Evidence map›Paper›PMID 23949004›Full record

ReviewToxins2013

Bacterial toxins fuel disease progression in cutaneous T-cell lymphoma.

Andreas Willerslev-Olsen, Thorbjørn Krejsgaard, Lise M Lindahl, Charlotte Menne Bonefeld, Mariusz A Wasik, Sergei B Koralov, Carsten Geisler, Mogens Kilian, Lars Iversen, Anders Woetmann and 1 more

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in Toxins, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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.

NCT02836886 completednot on this mapstarted 2016, after this paper: background citation

Searching for Oncogenic Viruses in Sézary Cells Using a Novel Viral Discovery Technique, VirCapSeq-VERT

TypeobservationalSponsorColumbia UniversityRan2016 to 2016Enrolled6ConditionsLymphoma, T-Cell, Cutaneous, Sézary Syndrome
NCT07781449 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

An Investigator-Initiated, Descriptive, Proof-of-Concept, Open-Label Pilot Study Focusing on Topical JAK Inhibition as a Novel Treatment of Cutaneous T-Cell Lymphoma

TypeinterventionalSponsorAarhus University HospitalRan2026 to 2030Enrolled15ConditionsMycosis Fungoides, Cutaneous T-cell LymphomaArmsdelgocitinib
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Role of Antigenic Stimulation in Cutaneous T-Cell Lymphomas.The Journal of investigative dermatology · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. miRNA Signature in Early-stage Mycosis Fungoides.Acta dermato-venereologica · 2022
    Article
  19. Nasal Dysbiosis in Cutaneous T-Cell Lymphoma Is Characterized by Shifts in Relative Abundances of Non-JID innovations : skin science from molecules to population health · 2022
    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

11 authors at 5 institutions in 2 countries.

Andreas Willerslev-OlsenDepartment of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen 2200, Denmark.
Thorbjørn Krejsgaard
Lise M Lindahl
Charlotte Menne Bonefeld
Mariusz A Wasik
Sergei B Koralov
Carsten Geisler
Mogens Kilian
Lars Iversen
Anders Woetmann
Niels Odum
University of Copenhagen · DKAarhus University Hospital · DKAarhus University · DKNYU Langone Health · USUniversity of Pennsylvania · US

Funding

Jak/STAT signaling in human T-cell lymphomasR01CA089194 · NCI · UNIVERSITY OF PENNSYLVANIA · PI WASIK, MARIUSZ A. · 2001 to 2010
$2.5M
NCI NIH HHS CA89194NCI NIH HHS R01 CA089194
6 · The paper itself

Abstract

In patients with cutaneous T-cell lymphoma (CTCL) bacterial infections constitute a major clinical problem caused by compromised skin barrier and a progressive immunodeficiency. Indeed, the majority of patients with advanced disease die from infections with bacteria, e.g., Staphylococcus aureus. Bacterial toxins such as staphylococcal enterotoxins (SE) have long been suspected to be involved in the pathogenesis in CTCL. Here, we review links between bacterial infections and CTCL with focus on earlier studies addressing a direct role of SE on malignant T cells and recent data indicating novel indirect mechanisms involving SE- and cytokine-driven cross-talk between malignant- and non-malignant T cells.

Indexed as

Bacterial InfectionsBacterial ToxinsCytokinesDisease ProgressionDrug Resistance, BacterialEnterotoxinsGenes, T-Cell Receptor betaHumansLymphoma, T-Cell, CutaneousMorbidityPrevalenceSkin NeoplasmsStaphylococcus aureusT-LymphocytesBacterial ToxinsCytokinesEnterotoxins

Identifiers

PMID23949004
PMCPMC3760043
OpenAlexW1984523723

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.