Evidence map›Paper›PMID 28868524›Full record

ArticleImmunoHorizons2017

Divergent Specificity Development of IgG1 and IgG4 Autoantibodies in Endemic Pemphigus Foliaceus (Fogo Selvagem).

Mike Maldonado, Luis A Diaz, Phillip Prisayanh, Jinsheng Yang, Bahjat F Qaqish, Valeria Aoki, Gunter Hans-Filho, Evandro A Rivitti, Donna A Culton, Ye Qian

Open access · goldAbstract read
In one paragraph

Article in ImmunoHorizons, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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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

10 authors at 3 institutions in 2 countries.

Mike MaldonadoDepartment of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Luis A DiazDepartment of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Phillip PrisayanhDepartment of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Jinsheng YangDepartment of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Bahjat F QaqishDepartment of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Valeria AokiDepartment of Dermatology, University of Sao Paulo Medical School, Sao Paulo, CEP-05403-002, Brazil.
Gunter Hans-FilhoDepartamento de Dermatologia, Universidade Federal de Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, 79002212, Brazil.
Evandro A RivittiDepartment of Dermatology, University of Sao Paulo Medical School, Sao Paulo, CEP-05403-002, Brazil.
Donna A CultonDepartment of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Ye QianDepartment of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
University of North Carolina at Chapel Hill · USUniversidade de São Paulo · BRUniversidade 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
The IgE Antibody Response to Dsg1 and Environmental Antigens in Endemic Pemphigus FoliaceusR01AR067315 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI QIAN, YE · 2015 to 2019
$1.7M
NIAMS NIH HHS R01 AR032599NIAMS NIH HHS R01 AR067315
6 · The paper itself

Abstract

We have shown that although the IgG response in fogo selvagem (FS) is mainly restricted to desmoglein (Dsg) 1, other keratinocyte cadherins are also targeted by FS patients and healthy control subjects living in the endemic region of Limão Verde, Brazil (endemic controls). Evaluating nonpathogenic IgG1 and pathogenic IgG4 subclass responses to desmosomal proteins may reveal important differences between pathogenic and nonpathogenic responses, and how these differences relate to the pathogenic IgG4 response and resultant FS. In this study, we tested by ELISA >100 sera from each FS patient, endemic control, and nonendemic control for IgG1 and IgG4 autoantibodies to keratinocyte cadherins besides Dsg1. IgG1 and IgG4 subclass responses in endemic controls are highly correlated between Dsg1 and other keratinocyte cadherins. This correlation persists in the IgG1 response among FS patients, but diminishes in IgG4 response, suggesting that IgG1 binds highly conserved linear epitopes among cadherins, whereas IgG4 binds mainly specific conformational epitopes on Dsg1. A confirmatory test comparing serum samples of 11 individuals before and after their FS onset substantiated our findings that IgG1 recognizes primarily linear epitopes on Dsg1 both before and after disease onset, whereas IgG4 recognizes primarily linear epitopes before disease onset, but recognizes more conformational epitopes on Dsg1 after the onset of disease. This study may provide a mechanism by which a specificity convergence of the IgG4 response to unique Dsg1 epitopes, most likely conformational pathogenic epitopes, leads to the onset of FS disease.

Identifiers

PMID28868524
PMCPMC5577939
OpenAlexW2741433331

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Registered trials

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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.