Evidence map›Paper›PMID 24688024›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Immunological priming requires regulatory T cells and IL-10-producing macrophages to accelerate resolution from severe lung inflammation.

Neil R Aggarwal, Kenji Tsushima, Yoshiki Eto, Ashutosh Tripathi, Pooja Mandke, Jason R Mock, Brian T Garibaldi, Benjamin D Singer, Venkataramana K Sidhaye, Maureen R Horton and 2 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. 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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. CNS1-dependent regulatory T cells shape recovery from acute lung injury.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  2. Article
  3. T Regulatory Mechanisms in Airway and Interstitial Lung Disease.Seminars in respiratory and critical care medicine · 2025
    Review
  4. Review
  5. Review
  6. The innate immune brakes of the lung.Frontiers in immunology · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Frontiers in pharmacology · 2020
    Article
  14. Immunometabolism of pro-repair cells.The Journal of clinical investigation · 2019
    Review
  15. Article
  16. Integrative Physiology of Pneumonia.Physiological reviews · 2018
    Review
  17. Article
  18. Article
  19. Report of the ISHLT Working Group on Primary Lung Graft Dysfunction Part III: Mechanisms: A 2016 Consensus Group Statement of the International Society for Heart and Lung Transplantation.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2017
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Neil R Aggarwal *Division of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Kenji Tsushima *Division of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Yoshiki EtoDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Ashutosh TripathiDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Pooja MandkeDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Jason R MockDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Brian T GaribaldiDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Benjamin D SingerDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Venkataramana K SidhayeDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Maureen R HortonDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Landon S KingDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Franco R D'AlessioDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224.
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

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
Modest supplemental oxygen worsens lung injury in a murine model of sepsisF32HL090200 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI AGGARWAL, NEIL RAJ · 2008 to 2008
$51k
NHLBI NIH HHS F32 HL090200NHLBI NIH HHS HL010342NHLBI NIH HHS HL089346NHLBI NIH HHS P01 HL010342NHLBI NIH HHS R00HL103793NHLBI NIH HHS R00 HL103973NHLBI NIH HHS R01 HL089346
6 · The paper itself

Abstract

Overwhelming lung inflammation frequently occurs following exposure to both direct infectious and noninfectious agents and is a leading cause of mortality worldwide. In that context, immunomodulatory strategies may be used to limit severity of impending organ damage. We sought to determine whether priming the lung by activating the immune system, or immunological priming, could accelerate resolution of severe lung inflammation. We assessed the importance of alveolar macrophages, regulatory T cells, and their potential interaction during immunological priming. We demonstrate that oropharyngeal delivery of low-dose LPS can immunologically prime the lung to augment alveolar macrophage production of IL-10 and enhance resolution of lung inflammation induced by a lethal dose of LPS or by Pseudomonas bacterial pneumonia. IL-10-deficient mice did not achieve priming and were unable to accelerate lung injury resolution. Depletion of lung macrophages or regulatory T cells during the priming response completely abrogated the positive effect of immunological priming on resolution of lung inflammation and significantly reduced alveolar macrophage IL-10 production. Finally, we demonstrated that oropharyngeal delivery of synthetic CpG-oligonucleotides elicited minimal lung inflammation compared with low-dose LPS but nonetheless primed the lung to accelerate resolution of lung injury following subsequent lethal LPS exposure. Immunological priming is a viable immunomodulatory strategy used to enhance resolution in an experimental acute lung injury model with the potential for therapeutic benefit against a wide array of injurious exposures.

Indexed as

AnimalsCytokinesFlow CytometryInterleukin-10LipopolysaccharidesMacrophages, AlveolarMaleMiceMice, Inbred C57BLMice, KnockoutPneumoniaT-Lymphocytes, RegulatoryVaccinationCytokinesIL10 protein, mouseInterleukin-10Lipopolysaccharides

Identifiers

PMID24688024
PMCPMC4001810
OpenAlexW2126698946

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.