Evidence map›Paper›PMID 17709423›Full record

ArticleThe Journal of experimental medicine2007

Expansion and function of Foxp3-expressing T regulatory cells during tuberculosis.

James P Scott-Browne, Shahin Shafiani, Glady's Tucker-Heard, Kumiko Ishida-Tsubota, Jason D Fontenot, Alexander Y Rudensky, Michael J Bevan, Kevin B Urdahl

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 200 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
200citing papers in PubMed, 1 pooled it
12.5field-weighted citation impact, top 1% 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

200 citing papers in PubMed, 1 synthesis or guideline pooled it, 391 citations in OpenAlex.

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  20. The dark side of Tregs during aging.Frontiers in immunology · 2022
    Review

140 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

8 authors at 2 institutions in 1 country.

James P Scott-BrowneDepartment of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Shahin Shafiani
Glady's Tucker-Heard
Kumiko Ishida-Tsubota
Jason D Fontenot
Alexander Y Rudensky
Michael J Bevan
Kevin B Urdahl
Pediatrics and Genetics · USUniversity of Washington · US

Funding

CYTOTOXIC RESPONSE TO HISTOCOMPATIBILITY ANTIGENSR01AI019335 · NIAID · UNIVERSITY OF WASHINGTON · PI BEVAN, MICHAEL J · 1985 to 2012
$4.4M
MHC class 1 molecules in immunity against tuberculosisK08AI055889 · NIAID · UNIVERSITY OF WASHINGTON · PI URDAHL, KEVIN B · 2003 to 2005
$362k
CYTOTOXIC RESPONSE TO HISTOCOMPATIBILITY ANTIGENSR37AI019335 · NIAID · UNIVERSITY OF WASHINGTON · PI BEVAN, MICHAEL J · 1988 to 1997
–
NIAID NIH HHS AI 055889-01NIAID NIH HHS AI 19335NIAID NIH HHS K08 AI055889NIAID NIH HHS R01 AI019335Wellcome Trust
6 · The paper itself

Abstract

Mycobacterium tuberculosis (Mtb) frequently establishes persistent infections that may be facilitated by mechanisms that dampen immunity. T regulatory (T reg) cells, a subset of CD4(+) T cells that are essential for preventing autoimmunity, can also suppress antimicrobial immune responses. We use Foxp3-GFP mice to track the activity of T reg cells after aerosol infection with Mtb. We report that during tuberculosis, T reg cells proliferate in the pulmonary lymph nodes (pLNs), change their cell surface phenotype, and accumulate in the pLNs and lung at a rate parallel to the accumulation of effector T cells. In the Mtb-infected lung, T reg cells accumulate in high numbers in all sites where CD4(+) T cells are found, including perivascular/peribronchiolar regions and within lymphoid aggregates of granulomas. To determine the role of T reg cells in the immune response to tuberculosis, we generated mixed bone marrow chimeric mice in which all cells capable of expressing Foxp3 expressed Thy1.1. When T reg cells were depleted by administration of anti-Thy1.1 before aerosol infection with Mtb, we observed approximately 1 log less of colony-forming units of Mtb in the lungs. Thus, after aerosol infection, T reg cells proliferate and accumulate at sites of infection, and have the capacity to suppress immune responses that contribute to the control of Mtb.

Indexed as

AnimalsBiomarkersBone Marrow CellsCell MovementCell ProliferationChimeraColony Count, MicrobialForkhead Transcription FactorsGranulomaInterleukin-10LungLymph NodesMiceMice, Inbred C57BLMycobacterium tuberculosisPhenotypeBiomarkersForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-10

Identifiers

PMID17709423
PMCPMC2118702
OpenAlexW2097509788

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.