Evidence map›Paper›PMID 15331720›Full record

ArticleJournal of virology2004

Coxsackievirus B4 infection of human fetal thymus cells.

Fabienne Brilot, Vincent Geenen, Didier Hober, Cheryl A Stoddart

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Assessment of Thymic Output Dynamics AfterFrontiers in immunology · 2020
    Article
  9. In-utero coxsackievirus B4 infection of the mouse thymus.Clinical and experimental immunology · 2017
    Article
  10. Review
  11. Review
  12. Genetic-epigenetic dysregulation of thymic TSH receptor gene expression triggers thyroid autoimmunity.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  13. Review
  14. Review
  15. Viral infections and molecular mimicry in type 1 diabetes.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2012
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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

4 authors at 4 institutions in 3 countries.

Fabienne BrilotGladstone Institute of Virology and Immunology, University of California, San Francisco, USA.
Vincent Geenen
Didier Hober
Cheryl A Stoddart
Gladstone Institutes · USUniversité de Lille · FRUniversity of California, San Francisco · USUniversity of Liège · BE

Funding

TISSUE-BASED SMALL ANIMAL MODEL FOR HIV DRUG DISCOVERYN01AI005418 · NIAID · J. DAVID GLADSTONE INSTITUTES · PI STODDART, CHERYL · 2000 to 2000
$971k
NIAID NIH HHS N01 AI005418
6 · The paper itself

Abstract

The infection of human fetal thymus organ cultures (FTOC) with coxsackievirus B4 E2 (CVB4 E2) was investigated. Both positive- and negative-strand viral RNA were detected by real-time quantitative reverse transcription-PCR (RT-PCR) in CVB4 E2-infected FTOC, which supported high yields of virus production (approximately 10(6) 50% tissue culture infective doses/ml), and in flow-sorted thymocyte populations for 7 days after inoculation. Cortical CD4+ CD8+ thymocytes were found to be the principal targets of infection. Inoculation of human FTOC with CVB4 E2 led to a marked and progressive depletion of immature thymocytes (CD4+ CD8+ cells) with no enhancement of Annexin V-positive cells. CVB4 E2 replication caused significant major histocompatibility complex (MHC) class I upregulation on these cells. MHC class I upregulation was correlated with positive- and negative-strand RNA quantitative detection and the release of infectious particles. In addition, chloroquine treatment of FTOC and single-thymocyte suspensions suggested that MHC class I upregulation on thymocytes was the result of direct infection rather than caused by production of soluble factors such as alpha interferon. Thus, CVB4 E2 can infect human fetal thymocytes, which subsequently results in quantitative and qualitative abnormalities of these cells.

Indexed as

Cell DifferentiationCoxsackievirus InfectionsEnterovirus B, HumanFetusHistocompatibility Antigens Class IHumansInterferon-alphaLymphocyte CountOrgan Culture TechniquesThymus GlandT-LymphocytesVirus ReplicationHistocompatibility Antigens Class IInterferon-alpha

Identifiers

PMID15331720
PMCPMC514990
OpenAlexW2118372327

What OpenQuestion holds

Textmetadata
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.