Evidence map›Paper›PMID 24850425›Full record

ArticleMucosal immunology2014

Foxp3+ regulatory T cells promote lung epithelial proliferation.

J R Mock, B T Garibaldi, N R Aggarwal, J Jenkins, N Limjunyawong, B D Singer, E Chau, R Rabold, D C Files, V Sidhaye and 4 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04482621 (Decitabine for COVID-19 Pneumonia-ARDS Treatment), which is not on this map. Cited by 109 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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.

NCT04482621 phase2suspendednot on this mapstarted 2020, after this paper: background citation

Decitabine for COVID-19 Pneumonia-ARDS Treatment: DART Trial

TypeinterventionalSponsorJohns Hopkins UniversityRan2020 to 2026Enrolled33ConditionsCOVID-19ArmsDecitabine, Placebo Saline
3 · Its place in the literature

Who cites it

109 citing papers in PubMed, 1 synthesis or guideline pooled it, 147 citations in OpenAlex.

  1. Pooled it
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  4. CNS1-dependent regulatory T cells shape recovery from acute lung injury.Journal of immunology (Baltimore, Md. : 1950) · 2026
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49 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

14 authors at 3 institutions in 1 country.

J R MockDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
B T GaribaldiDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
N R AggarwalDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J JenkinsDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
N LimjunyawongDepartment of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
B D SingerDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
E ChauDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
R RaboldDepartment of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
D C FilesDivision of Pulmonary, Critical Care, Allergy, and Immunology, Department of Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
V SidhayeDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
W MitznerDepartment of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
E M WagnerDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
L S KingDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
F R D'AlessioDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins Medicine · USJohns Hopkins University · USWake Forest University · US

Funding

MULTIDISCIPLINARY TRAINING PROGRAM IN LUNG DISEASEST32HL007534 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Nadia N Hansel, Larissa A. Shimoda · 1985 to 2026
$28.3M
THE INTEGRATED FUNCTION OF RESPIRATION &CIRCULATIONP01HL010342 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MITZNER, WAYNE · 1985 to 2015
$24.4M
Phenotype-Specific Immune Responses in the Systemic VasculitidesP30AR053503 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI ROSEN, ANTONY · 2006 to 2015
$6.4M
Determinants of Resolution in Acute Lung InjuryR01HL089346 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KING, LANDON S · 2008 to 2012
$2.0M
Resolution and repair of acute lung injury by macrophage-derived iNOSR00HL103973 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI D'ALESSIO, FRANCO RAFAEL · 2012 to 2014
$713k
Stopping the Start: Understanding PanIN Initiation and ProgressionF32CA157044 · NCI · JOHNS HOPKINS UNIVERSITY · PI LUNDBERG, JENNIFER BAILEY · 2011 to 2011
$51k
Regulatory T Cell Modulation of the Alveolar Epithelium in Acute Lung InjuryF32HL110561 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MOCK, JASON ROBERT · 2012 to 2012
$51k
NCI NIH HHS F32 CA157044NHLBI NIH HHS F32 HL110561NHLBI NIH HHS F32HL110561NHLBI NIH HHS P01 HL010342NHLBI NIH HHS R00 HL103973NHLBI NIH HHS R00HL103973NHLBI NIH HHS R01 HL089346NHLBI NIH HHS R01HL089346NHLBI NIH HHS T32 HL007534NIAMS NIH HHS P30 AR053503
6 · The paper itself

Abstract

Acute respiratory distress syndrome (ARDS) causes significant morbidity and mortality each year. There is a paucity of information regarding the mechanisms necessary for ARDS resolution. Foxp3(+) regulatory T cells (Foxp3(+) T(reg) cells) have been shown to be an important determinant of resolution in an experimental model of lung injury. We demonstrate that intratracheal delivery of endotoxin (lipopolysaccharide) elicits alveolar epithelial damage from which the epithelium undergoes proliferation and repair. Epithelial proliferation coincided with an increase in Foxp3(+) T(reg) cells in the lung during the course of resolution. To dissect the role that Foxp3(+) T(reg) cells exert on epithelial proliferation, we depleted Foxp3(+) T(reg) cells, which led to decreased alveolar epithelial proliferation and delayed lung injury recovery. Furthermore, antibody-mediated blockade of CD103, an integrin, which binds to epithelial expressed E-cadherin decreased Foxp3(+) T(reg) numbers and decreased rates of epithelial proliferation after injury. In a non-inflammatory model of regenerative alveologenesis, left lung pneumonectomy, we found that Foxp3(+) T(reg) cells enhanced epithelial proliferation. Moreover, Foxp3(+) T(reg) cells co-cultured with primary type II alveolar cells (AT2) directly increased AT2 cell proliferation in a CD103-dependent manner. These studies provide evidence of a new and integral role for Foxp3(+) T(reg) cells in repair of the lung epithelium.

Indexed as

Cell ProliferationAlveolar Epithelial CellsAnimalsAntigens, CDForkhead Transcription FactorsIntegrin alpha ChainsLipopolysaccharidesMiceMice, KnockoutRespiratory Distress SyndromeRespiratory MucosaT-Lymphocytes, Regulatoryalpha E integrinsAntigens, CDForkhead Transcription FactorsFoxp3 protein, mouseIntegrin alpha ChainsLipopolysaccharides

Identifiers

PMID24850425
PMCPMC4205163
OpenAlexW2086194617

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.