Evidence map›Paper›PMID 10642599›Full record

ArticleThe Journal of clinical investigation2000

Desmoglein-1-specific T lymphocytes from patients with endemic pemphigus foliaceus (fogo selvagem).

M S Lin, C L Fu, V Aoki, G Hans-Filho, E A Rivitti, J R Moraes, M E Moraes, A M Lazaro, G J Giudice, P Stastny and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

19 citing papers in PubMed, 88 citations in OpenAlex.

  1. CD4Current molecular medicine · 2025
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  3. Review
  4. Review
  5. Article
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  7. Article
  8. Review
  9. Article
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  11. Endemic pemphigus over a century: Part II.North American journal of medical sciences · 2010
    Article
  12. Article
  13. T cell control in autoimmune bullous skin disorders.The Journal of clinical investigation · 2006
    Review
  14. Article
  15. High levels of interleukin-1 in patients with endemic pemphigus foliaceus.Clinical and diagnostic laboratory immunology · 2003
    Article
  16. Article
  17. Article
  18. Article
  19. 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

11 authors at 5 institutions in 2 countries.

M S LinDepartment of Dermatology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA. mslin@post.its.mcw.edu
C L Fu
V Aoki
G Hans-Filho
E A Rivitti
J R Moraes
M E Moraes
A M Lazaro
G J Giudice
P Stastny
L A Diaz
Medical College of Wisconsin · USMilitary Institute of Engineering · BRUniversidade de São Paulo · BRSouthwestern Medical CenterUniversidade Federal de Mato Grosso do Sul · BR

Funding

ETIOLOGY AND PATHOGENESIS OF PEMPHIGUSR01AR032599 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DIAZ, LUIS A. · 1987 to 2017
$5.2M
PEMPHIGUS AND PEMPHIGOIDR01AR032081 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DIAZ, LUIS A. · 1986 to 2011
$3.3M
HEMIDESMOSOMES IN BULLOUS PEMPHIGOIDR01AR040410 · NIAMS · UNIVERSITY OF IOWA · PI GIUDICE, GEORGE J · 1995 to 2007
$1.8M
POLYMORPHIC SEQUENCES OF HLA ALLELESR01HL047145 · NHLBI · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI STASTNY, PETER · 1991 to 1994
–
THE ROLE OF COMPLEMENT RECEPTOR 2 IN THE IMMUNE RESPONSEU01AI034621 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MUNFORD, ROBERT S · 1993 to 1996
–
NHLBI NIH HHS R01-HL47145NIAID NIH HHS UO1-AI34621NIAMS NIH HHS R01 AR032081NIAMS NIH HHS R01 AR032599NIAMS NIH HHS R01 AR040410NIAMS NIH HHS R01-AR40410
6 · The paper itself

Abstract

Fogo selvagem (FS), the endemic form of pemphigus foliaceus, is a cutaneous autoimmune disease characterized by subcorneal blistering of the epidermis and the production of autoantibodies against the desmosomal antigen desmoglein-1 (Dsg1). Previously, we showed that mice injected with autoantibodies from FS patients develop a skin disease that reproduces the clinical, histological, and immunological features of FS, indicating that autoantibodies play an essential role in the development of this disease. The purpose of this study was to characterize the autoimmune T-cell response associated with FS. We provide here the first evidence, to our knowledge, that the great majority of FS patients have circulating T lymphocytes that specifically proliferate in response to the extracellular domain of Dsg1. Long-term T cells developed from these patients also responded to Dsg1, and this antigen-specific response was shown to be restricted to HLA-DR molecules. These Dsg1-reactive FS T cells exhibited a CD4-positive memory T-cell phenotype and produced a T helper 2-like cytokine profile. These findings represent the initial steps in defining the role of T cells in FS autoimmunity.

Indexed as

AdolescentAdultAgedAntigens, CDAutoantigensCadherinsClone CellsCytokinesDesmoglein 1EpitopesFemaleFlow CytometryGenes, MHC Class IIHistocompatibility TestingHumansImmunophenotypingAntigens, CDAutoantigensCadherinsCytokinesDesmoglein 1EpitopesReceptors, Antigen, T-Cell, alpha-betaRecombinant Fusion Proteins

Identifiers

PMID10642599
PMCPMC377431
OpenAlexW2020311023

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.