Evidence map›Paper›PMID 26248370›Full record

ArticleAntimicrobial agents and chemotherapy2015

Role of Interleukin-12 in Protection against Pulmonary Infection with Methicillin-Resistant Staphylococcus aureus.

Quang-Tam Nguyen, Yoichi Furuya, Sean Roberts, Dennis W Metzger

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Co-exposure to lipopolysaccharide and desert dust causes exacerbation of ovalbumin-induced allergic lung inflammation in mice via TLR4/MyD88-dependent and -independent pathways.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Transcriptomic Analysis on Responses of Murine Lungs toFrontiers in cellular and infection microbiology · 2017
    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

4 authors at 1 institution in 1 country.

Quang-Tam NguyenCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York, USA.
Yoichi FuruyaCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York, USA.
Sean RobertsCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York, USA.
Dennis W MetzgerCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York, USA metzged@mail.amc.edu.
Albany Medical Center Hospital · US

Funding

REGULATION OF B CELL FUNCTION BY INTERLEUKIN 12R01AI041715 · NIAID · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI METZGER, DENNIS W · 1998 to 2011
$4.0M
NIAID NIH HHS R01 AI041715NIAID NIH HHS R01 AI41715
6 · The paper itself

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) is a common pathogen associated with nosocomial pneumonia and is an increasing threat for severe community-acquired pneumonia. We have now investigated the role of interleukin-12 (IL-12) in protective immunity against lung infection with MRSA. The importance of IL-12 in protection from pulmonary MRSA infection was demonstrated by the finding that IL-12p35-deficient mice had a lower survival rate, higher bacterial burdens in lung and spleen, and decreased expression of interferon gamma (IFN-γ) in the lung compared to wild-type mice. These effects were completely reversed by replacement intranasal therapy with recombinant IL-12. Furthermore, exogenous IL-12 treatment of wild-type mice 24 h before pulmonary challenge with a lethal dose of MRSA significantly improved bacterial clearance and resulted in protection from death. The IL-12-treated mice had increased numbers of lung natural killer (NK) cells and neutrophils and higher levels of IFN-γ in the lung and serum compared to untreated mice. The major source of IL-12-driven IFN-γ expression in the lung was the NK cell, and the direct target of pulmonary IFN-γ was the lung macrophage, as shown using mice with a macrophage-specific defect in interferon gamma (IFN-γ) signaling (MIIG mice). Importantly, combination therapy with linezolid and IL-12 following intranasal MRSA infection significantly increased survival compared to that of mice receiving linezolid or IL-12 alone. These results indicate that IL-12-based immunotherapy may hold promise for treatment of MRSA pneumonia.

Indexed as

AnimalsAnti-Bacterial AgentsDrug Therapy, CombinationFemaleGene Expression RegulationInterferon-gammaInterleukin-12 Subunit p35LinezolidLungMacrophages, AlveolarMaleMethicillin-Resistant Staphylococcus aureusMiceMice, Inbred C57BLMice, KnockoutNeutrophilsAnti-Bacterial AgentsInterferon-gammaInterleukin-12 Subunit p35Linezolid

Identifiers

PMID26248370
PMCPMC4576051
OpenAlexW1958618378

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.