Evidence map›Paper›PMID 12065522›Full record

ArticleInfection and immunity2002

In vivo effects of a synthetic 2-kilodalton macrophage-activating lipopeptide of Mycoplasma fermentans after pulmonary application.

Anke Lührmann, Ursula Deiters, Julia Skokowa, Michaela Hanke, Johannes E Gessner, Peter F Mühlradt, Reinhard Pabst, Thomas Tschernig

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Cellular Microbiology of Mycoplasma canis.Infection and immunity · 2016
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Nickel alterations of TLR2-dependent chemokine profiles in lung fibroblasts are mediated by COX-2.American journal of respiratory cell and molecular biology · 2008
    Article
  17. Contagious bovine pleuropneumonia: a rationale for the development of a mucosal sub-unit vaccine.Comparative immunology, microbiology and infectious diseases · 2008
    Review
  18. Modulation of asthma and allergy by addressing toll-like receptor 2.Journal of occupational medicine and toxicology (London, England) · 2008
    Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Anke LührmannDepartment of Functional and Applied Anatomy, Medical School of Hannover, 30623 Hannover, Germany. luehrmann.anke@mh.hannover.de
Ursula Deiters
Julia Skokowa
Michaela Hanke
Johannes E Gessner
Peter F Mühlradt
Reinhard Pabst
Thomas Tschernig
Helmholtz Centre for Infection Research · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycoplasmas can cause interstitial pneumonias inducing critical illness in humans and animals. Mycoplasma infections are characterized by an influx of neutrophils, followed by an accumulation of macrophages and lymphocytes. The present study deals with the question of which mycoplasmal components cause this host reaction. The mycoplasma-derived, macrophage-activating lipopeptide 2S-MALP-2 was used to mimic the sequelae of a mycoplasma infection. To this end, 2S-MALP-2 was intratracheally instilled into the lungs of Lewis rats, and the bronchoalveolar lavage cells were examined at different times after different doses of 2S-MALP-2. Application of 2.5 microg induced a pronounced leukocyte accumulation in the bronchoalveolar space. At 24 h after 2S-MALP-2 administration, the majority of leukocytes consisted of neutrophils, followed by macrophages, peaking on days 2 and 3. Lymphocyte numbers, although amounting to only a few percent of the total bronchoalveolar lavage cells, also increased significantly, with maximal lymphocyte accumulation occurring by 72 h after instillation. The leukocyte count of the lung interstitium was increased on day 3 after treatment. After 10 days all investigated cell populations returned to control levels. Transient chemotactic activity for neutrophils was detected in the bronchoalveolar lavage fluid early after 2S-MALP-2 application, followed by monocyte chemoattractant protein-1 activity (MCP-1) in lung homogenates. MCP-1 was produced by bronchoalveolar lavage cells upon stimulation with 2S-MALP-2. Our data indicate that mycoplasmal lipoproteins and lipopeptides are probably the most relevant mycoplasmal components for the early host reaction. The primary target cells are likely to be the alveolar macrophages liberating chemokines, which attract further leukocytes.

Indexed as

AnimalsBacterial ProteinsBronchoalveolar LavageCell CountChemokine CCL2Chemokine CCL5Chemotaxis, LeukocyteDose-Response Relationship, DrugInterleukin-16LeukocytesLipopeptidesLipoproteinsLungLymphocytesMacrophage ActivationMacrophages, AlveolarBacterial ProteinsChemokine CCL2Chemokine CCL5Interleukin-16LipopeptidesLipoproteinsmacrophage stimulatory lipopeptide 2Oligopeptides

Identifiers

PMID12065522
PMCPMC128036
OpenAlexW2169644036

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.