Evidence map›Paper›PMID 39779317›Full record

Observational studyJournal of clinical pathology2025

Airway associated inflammation in post-transplant cystic fibrosis patients as a predictor of chronic lung allograft dysfunction (CLAD).

Tanvi Patel, Bradford Bemiss, Elnaz Panah, Thanchanok Chaiprasit, Austin McHenry, Girish Venkataraman, Vijayalakshmi Ananthanarayanan

Abstract readObservational Study
In one paragraph

Observational study in Journal of clinical pathology, 2025. 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

7 authors.

Tanvi PatelLoyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA tpatel32@luc.edu.ORCID http://orcid.org/0000-0003-2131-9419
Bradford BemissDepartment of Medicine (Pulmonary and Critical Care), Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID http://orcid.org/0000-0003-2877-4174
Elnaz PanahDepartment of Pathology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA.
Thanchanok ChaiprasitDepartment of Pathology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA.
Austin McHenryDepartment of Pathology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA.
Girish VenkataramanDepartment of Pathology, University of Chicago Pritzker School of Medicine, Chicago, Illinois, USA.ORCID http://orcid.org/0000-0002-8674-2608
Vijayalakshmi AnanthanarayananDepartment of Pathology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA.

Funding

Summer Research Experience for Medical Students in Inflammation and Infectious DiseasesT35AI125220 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI Edward M. Campbell, Simon Kaja · 2017 to 2026
$510k
NIAID NIH HHS T35 AI125220
6 · The paper itself

Abstract

aimsIn cystic fibrosis lung transplant recipients (LTRs), graft dysfunction due to acute infections, rejection or chronic lung allograft dysfunction (CLAD) is difficult to distinguish. Characterisation of the airway inflammatory milieu could help detect and prevent graft dysfunction. We speculated that an eosinophil or neutrophil-rich milieu is associated with higher risk of CLAD.

methodsA retrospective, single-centre observational study of cystic fibrosis LTRs between 2002 and 2021 was performed. Data from biopsy slides, pulmonary function testing and bronchoalveolar lavage fluid microbiology tests were collected. The primary outcome was bronchiolitis obliterans syndrome (BOS) or death after transplant, with an 8-year follow-up period.

results40 patients were identified with an average age of 35.3 at first transplantation, including 5 redo lung transplants. Fungal infections were correlated with higher rejection scores (p<0.01) and survival status (p=0.027). Fungal and bacterial infection rates were reduced in later transplants (2014-2021) compared with earlier (2002-2014). Fungal infections were associated with significantly worsened outcomes (p≤0.001). Eosinophils in large airways was associated with worse BOS-free survival (p=0.03).

conclusionsSubcategorisation of the inflammatory milieu (particularly noting eosinophils) in surveillance biopsies may help detect CLAD earlier and improve long-term outcomes in cystic fibrosis LTRs.

Indexed as

Bronchiolitis ObliteransCystic FibrosisGraft RejectionInflammationLung TransplantationAdolescentAdultAllograftsChronic DiseaseEosinophilsFemaleHumansMaleMiddle AgedNeutrophilsRetrospective StudiesBRONCHIOLITISEOSINOPHILSGraft RejectionLUNG TRANSPLANTATION

Identifiers

PMID39779317
PMCPMC12051460

What OpenQuestion holds

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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.