSE in British cattle
Anderson, R. M., Donnelly, C. A., Ferguson, N. M., Woolhouse, M. E. J., Watt, C. J., Udy, H. J., MaWhinney, S., Dunstan, S. P., Southwood, T. R. E., Wilesmith, J. W., et al. (1996) · Nature · doi:10.1038/382779a0 · Cited by 600
Prion (PrPSc)-specific epitope defined by a monoclonal antibody
Korth, C., Stierli, B., Streit, P., Moser, M., Schaller, O., Fischer, R., Schulz-Schaeffer, W., Kretzschmar, H., Raeber, A., Braun, U., et al. (1997) · Nature · doi:10.1038/36337 · Cited by 567
Variant Creutzfeldt-Jakob disease
Collinge, J. (1999) · The Lancet · doi:10.1016/s0140-6736(99)05128-4 · Cited by 512
Transmission of prion diseases by blood transfusion
Hunter, N., Foster, J., Chong, A., McCutcheon, S., Parnham, D., Eaton, S., MacKenzie, C., & Houston, F. (2002) · Journal of General Virology · doi:10.1099/0022-1317-83-11-2897 · Cited by 508
Sabattini, E., Bisgaard, K., Ascani, S., Poggi, S., Piccioli, M., Ceccarelli, C., Pieri, F., Fraternali-Orcioni, G., & Pileri, S. A. (1998) · Journal of Clinical Pathology · doi:10.1136/jcp.51.7.506 · Cited by 461
Asante, E. A. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf653 · Cited by 357
"Friendly fire" in medicine: hormones, homografts, and Creutzfeldt-Jakob disease
BROWN, P. (1992) · The Lancet · doi:10.1016/0140-6736(92)92431-e · Cited by 350
Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease
Hilton, D. A., Fathers, E., Edwards, P., Ironside, J. W., & Zajicek, J. (1998) · The Lancet · doi:10.1016/s0140-6736(98)24035-9 · Cited by 344
Self-citationPathogenesis of Scrapie Virus Infection in the Mouse
Eklund, C. M., Kennedy, R. C., & Hadlow, W. J. (1967) · Journal of Infectious Diseases · doi:10.1093/infdis/117.1.15 · Cited by 343
Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt–Jakob Disease
Glatzel, M., Abela, E., Maissen, M., & Aguzzi, A. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa030351 · Cited by 336
Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues
Bruce, M., McConnell, I., Will, R., & Ironside, J. (2001) · The Lancet · doi:10.1016/s0140-6736(01)05411-3 · Cited by 255
Self-citationSurgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study
Collins, S., Law, M., Fletcher, A., Boyd, A., Kaldor, J., & Masters, C. (1999) · The Lancet · doi:10.1016/s0140-6736(98)08138-0 · Cited by 242
Valleron, A.-J., Boelle, P.-Y., Will, R., & Cesbron, J.-Y. (2001) · Science · doi:10.1126/science.1066838 · Cited by 240
Predicting the CJD epidemic in humans
Cousens, S. N., Vynnycky, E., Zeidler, M., Will, R. G., & Smith, P. G. (1997) · Nature · doi:10.1038/385197a0 · Cited by 214
Selective expression of prion protein in peripheral tissues of the adult mouse
Ford, M. J., Burton, L. J., Morris, R. J., & Hall, S. M. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00155-0 · Cited by 213
Pathogenesis of scrapie in mice after intragastric infection
Kimberlin, R. H., & Walker, C. A. (1989) · Virus Research · doi:10.1016/0168-1702(89)90040-3 · Cited by 212
Identification of multiple quantitative trait loci linked to prion disease incubation period in mice
Lloyd, S. E., Onwuazor, O. N., Beck, J. A., Mallinson, G., Farrall, M., Targonski, P., Collinge, J., & Fisher, E. M. C. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.101130398 · Cited by 192
Predicted vCJD mortality in Great Britain
Ghani, A. C., Ferguson, N. M., Donnelly, C. A., & Anderson, R. M. (2000) · Nature · doi:10.1038/35020688 · Cited by 186
Self-citationPeripheral Tissue Involvement in Sporadic, Iatrogenic, and Variant Creutzfeldt-Jakob Disease
Head, M. W., Ritchie, D., Smith, N., McLoughlin, V., Nailon, W., Samad, S., Masson, S., Bishop, M., McCardle, L., & Ironside, J. W. (2004) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63105-7 · Cited by 170
