Evidence map›Paper›PMID 20231413›Full record

ArticleInfection and immunity2010

Intrapulmonary administration of leukotriene B4 enhances pulmonary host defense against pneumococcal pneumonia.

Peter Mancuso, Casey Lewis, Carlos Henrique Serezani, Deepti Goel, Marc Peters-Golden

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
4.0field-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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Metabolites of prostaglandin synthases as potential biomarkers of Lyme disease severity and symptom resolution.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    Pooled it
  2. Article
  3. Leukotrienes in Innate Immunity: Still Underappreciated after All These Years?Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  4. Article
  5. Article
  6. Neutrophil Recruitment in Pneumococcal Pneumonia.Frontiers in cellular and infection microbiology · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Leukotriene BNature microbiology · 2019
    Article
  13. Article
  14. Article
  15. Too much of a good thing: How modulating LTBSeminars in immunology · 2017
    Review
  16. Review
  17. Macrophage LTBJournal of lipid research · 2017
    Article
  18. Article
  19. Article
  20. Obesity: impact of infections and response to vaccines.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2016
    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

5 authors at 1 institution in 1 country.

Peter MancusoDepartment of Environmental Health Sciences, School of Public Health, University of Michigan, SPHI A Tower, 109 S. Observatory St, Ann Arbor, MI 48109-2029, USA. pmancuso@umich.edu
Casey Lewis
Carlos Henrique Serezani
Deepti Goel
Marc Peters-Golden
Michigan Medicine · US

Funding

Regulation of Pulmonary Host Defense by LeptinR01HL077417 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MANCUSO, PETER · 2006 to 2010
$1.8M
NHLBI NIH HHS HL077417NHLBI NIH HHS R01 HL077417
6 · The paper itself

Abstract

Leukotriene B(4) (LTB(4)) is a potent lipid mediator of inflammation formed by the 5-lipoxygenase (5-LO)-catalyzed oxidation of arachidonic acid. We have previously shown that (i) LTB(4) is generated during infection, (ii) its biosynthesis is essential for optimal antimicrobial host defense, (iii) LT deficiency is associated with clinical states of immunocompromise, and (iv) exogenous LTB(4) augments antimicrobial functions in phagocytes. Here, we sought to determine whether the administration of LTB(4) has therapeutic potential in a mouse model of pneumonia. Wild-type and 5-LO knockout mice were challenged with Streptococcus pneumoniae via the intranasal route, and bacterial burdens, leukocyte counts, and cytokine levels were determined. LTB(4) was administered via the intraperitoneal, intravenous, and intranasal routes prior to pneumococcal infection and by aerosol 24 h following infection. Leukocytes recovered from mice given S. pneumoniae and treated with aerosolized LTB(4) were evaluated for expression levels of the p47phox subunit of NADPH oxidase. Intrapulmonary but not systemic pretreatment with LTB(4) significantly reduced the lung S. pneumoniae burden in wild-type mice. Aerosolized LTB(4) was effective at improving lung bacterial clearance when administered postinoculation in animals with established infection and exhibited greater potency in 5-LO knockout animals, which also exhibited greater baseline susceptibility. Augmented bacterial clearance in response to LTB(4) was associated with enhanced monocyte recruitment and leukocyte expression of p47phox. The results of the current study in an animal model serve as a proof of concept for the potential utility of treatment with aerosolized LTB(4) as an immunostimulatory strategy in patients with bacterial pneumonia.

Indexed as

Administration, InhalationAerosolsAnimalsArachidonate 5-LipoxygenaseBiological ProductsColony Count, MicrobialCytokinesImmunologic FactorsInjections, IntraperitonealInjections, IntravenousLeukocyte CountLeukotriene B4LungMiceMice, KnockoutPneumonia, PneumococcalAerosolsArachidonate 5-LipoxygenaseBiological ProductsCytokinesImmunologic FactorsLeukotriene B4

Identifiers

PMID20231413
PMCPMC2863513
OpenAlexW2113356134

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.