Evidence map›Paper›PMID 38375427›Full record

ArticleERJ open research2024

Aberrant characteristics of peripheral blood innate lymphoid cells in COPD, independent of smoking history.

Cathelijne M van Zelst, Johannes C C M In 't Veen, Lisette Krabbendam, Geertje M de Boer, Marjolein J W de Bruijn, Menno van Nimwegen, Esmee K van der Ploeg, Denise van Uden, Ralph Stadhouders, Gerdien A Tramper-Stranders and 2 more

Abstract read
In one paragraph

Article in ERJ open research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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

12 authors.

Cathelijne M van ZelstDepartment of Pulmonology, Franciscus Gasthuis and Vlietland, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-9221-7439
Johannes C C M In 't VeenDepartment of Pulmonology, Franciscus Gasthuis and Vlietland, Rotterdam, the Netherlands.
Lisette KrabbendamDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Geertje M de BoerDepartment of Pulmonology, Franciscus Gasthuis and Vlietland, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-9615-1123
Marjolein J W de BruijnDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Menno van NimwegenDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Esmee K van der PloegDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Denise van UdenDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Ralph StadhoudersDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Gerdien A Tramper-StrandersDepartment of Pulmonology, Franciscus Gasthuis and Vlietland, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-0228-5375
Rudi W HendriksDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Gert-Jan BraunstahlDepartment of Pulmonology, Franciscus Gasthuis and Vlietland, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0001-7671-3742

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Distinguishing asthma and COPD can pose challenges in clinical practice. Increased group 1 innate lymphoid cells (ILC1s) have been found in the lungs and peripheral blood of COPD patients, while asthma is associated with elevated levels of ILC2s. However, it is unclear whether the inflammatory characteristics of ILC1s and ILC2s differ between COPD and asthma. This study aims to compare peripheral blood ILC subsets and their expression of inflammatory markers in COPD patients, asthma patients and controls. Methods: The study utilised multi-colour flow cytometry to analyse peripheral blood ILC populations in clinically stable COPD patients (n=38), asthma patients (n=37), and smoking (n=19) and non-smoking (n=16) controls. Results: Proportions of peripheral blood inflammatory CD4 Conclusion: Our in-depth characterisation of ILC1 and ILC2 populations in peripheral blood revealed significant differences in their phenotypes between COPD and asthma patients and smoking or non-smoking controls. These findings suggest a role for both ILC subsets in COPD disease pathology, independent of smoking history, and may have implications for patient stratification and therapy development.

Identifiers

PMID38375427
PMCPMC10875467

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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.