Evidence map›Paper›PMID 31379869›Full record

ReviewFrontiers in immunology2019

Early Identification of Chronic Lung Allograft Dysfunction: The Need of Biomarkers.

Adrien Tissot, Richard Danger, Johanna Claustre, Antoine Magnan, Sophie Brouard

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07234760 (ex Vivo Study of Liposomes Loaded With Everolimus in Chronic Lung Allograft Disfunction), which is not on this map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.1field-weighted citation impact, top 2% of its field
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.

NCT07234760 completednot on this mapstarted 2022, after this paper: background citation

ex Vivo Study of Liposomes Loaded With Everolimus in Chronic Lung Allograft Disfunction

TypeobservationalSponsorFondazione IRCCS Policlinico San Matteo di PaviaRan2022 to 2025Enrolled19ConditionsBronchiolitis Obliterans Syndrome (BOS)ArmsLiposomes
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Small airway brush gene expression predicts chronic lung allograft dysfunction and mortality.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2024
    Article
  7. Article
  8. HyperpolarizedJHLT open · 2024
    Article
  9. Article
  10. Macrophage and CD8 T cell discordance are associated with acute lung allograft dysfunction progression.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2024
    Article
  11. Article
  12. Donor Fractions of Cell-Free DNA Are Elevated During CLAD But Not During Infectious Complications After Lung Transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 4 institutions in 1 country.

Adrien TissotCentre de Recherche en Transplantation et Immunologie (CRTI), INSERM, Université de Nantes, Nantes, France.
Richard DangerCentre de Recherche en Transplantation et Immunologie (CRTI), INSERM, Université de Nantes, Nantes, France.
Johanna ClaustreCentre de Recherche en Transplantation et Immunologie (CRTI), INSERM, Université de Nantes, Nantes, France.
Antoine MagnanCentre de Recherche en Transplantation et Immunologie (CRTI), INSERM, Université de Nantes, Nantes, France.
Sophie BrouardCentre de Recherche en Transplantation et Immunologie (CRTI), INSERM, Université de Nantes, Nantes, France.
Nantes Université · FRCentre Hospitalier Universitaire de Grenoble · FRInstitut de Transplantation Urologie en Nephrologie · FRInstitut du Thorax · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A growing number of patients with end-stage lung disease have benefited from lung transplantation (LT). Improvements in organ procurement, surgical techniques and intensive care management have greatly increased short-term graft survival. However, long-term outcomes remain limited, mainly due to the onset of chronic lung allograft dysfunction (CLAD), whose diagnosis is based on permanent loss of lung function after the development of irreversible lung lesions. CLAD is associated with high mortality and morbidity, and its exact physiopathology is still only partially understood. Many researchers and clinicians have searched for CLAD biomarkers to improve diagnosis, to refine the phenotypes associated with differential prognosis and to identify early biological processes that lead to CLAD to enable an early intervention that could modify the inevitable degradation of respiratory function. Donor-specific antibodies are currently the only biomarkers used in routine clinical practice, and their significance for accurately predicting CLAD is still debated. We describe here significant studies that have highlighted potential candidates for reliable and non-invasive biomarkers of CLAD in the fields of imaging and functional monitoring, humoral immunity, cell-mediated immunity, allograft injury, airway remodeling and gene expression. Such biomarkers would improve CLAD prediction and allow differential LT management regarding CLAD risk.

Indexed as

AllograftsAnimalsBiomarkersGraft RejectionHumansImmunity, CellularImmunity, HumoralLungLung TransplantationBiomarkersbiomarkerbloodBOSbronchoalveolar lavage fluidchronic lung allograft dysfunctionlung transplantationRAS

Identifiers

PMID31379869
PMCPMC6650588
OpenAlexW2954522251

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.