Evidence map›Paper›PMID 15753209›Full record

ArticleThe Journal of experimental medicine2005

Mycobacterial catalase-peroxidase is a tissue antigen and target of the adaptive immune response in systemic sarcoidosis.

Zhimin Song, Lisa Marzilli, Brian M Greenlee, Edward S Chen, Richard F Silver, Frederic B Askin, Alvin S Teirstein, Ying Zhang, Robert J Cotter, David R Moller

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 139 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed, 3 pooled it
8.2field-weighted citation impact, top 2% 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

139 citing papers in PubMed, 3 syntheses or guidelines pooled it, 369 citations in OpenAlex.

  1. Sarcoidosis as an Autoimmune Disease.Frontiers in immunology · 2019
    Pooled it
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  4. Trial
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  11. The Renin-Angiotensin-Aldosterone System Regulates Sarcoidosis Granulomatous Inflammation.American journal of respiratory and critical care medicine · 2024
    Article
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  13. Article
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  15. Article
  16. Article
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79 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Zhimin SongDivision of Pulmonary and Critical Care Medicine, Department of Medicine, The Johns Hopkins University Bloomberg School of Public Health, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Lisa Marzilli
Brian M Greenlee
Edward S Chen
Richard F Silver
Frederic B Askin
Alvin S Teirstein
Ying Zhang
Robert J Cotter
David R Moller
Johns Hopkins University · USPulmonary and Critical Care Associates · USCase Western Reserve University · USMount Sinai Medical Center · US

Funding

Etiologic Antigens in SarcoidosisR01HL068019 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MOLLER, DAVID R · 2002 to 2006
$2.0M
REGULATION OF THL RESPONSES IN PULMONARY SARCOIDOSISR01HL054658 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MOLLER, DAVID R · 1996 to 2000
$221k
SEQUENCING OF CLASS I MHC PEPTIDES BY MASS SPECTROMETRYR01GM054882 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COTTER, ROBERT J. · 1996 to 1999
–
NHLBI NIH HHS HL-54658NHLBI NIH HHS HL-68019NHLBI NIH HHS R01 HL068019NIGMS NIH HHS GM-54882
6 · The paper itself

Abstract

Sarcoidosis is a disease of unknown etiology characterized by noncaseating epithelioid granulomas, oligoclonal CD4(+) T cell infiltrates, and immune complex formation. To identify pathogenic antigens relevant to immune-mediated granulomatous inflammation in sarcoidosis, we used a limited proteomics approach to detect tissue antigens that were poorly soluble in neutral detergent and resistant to protease digestion, consistent with the known biochemical properties of granuloma-inducing sarcoidosis tissue extracts. Tissue antigens with these characteristics were detected with immunoglobulin (Ig)G or F(ab')(2) fragments from the sera of sarcoidosis patients in 9 of 12 (75%) sarcoidosis tissues (150-160, 80, or 60-64 kD) but only 3 of 22 (14%) control tissues (all 62-64 kD; P = 0.0006). Matrix-assisted laser desorption/ionization time of flight mass spectrometry identified Mycobacterium tuberculosis catalase-peroxidase (mKatG) as one of these tissue antigens. Protein immunoblotting using anti-mKatG monoclonal antibodies independently confirmed the presence of mKatG in 5 of 9 (55%) sarcoidosis tissues but in none of 14 control tissues (P = 0.0037). IgG antibodies to recombinant mKatG were detected in the sera of 12 of 25 (48%) sarcoidosis patients compared with 0 of 11 (0%) purified protein derivative (PPD)(-) (P = 0.0059) and 4 of 10 (40%) PPD(+) (P = 0.7233) control subjects, suggesting that remnant mycobacterial catalase-peroxidase is one target of the adaptive immune response driving granulomatous inflammation in sarcoidosis.

Indexed as

Antigens, BacterialBacterial ProteinsBiopsyBlotting, WesternCatalaseDetergentsDNAHumansIn Situ HybridizationMycobacterium tuberculosisRecombinant ProteinsRNA, Ribosomal, 16SSarcoidosisSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAntigens, BacterialBacterial ProteinsCatalaseDetergentsDNAkatG protein, Mycobacterium tuberculosisRecombinant ProteinsRNA, Ribosomal, 16S

Identifiers

PMID15753209
PMCPMC2212832
OpenAlexW1977316020

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.