Evidence map›Paper›PMID 39935537›Full record

ArticleFrontiers in cellular and infection microbiology2024

Corynebacteria from the respiratory microbiota modulate inflammatory responses and associate with a reduced pneumococcal burden in the lungs.

Caroline Bergenfelz, Phuong Do, Liv Larsson, Hanna Ivarsson, Kasper Malmborn, Anders P Håkansson

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Association of nasopharyngealMicrobiology spectrum · 2026
    Article
  3. Article
  4. Article
  5. 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

6 authors.

Caroline BergenfelzDepartment of Translational Medicine, Division of Experimental Infection Medicine, Lund University, Lund, Sweden.
Phuong Do *Department of Translational Medicine, Division of Experimental Infection Medicine, Lund University, Lund, Sweden.
Liv Larsson *Department of Translational Medicine, Division of Experimental Infection Medicine, Lund University, Lund, Sweden.
Hanna IvarssonDepartment of Translational Medicine, Division of Experimental Infection Medicine, Lund University, Lund, Sweden.
Kasper MalmbornDepartment of Translational Medicine, Division of Experimental Infection Medicine, Lund University, Lund, Sweden.
Anders P HåkanssonDepartment of Translational Medicine, Division of Experimental Infection Medicine, Lund University, Lund, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Certain species from the normal respiratory tract microbiota have recently been proposed to positively influence human health. Method: Respiratory tract epithelial cells NCI-H292 and BALB/cByJ mice were inoculated with Corynebacteria ( Results: Clinical isolates of Corynebacteria were well tolerated by human cells and mice. Corynebacteria induced a transient inflammatory response during healthy conditions in the absence of known pathogens. Pre-exposure or nasal priming with Corynebacteria did not affect subsequent acquisition of pneumococci but were associated with a modulated inflammatory response Conclusions: In this study, we delineate the role of Corynebacteria from the normal microbiota that epidemiologically associate with respiratory health. We show that the presence of Corynebacteria modulates the inflammatory response to pneumococci and associate with faster decrease in pneumococcal burden, primarily in the lower respiratory tract. Our data indicate that Corynebacteria has potential to protect against severe pneumococcal infections.

Indexed as

CorynebacteriumCorynebacterium InfectionsInflammationLungMicrobiotaPneumococcal InfectionsRespiratory Tract InfectionsStreptococcus pneumoniaeAnimalsBacterial LoadCell LineCytokinesDisease Models, AnimalEpithelial CellsFemaleHumansCytokinescorynebacteriainflammationmicrobiotapneumoniarespiratory tractStreptococcus pneumoniae

Identifiers

PMID39935537
PMCPMC11811110

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Registered trials

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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.