Evidence map›Paper›PMID 19448155›Full record

ArticleAmerican journal of respiratory cell and molecular biology2010

Flt3-L increases CD4+CD25+Foxp3+ICOS+ cells in the lungs of cockroach-sensitized and -challenged mice.

Halvor S McGee, Jehad H Edwan, Devendra K Agrawal

Abstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. ICOSFrontiers in immunology · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Key mediators in the immunopathogenesis of allergic asthma.International immunopharmacology · 2014
    Review
  9. Article
  10. Clinical view on the importance of dendritic cells in asthma.Expert review of clinical immunology · 2013
    Review
  11. Review
  12. Article
  13. Article
  14. Pathogenesis of allergic airway inflammation.Current allergy and asthma reports · 2010
    Review
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

3 authors at 1 institution in 2 countries.

Halvor S McGeeDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, NE 68178, USA.
Jehad H Edwan
Devendra K Agrawal
Creighton University · US

Funding

FLT3-LIGAND, IMMUNOMODULATION AND THERAPY IN ASTHMAR01HL070885 · NHLBI · CREIGHTON UNIVERSITY · PI AGRAWAL, DEVENDRA K. · 2004 to 2008
$1.1M
NHLBI NIH HHS R01HL070885
6 · The paper itself

Abstract

We previously reported in an ovalbumin-induced model of allergic asthma that Fms-like tyrosine kinase 3 ligand (Flt3-L) reversed airway hyperresponsiveness (AHR) and airway inflammation, and increased the number of regulatory CD11c(high)CD8 alpha(high)CD11b(low) dendritic cells in the lung. In this study, we investigated the effect of Flt3-L in a clinically relevant aeroallergen-induced asthma on the phenotypic expression of lung T cells. Balb/c mice were sensitized and challenged with cockroach antigen (CRA), and AHR to methacholine was established. These mice received three intraperitoneal injections of anti-CD25 antibody (PC61; 250 microg) and Flt3-L (3 microg) daily for 10 days. Cytokines and Ig levels in the serum were measured and differential bronchoalveolar lavage fluid (BALF) cell counts were examined. Flt3-L reversed AHR to methacholine to the control level. Flt3-L significantly decreased levels of BALF IL-5, IFN-gamma, eosinophilia and substantially increased IL-10 and the number of CD4(+)CD25(+) Forkhead winged helix transcription factor box P3 (Foxp3(+)) IL-10(+) T cells in the lung. Administration of PC61 antibody blocked the effect of Flt3-L and substantially increased AHR, eosinophilia, and BALF IL-5 and IFN-gamma levels, and decreased BALF IL-10 levels and the number of CD4(+)CD25(+)Foxp3(+)IL-10(+) T cells. Flt3-L significantly decreased CD62-L, but increased inducible costimulatory molecule and Foxp3 mRNA expression in the CD4(+)CD25(+) T cells isolated from lungs of Flt3-L-treated, CRA-sensitized mice compared to CRA-sensitized mice without Flt3-L treatment and PBS control group. Flt3-L significantly inhibited the effect of CRA sensitization and challenge to increase GATA3 expression in lung CD4(+)CD25(+) T cells. Collectively, these data suggest that the therapeutic effect of Flt3-L is mediated by increased density of naturally occurring CD4(+)CD25(+)Foxp3(+)IL-10(+)ICOS(+) T-regulatory cells in the lung. Flt3-L could be a therapeutic strategy for the management and prevention of allergic asthma.

Indexed as

AnimalsAntibodiesAntigens, Differentiation, T-LymphocyteBronchial HyperreactivityCD4 AntigensCell CountCell SeparationCockroachesFlow CytometryForkhead Transcription FactorsGATA3 Transcription FactorGene Expression RegulationImmunizationInducible T-Cell Co-Stimulator ProteinInterleukin-2 Receptor alpha SubunitL-SelectinAntibodiesAntigens, Differentiation, T-LymphocyteCD4 Antigensflt3 ligand proteinForkhead Transcription FactorsFoxp3 protein, mouseGATA3 Transcription FactorIcos protein, mouseInducible T-Cell Co-Stimulator ProteinInterleukin-2 Receptor alpha SubunitL-SelectinMembrane ProteinsMethacholine ChlorideRNA, Messenger

Identifiers

PMID19448155
PMCPMC2830405
OpenAlexW2060698821

What OpenQuestion holds

Textmetadata
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.