Evidence map›Paper›PMID 17322386›Full record

ArticleThe American journal of pathology2007

Role of granulocyte macrophage colony-stimulating factor in host defense against pulmonary Cryptococcus neoformans infection during murine allergic bronchopulmonary mycosis.

Gwo-Hsiao Chen, Michal A Olszewski, Roderick A McDonald, Jason C Wells, Robert Paine, Gary B Huffnagle, Galen B Toews

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

50 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Article
  3. Frontiers in medicine · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Role of GM-CSF in lung balance and disease.Frontiers in immunology · 2023
    Review
  8. GM-CSFCell reports · 2022
    Article
  9. Article
  10. Article
  11. Proteomics ofInternational journal of molecular sciences · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Autoantibody-Mediated Pulmonary Alveolar Proteinosis in Rasgrp1-Deficient Mice.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
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

7 authors at 2 institutions in 3 countries.

Gwo-Hsiao ChenDivision of Pulmonary and Critical Care Medicine, University of Michigan Medical School, Ann Arbor, MI 48109-0642, USA. gchen@umich.edu
Michal A Olszewski
Roderick A McDonald
Jason C Wells
Robert Paine
Gary B Huffnagle
Galen B Toews
University of Michigan–Ann Arbor · USBipar · FR

Funding

MACROPHAGE RECRUITMENT/ACTIVATION IN LUNG DEFENSER01HL051082 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TOEWS, GALEN B · 1994 to 2007
$2.5M
Role of Fungal Microflora in Mucosal Tolerance/ImmunityR01AI064479 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUFFNAGLE, GARY B · 2005 to 2009
$1.8M
Role of Oxylipins in Cryptococcal PathogenesisR01AI059201 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUFFNAGLE, GARY B · 2004 to 2008
$1.7M
RESPIRATORY FAILURE IN A MODEL OF P. CARINII PNEUMONIAR01HL064558 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PAINE, ROBERT · 2000 to 2004
$1.4M
NHLBI NIH HHS R01 HL051082NHLBI NIH HHS R01 HL064558NIAID NIH HHS R01 AI059201NIAID NIH HHS R01 AI064479
6 · The paper itself

Abstract

We investigated the role of granulocyte macrophage colony-stimulating factor (GM-CSF) in host defense in a murine model of pulmonary cryptococcosis induced by intratracheal inoculation of Cryptococcus neoformans. Pulmonary C. neoformans infection of C57BL/6 mice is an established model of an allergic bronchopulmonary mycosis. Our objective was to determine whether GM-CSF regulates the pulmonary Th2 immune response in C. neoformans-infected C57BL/6 mice. Long-term pulmonary fungistasis was lost in GM-CSF knockout (GM(-/-)) mice, resulting in increased pulmonary burden of fungi between weeks 3 and 5. GM-CSF was required for the early influx of macrophages and CD4 and CD8 T cells into the lungs but was not required later in the infection. Lack of GM-CSF also resulted in reduced eosinophil recruitment and delayed recruitment of mononuclear cells into the airspace. Macrophages from GM(+/+) mice showed numerous hallmarks of alternatively activated macrophages: higher numbers of intracellular cryptococci, YM1 crystals, and induction of CCL17. These hallmarks are absent in macrophages from GM(-/-) mice. Mucus-producing goblet cells were abundantly present within the bronchial epithelial layer in GM(+/+) mice but not in GM(-/-) mice at week 5 after infection. Production of both Th1 and Th2 cytokines was impaired in the absence of GM-CSF, consistent with both reduced C. neoformans clearance and absence of allergic lung pathology.

Indexed as

AnimalsBronchoalveolar Lavage FluidCryptococcosisCryptococcus neoformansFlow CytometryGranulocyte-Macrophage Colony-Stimulating FactorLung Diseases, FungalMacrophagesMiceMice, Inbred C57BLMice, KnockoutRespiratory HypersensitivityTh2 CellsGranulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID17322386
PMCPMC1864884
OpenAlexW2010320716

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.