Evidence map›Paper›PMID 23073617›Full record

ArticleJournal of clinical immunology2013

Sarcoidosis Th17 cells are ESAT-6 antigen specific but demonstrate reduced IFN-γ expression.

Bradley W Richmond, Kristen Ploetze, Joan Isom, Isfahan Chambers-Harris, Nicole A Braun, Thyneice Taylor, Susamma Abraham, Yolanda Mageto, Dan A Culver, Kyra A Oswald-Richter and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Overview of multi-omics approaches for pulmonary sarcoidosis.EC pulmonology and respiratory medicine · 2025
    Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Interleukin-17A plays a key role in pulmonary fibrosis followingExperimental biology and medicine (Maywood, N.J.) · 2023
    Article
  9. Article
  10. Article
  11. Immune mechanisms in fibrotic pulmonary sarcoidosis.European respiratory review : an official journal of the European Respiratory Society · 2022
    Review
  12. Article
  13. Article
  14. The Role of Oxidative Stress in Sarcoidosis.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. IL-17A Can PromoteFrontiers in immunology · 2019
    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 4 institutions in 1 country.

Bradley W RichmondDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical School, Nashville, TN 37232-2363, USA. Bradley.Richmond@vanderbilt.edu
Kristen Ploetze
Joan Isom
Isfahan Chambers-Harris
Nicole A Braun
Thyneice Taylor
Susamma Abraham
Yolanda Mageto
Dan A Culver
Kyra A Oswald-Richter
Wonder P Drake
Vanderbilt University · USCleveland Clinic · USUniversity of Vermont · USVanderbilt University Medical Center · US

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
YOHIMBINE AS A MODEL OF ORTHOSTATIC INTOLERANCEM01RR000095 · NCRR · VANDERBILT UNIVERSITY · PI DRAKE, WONDER P. · 1985 to 2008
$38.3M
Immunobiology of Blood and Vascular Systems Training ProgramT32HL069765 · NHLBI · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2002 to 2016
$6.5M
Interdisciplinary Training Program in Lung ResearchT32HL094296 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ray Stokes Peebles · 2008 to 2026
$6.3M
Investigation of the role of bacteria in the sarcoidosis trimolecular complexR01HL083839 · NHLBI · VANDERBILT UNIVERSITY · PI DRAKE, WONDER P. · 2006 to 2009
$1.5M
The Role of CD8 T Cells in Chronic Granulomatous InflammationK01HL103179 · NHLBI · VANDERBILT UNIVERSITY · PI OSWALD-RICHTER, KYRA A. · 2010 to 2014
$561k
Investigation of microbial hetergeneity to sarcoidosis and AAT clinical outcomeU01HL112694 · NHLBI · VANDERBILT UNIVERSITY · PI DRAKE, WONDER P. · 2012 to 2014
$463k
Summer Research Training Program in Heart, Lung and Vascular BiologyT35HL090555 · NHLBI · VANDERBILT UNIVERSITY · PI SWIFT, LARRY L. · 2008 to 2012
$369k
NCRR NIH HHS 1 UL1 RR024975NCRR NIH HHS M01 RR000095NCRR NIH HHS MO1 RR-00095NCRR NIH HHS UL1 RR024975NHLBI NIH HHS 1 U01HL112694-01NHLBI NIH HHS K01 HL103179NHLBI NIH HHS K01HL103179-01NHLBI NIH HHS R01 HL083839NHLBI NIH HHS R01-HL83839NHLBI NIH HHS T32 HL069765NHLBI NIH HHS T32HL069765-08NHLBI NIH HHS T32 HL094296NHLBI NIH HHS T32HL094296NHLBI NIH HHS T35 HL090555NHLBI NIH HHS T35HL090555NHLBI NIH HHS U01 HL112694
6 · The paper itself

Abstract

rationaleSarcoidosis is a granulomatous disease of unknown etiology. Many patients with sarcoidosis demonstrate antigen-specific immunity to mycobacterial virulence factors. Th-17 cells are crucial to the immune response in granulomatous inflammation, and have recently been shown to be present in greater numbers in the peripheral blood and bronchoalveolar lavage (BAL) fluid (BALF) of sarcoidosis patients than healthy controls. It is unclear whether Th-17 cells in sarcoidosis are specific for mycobacterial antigens, or whether they have similar functionality to control Th-17 cells.

methodsFlow cytometry was used to determine the numbers of Th-17 cells present in the peripheral blood and BALF of patients with sarcoidosis, the percentage of Th-17 cells that were specific to the mycobacterial virulence factor ESAT-6, and as well as to assess IFN-γ expression in Th-17 cells following polyclonal stimulation.

resultsPatients with sarcoidosis had greater numbers of Th-17 cells in the peripheral blood and BALF than controls and produced significantly more extracellular IL-17A (p = 0.03 and p = 0.02, respectively). ESAT-6 specific Th-17 cells were present in both peripheral blood and BALF of sarcoidosis patients (p < 0.001 and p = 0.03, respectively). After polyclonal stimulation, Th-17 cells from sarcoidosis patients produced less IFN-γ than healthy controls.

conclusionsPatients with sarcoidosis have mycobacterial antigen-specific Th-17 cells peripherally and in sites of active sarcoidosis involvement. Despite the Th1 immunophenotype of sarcoidosis immunology, the Th-17 cells have reduced IFN-γ expression, compared to healthy controls. This reduction in immunity may contribute to sarcoidosis pathogenesis.

Indexed as

AdultAntigens, BacterialBronchoalveolar Lavage FluidCase-Control StudiesFemaleHumansImmunophenotypingInterferon-gammaInterleukin-17MaleMiddle AgedReceptors, Antigen, T-Cell, gamma-deltaSarcoidosisTh17 CellsTh1 CellsAntigens, BacterialESAT-6 antigen, Mycobacterium lepraeInterferon-gammaInterleukin-17Receptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID23073617
PMCPMC3850764
OpenAlexW2078354108

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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.