Evidence map›Paper›PMID 23791647›Full record

ArticleImmunity2013

Pathogen-specific Treg cells expand early during mycobacterium tuberculosis infection but are later eliminated in response to Interleukin-12.

Shahin Shafiani, Crystal Dinh, James M Ertelt, Albanus O Moguche, Imran Siddiqui, Kate S Smigiel, Pawan Sharma, Daniel J Campbell, Sing Sing Way, Kevin B Urdahl

Abstract read
In one paragraph

Article in Immunity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
9.3field-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

89 citing papers in PubMed, 144 citations in OpenAlex.

  1. Article
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  5. Immune dysregulation inFrontiers in immunology · 2026
    Review
  6. Article
  7. Article
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  9. Article
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  15. TOLLIP Optimizes Dendritic Cell Maturation to Lipopolysaccharide andJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review

29 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

Shahin ShafianiSeattle Biomedical Research Institute, Seattle, WA 98109, USA.
Crystal Dinh
James M Ertelt
Albanus O Moguche
Imran Siddiqui
Kate S Smigiel
Pawan Sharma
Daniel J Campbell
Sing Sing Way
Kevin B Urdahl
Center for Infectious Disease Research · USCincinnati Children's Hospital Medical Center · USUniversity of Washington · USInternational Centre for Genetic Engineering and Biotechnology · IN

Funding

T regulatory cells and immunity in tuberculosisR01AI076327 · NIAID · UNIVERSITY OF WASHINGTON · PI URDAHL, KEVIN B · 2009 to 2018
$4.5M
The Immune Pathogenesis of Prenatal Listeria monocytogenes InfectionR01AI100934 · NIAID · UNIVERSITY OF MINNESOTA · PI WAY, SING SING · 2012 to 2016
$2.3M
Functional specialization of Foxp3+ regulatory T cellsR01AI085130 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J · 2010 to 2014
$2.1M
Regulatory T cells dictate immunity during persistent Salmonella infectionR01AI087830 · NIAID · UNIVERSITY OF MINNESOTA · PI WAY, SING SING · 2010 to 2014
$1.8M
Research Training on Intracellular Pathogens including Plasmodium, Leishmania andD43TW000924 · FIC · UNIVERSITY OF WASHINGTON · PI STUART, KENNETH D · 1997 to 2010
$1.2M
FIC NIH HHS D43 TW000924FIC NIH HHS D43TW000924NIAID NIH HHS R01 AI076327NIAID NIH HHS R01AI076327NIAID NIH HHS R01 AI085130NIAID NIH HHS R01AI085130NIAID NIH HHS R01 AI087830NIAID NIH HHS R01AI087830NIAID NIH HHS R01 AI100934NIAID NIH HHS R01AI100934
6 · The paper itself

Abstract

Thymically derived Foxp3⁺ regulatory T (Treg) cells have a propensity to recognize self-peptide:MHC complexes, but their ability to respond to epitope-defined foreign antigens during infectious challenge has not been demonstrated. Here we show that pulmonary infection with Mycobacterium tuberculosis (Mtb), but not Listeria monocytogenes (Lm), induced robust lymph node expansion of a highly activated population of pathogen-specific Treg cells from the pre-existing pool of thymically derived Treg cells. These antigen-specific Treg cells peaked in numbers 3 weeks after infection but subsequently underwent selective elimination driven, in part, by interleukin-12-induced intrinsic expression of the Th1-cell-promoting transcription factor T-bet. Thus, the initial Mtb-induced inflammatory response promotes pathogen-specific Treg cell proliferation, but these cells are actively culled later, probably to prevent suppression during later stages of infection. These findings have important implications for the prevention and treatment of tuberculosis and other chronic diseases in which antigen-specific Treg cells restrict immunity.

Indexed as

AnimalsAntigens, BacterialBacterial ProteinsCell ProliferationCells, CulturedClonal DeletionEpitopes, T-LymphocyteForkhead Transcription FactorsImmune EvasionInterleukin-12Lymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMycobacterium tuberculosisPeptide FragmentsAntigens, BacterialBacterial ProteinsEpitopes, T-LymphocyteESAT-6 protein, Mycobacterium tuberculosisForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-12Peptide FragmentsT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID23791647
PMCPMC3827956
OpenAlexW2061722689

What OpenQuestion holds

Textmetadata
LicenceTDM
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.