Self-citationRace, R., Raines, A., Raymond, G. J., Caughey, B., & Chesebro, B. (2001) · Journal of Virology · doi:10.1128/jvi.75.21.10106-10112.2001 · Cited by 167
Accumulation of prion protein in tonsil and appendix: review of tissue samples
Hilton, D. A., Ghani, A. C., Conyers, L., Edwards, P., McCardle, L., Penney, M., Ritchie, D., & Ironside, J. W. (2002) · BMJ · doi:10.1136/bmj.325.7365.633 · Cited by 142
Self-citationPreclinical test for prion diseases
Schreuder, B. E. C., van Keulen, L. J. M., Vromans, M. E. W., Langeveld, J., & Smits, M. A. (1996) · Nature · doi:10.1038/381563a0 · Cited by 136
Predictability of the UK Variant Creutzfeldt-Jakob Disease Epidemic
d’Aignaux, J. H., Cousens, S., & Smith, P. G. (2001) · Science · doi:10.1126/science.1064748 · Cited by 124
Sporadic Creutzfeldt–Jakob disease and surgery: A case–control study using community controls
Ward, H. J. T., Everington, D., Croes, E. A., Alperovitch, A., Delasnerie–Lauprêtre, N., Zerr, I., Poser, S., & van Duijn, C. M. (2002) · Neurology · doi:10.1212/wnl.59.4.543 · Cited by 95
Updated projections of future vCJD deaths in the UK
Ghani, A. C., Donnelly, C. A., Ferguson, N. M., & Anderson, R. M. (2003) · BMC Infectious Diseases · doi:10.1186/1471-2334-3-4 · Cited by 92
Self-citationPathological diagnosis of variant Creutzfeldt‐Jakob disease
Ironside, J. W., McCardle, L., Horsburgh, A., Lim, Z., & Head, M. W. (2002) · Apmis · doi:10.1034/j.1600-0463.2002.100110.x · Cited by 77
Self-citationSpecificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt–Jakob disease
Hilton, D. A., Sutak, J., Smith, M., Penney, M., Conyers, L., Edwards, P., McCardle, L., Ritchie, D. L., Head, M. W., Wiley, C. A., et al. (2004) · Journal of Clinical Pathology · doi:10.1136/jcp.2003.012278 · Cited by 71
Self-citationKovács, G. G., Lindeck‐Pozza, E., Chimelli, L. M. C., Araújo, A., Gabbai, A. A., Ströbel, T., Glatzel, M., Aguzzi, A., & Budka, H. (2003) · Annals of Neurology · doi:10.1002/ana.10813 · Cited by 56
Hilton, D. A. (2000) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.2000.00281.x · Cited by 22
Self-citationParchi, P., Giese, A., Capellari, S., Brown, P., Schulz-Schaeffer, W., Windl, O., Zerr, I., Budka, H., Kopp, N., Piccardo, P., et al. (1999) · Annals of Neurology · doi:10.1002/1531-8249(199908)46:2<224::aid-ana12>3.0.co;2-w
Cited by
Vamvakas, E. C., & Blajchman, M. A. (2009) · Blood · doi:10.1182/blood-2008-10-167643 · Cited by 621
Lin, S.-M., Lin, C.-J., Lin, C.-C., Hsu, C.-W., & Chen, Y.-C. (2005) · Gut · doi:10.1136/gut.2004.045203 · Cited by 592
Gill, O. N., Spencer, Y., Richard-Loendt, A., Kelly, C., Dabaghian, R., Boyes, L., Linehan, J., Simmons, M., Webb, P., Bellerby, P., et al. (2013) · BMJ · doi:10.1136/bmj.f5675 · Cited by 300
Self-citationUttley, L., Carroll, C., Wong, R., Hilton, D. A., & Stevenson, M. (2020) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(19)30615-2 · Cited by 258
Self-citationInnate Immune Tolerance in Microglia Does Not Impact on Central Nervous System Prion Disease
Pal, R., Bradford, B. M., & Mabbott, N. A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.918883 · Cited by 7
Metadata
- Authors
- Hilton, D. A., Ghani, A. C., Conyers, L., Edwards, P., McCardle, L., Ritchie, D., Penney, M., Hegazy, D., & Ironside, J. W.
- Venue
- The Journal of Pathology
- Publisher
- Wiley
- Published
- 2004-05-21
- Volume
- 203
- Issue
- 3
- Pages
- 733-739
- ISSN
- 0022-3417 (ISSN-L)
- 1096-9896
- OpenAlex
- W2045562971
- Cited by
- 444
- References
- 38
- FWCI
- 15.64
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.