Evidence map›Paper›PMID 39737183›Full record

ArticleFrontiers in immunology2024

Immunological characterization of pleural effusions in pediatric patients.

Luca Flögel, Elisabeth Kaiser, Muriel Charlotte Hans, Sybelle Goedicke-Fritz, Michelle Bous, Hashim Abdul-Khaliq, Martin Poryo, Michael Zemlin, Regine Weber

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Luca FlögelDepartment of General Pediatrics and Neonatology, Saarland University, Campus Homburg, Homburg, Germany.
Elisabeth KaiserDepartment of General Pediatrics and Neonatology, Saarland University, Campus Homburg, Homburg, Germany.
Muriel Charlotte HansDepartment of General Pediatrics and Neonatology, Saarland University, Campus Homburg, Homburg, Germany.
Sybelle Goedicke-FritzDepartment of General Pediatrics and Neonatology, Saarland University, Campus Homburg, Homburg, Germany.
Michelle BousDepartment of General Pediatrics and Neonatology, Saarland University, Campus Homburg, Homburg, Germany.
Hashim Abdul-KhaliqDepartment of Pediatric Cardiology, Saarland University Medical Center, Homburg, Germany.
Martin PoryoDepartment of Pediatric Cardiology, Saarland University Medical Center, Homburg, Germany.
Michael ZemlinDepartment of General Pediatrics and Neonatology, Saarland University, Campus Homburg, Homburg, Germany.
Regine WeberDepartment of General Pediatrics and Neonatology, Saarland University, Campus Homburg, Homburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The pleural cavity represents a unique immunological compartment that can mount inflammatory reactions during infections, after surgery and in chronic immunological diseases. The connection between systemic immune reactions in the blood and local immune reactions in pleural effusions remains unclear. This study provides the first comprehensive immunological characterization of paired blood and pleural effusion samples, utilizing combined cell and cytokine analyses in pediatric patients undergoing cardiac surgery. Methods: In 30 pediatric patients (median age: 22 months) with pleural effusion after cardiac surgery for congenital heart defects, corresponding peripheral blood and pleural effusion samples were analyzed for their immune response. We used flow cytometry and multiplex immunoassays to quantify 14 T cell subpopulations and 12 T cell associated cytokines in each biosample. Results: IL-6, IL-8, IL-10, TNF (p<0.0001) levels were significantly higher in pleural effusion compared to plasma. In contrast, IFN-γ, GM-CSF, IL-17A levels were lower in pleural effusion than in plasma (p ≤ 0.0005). In comparison to peripheral blood, there was a significantly higher proportion of T helper cells 1 (T Conclusion: Immunological factors in pleural effusions differed significantly from the corresponding blood samples in pediatric patients after cardiac surgery. The results suggest localized production of specific cytokines within the pleural space, while the distribution of other cytokines in pleural effusions appears to be more reflective of the systemic immune response. We found evidence that on the cellular level, the surface marker CD62L may play a key role in navigating T cells between the blood and pleural effusion. This study confirms that the pleural cavity harbors a unique lymphatic compartment, the analysis of which may be useful for both diagnostic and therapeutic purposes.

Indexed as

CytokinesPleural EffusionChildChild, PreschoolFemaleHeart Defects, CongenitalHumansInfantMaleT-Lymphocyte SubsetsCytokinescardiac surgeryneonatespediatricspleural effusionT cells immunology differentiation

Identifiers

PMID39737183
PMCPMC11682977

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.