Evidence map›Paper›PMID 28518033›Full record

ArticleEmerging infectious diseases2017

Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients.

Jean Y Douet, Caroline Lacroux, Naima Aron, Mark W Head, Séverine Lugan, Cécile Tillier, Alvina Huor, Hervé Cassard, Mark Arnold, Vincent Beringue and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Emerging infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Diagnosis of Prion Diseases.Sub-cellular biochemistry · 2025
    Review
  7. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2024
    Article
  8. Article
  9. Article
  10. Variant CJD: Reflections a Quarter of a Century on.Pathogens (Basel, Switzerland) · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. The emergence of classical BSE from atypical/Nor98 scrapie.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  18. PMCA-replicated PrPScientific reports · 2019
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 2 countries.

Jean Y Douet
Caroline Lacroux
Naima Aron
Mark W Head
Séverine Lugan
Cécile Tillier
Alvina Huor
Hervé Cassard
Mark Arnold
Vincent Beringue
James W Ironside
Olivier Andréoletti
Interaction Hôtes Agents Pathogènes · FRAnimal and Plant Health Agency · GBEdinburgh College · GBUniversity of Edinburgh · GBVirologie et Immunologie Moléculaires · FR

Funding

Medical Research Council G0600953Medical Research Council G0900580Medical Research Council MR/L016400/1
6 · The paper itself

Abstract

In the United-Kingdom, ≈1 of 2,000 persons could be infected with variant Creutzfeldt-Jakob disease (vCJD). Therefore, risk of transmission of vCJD by medical procedures remains a major concern for public health authorities. In this study, we used in vitro amplification of prions by protein misfolding cyclic amplification (PMCA) to estimate distribution and level of the vCJD agent in 21 tissues from 4 patients who died of clinical vCJD and from 1 asymptomatic person with vCJD. PMCA identified major levels of vCJD prions in a range of tissues, including liver, salivary gland, kidney, lung, and bone marrow. Bioassays confirmed that the quantitative estimate of levels of vCJD prion accumulation provided by PMCA are indicative of vCJD infectivity levels in tissues. Findings provide critical data for the design of measures to minimize risk for iatrogenic transmission of vCJD.

Indexed as

Biological AssayAnimalsAsymptomatic DiseasesBone MarrowCreutzfeldt-Jakob SyndromeFemaleHumansKidneyLiverLungMaleMiceProtein FoldingPrPC ProteinsSalivary GlandsUnited KingdomPrPC Proteinsasymptomatic patientsclinical patientsCreutzfeldt-Jakob diseaseintracerebral inoculationmeningitis/encephalitisprions and related diseasesprotein misfolding cyclic amplificationpublic healthScotlandtissuesUnited Kingdomvariant Creutzfeldt-Jakob diseasevariant Creutzfeldt-Jakob disease prionsvariant infectivityvCJD

Identifiers

PMID28518033
PMCPMC5443438
OpenAlexW2606061345

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.