Evidence map›Paper›PMID 41164185›Full record

ArticleFrontiers in immunology2025

Elevated Th1 and terminally differentiated cytotoxic T cells with suppressed Tc17 lymphocytes in lung tissue of advanced COPD and IPF patients undergoing lung transplantation.

Irena Šarc, Matija Rijavec, Luka Dejanović, Ana Koren, Matthias Zimmermann, Hendrik J Ankersmit, Peter Korošec

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

7 authors.

Irena ŠarcUniversity Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
Matija RijavecUniversity Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
Luka DejanovićUniversity Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
Ana KorenUniversity Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
Matthias ZimmermannChristian Doppler Laboratory for Cardiac and Thoracic Diagnosis and Regeneration, Medical University of Vienna, Vienna, Austria.
Hendrik J AnkersmitChristian Doppler Laboratory for Cardiac and Thoracic Diagnosis and Regeneration, Medical University of Vienna, Vienna, Austria.
Peter KorošecUniversity Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The immunopathogenesis of end-stage chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF) remains poorly understood. Emerging evidence suggests that distinct T cell subpopulations may play critical roles in the progression of both diseases. A better understanding of these roles could provide important insights into underlying mechanisms and guide the development of targeted therapies. Methods: We performed flow cytometric analysis of explanted lung tissue from patients with advanced COPD (n = 9), IPF (n = 9), and idiopathic pulmonary arterial hypertension (IPAH, n = 3) undergoing lung transplantation. Healthy donor lung tissue (n = 7) served as controls. Results: Both COPD and IPF lungs demonstrated an increased frequency of Th1 (CXCR3 Discussion: Our findings identify disease-specific immune signatures in end-stage COPD and IPF. Th1 cell expansion together with a reduction in Tc17 and DN TRM subsets represented shared features of COPD and IPF, whereas accumulation of terminally differentiated cytotoxic CD8

Indexed as

Idiopathic Pulmonary FibrosisLungLung TransplantationPulmonary Disease, Chronic ObstructiveTh17 CellsTh1 CellsT-Lymphocytes, CytotoxicAdultAgedCell DifferentiationFemaleHumansLymphocyte ActivationMaleMiddle AgedCD8+CD28-COPDdouble-negative T cellsIPAHIPFTc17Th1

Identifiers

PMID41164185
PMCPMC12558995

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.