Evidence map›Paper›PMID 40726990›Full record

ReviewJHLT open2025

Telomere biology disorders in lung transplantation: Clinical challenges and management strategies.

Farah Mesli, Quentin Philippot, Kinan El Husseini, Vincent Bunel, Caroline Kannengiesser, Marie Pierre Debray, Alice Guyard, Bruno Crestani, Ibrahima Ba, Raphaël Borie

Abstract readReview
In one paragraph

Review in JHLT open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Post-lung transplant surveillance in 2026: current practice, variability, and the need for standardization.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Review
  2. Review
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

10 authors.

Farah MesliService de Pneumologie, Allergologie et Transplantation, Hôpital Bichat Claude Bernard, APHP, Centre de Référence des Maladies Pulmonaires Rares, Paris, France.
Quentin PhilippotService de Pneumologie, Allergologie et Transplantation, Hôpital Bichat Claude Bernard, APHP, Centre de Référence des Maladies Pulmonaires Rares, Paris, France.
Kinan El HusseiniService de Pneumologie, Allergologie et Transplantation, Hôpital Bichat Claude Bernard, APHP, Centre de Référence des Maladies Pulmonaires Rares, Paris, France.
Vincent BunelService de Pneumologie, Allergologie et Transplantation, Hôpital Bichat Claude Bernard, APHP, Centre de Référence des Maladies Pulmonaires Rares, Paris, France.
Caroline KannengiesserUniversité Paris Cité, Inserm U1149, Centre de Recherche sur l'Inflammation, Université Paris Cité, Paris, France.
Marie Pierre DebrayUniversité Paris Cité, Inserm U1149, Centre de Recherche sur l'Inflammation, Université Paris Cité, Paris, France.
Alice GuyardService de Pathologie, Hôpital Bichat Claude Bernard, APHP, Paris, France.
Bruno CrestaniService de Pneumologie, Allergologie et Transplantation, Hôpital Bichat Claude Bernard, APHP, Centre de Référence des Maladies Pulmonaires Rares, Paris, France.
Ibrahima BaUniversité Paris Cité, Inserm U1149, Centre de Recherche sur l'Inflammation, Université Paris Cité, Paris, France.
Raphaël BorieService de Pneumologie, Allergologie et Transplantation, Hôpital Bichat Claude Bernard, APHP, Centre de Référence des Maladies Pulmonaires Rares, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomeres, repetitive DNA sequences at the ends of chromosomes, play a crucial role in maintaining genomic stability. In recent years, their significance in lung transplantation has gained growing attention. Shortened telomeres-whether due to inherited telomeropathies or acquired attrition-have emerged as a risk factor for various pulmonary diseases, particularly pulmonary fibrosis, which is a leading indication for lung transplantation. This review provides a comprehensive overview of current knowledge on the impact of short telomeres in lung transplant recipients, encompassing pre-transplant assessment and post-transplant outcomes. Patients with telomere-biology disorder present unique clinical challenges. Before transplantation, they may exhibit extra-pulmonary manifestations such as bone marrow dysfunction, hepatic abnormalities, precipitation to develop cancer, all of which necessitate a tailored evaluation and multidisciplinary management. After transplantation, these patients appear to be at increased risk of complications, including drug-related hematologic toxicity, bone marrow failure, and heightened susceptibility to infections. The review emphasizes the importance of identifying patients with telomere biology disorders early in the transplant process and supports the incorporation of telomere length testing in selected populations. Furthermore, it highlights the need for adjusted immunosuppressive strategies and closer surveillance in this vulnerable population. Ultimately, the authors advocate for prospective, multicenter studies aimed at refining the prognostic value of telomere length and guiding evidence-based, individualized transplant strategies for patients with telomere biology disorders related interstitial lung diseases.

Indexed as

familial pulmonary fibrosisgeneticinterstitial lung diseaseslung transplantationoutcomestelomere

Identifiers

PMID40726990
PMCPMC12301819

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.