Evidence map›Paper›PMID 37295720›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2023

Defining a natural killer cell-enriched molecular rejection-like state in lung transplant transbronchial biopsies.

Patrick T Gauthier, Martina Mackova, Alim Hirji, Justin Weinkauf, Irina L Timofte, Greg I Snell, Glen P Westall, Jan Havlin, Robert Lischke, Andrea Zajacová and 12 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02812290 (Multi-Centric Observational Study to Analyze the Diagnostic Molecular Features in the Clinical Setting of Lung Allograft Biopsies), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT02812290 recruitingnot on this map

Multi-Centric Observational Study to Analyze the Diagnostic Molecular Features in the Clinical Setting of Lung Allograft Biopsies

TypeobservationalSponsorUniversity of AlbertaRan2016 to 2027Enrolled700ConditionsLung Transplant RejectionArmsLung transplant biopsy bites.
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Utility of donor-derived cell-free DNA testing after lung transplantation in the precision medicine era.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2026
    Review
  2. Airway molecular signatures in antibody-mediated lung transplant rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  3. 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
  4. Article
  5. Treatment Responses in Histologic Versus Molecular Diagnoses of Lung Rejection.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Article
  6. Theseus and the search for an antibody-mediated rejection molecular state in lung transplant biopsies.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Patrick T GauthierUniversity of Alberta, Edmonton, Alberta, Canada.
Martina MackovaUniversity of Alberta, Edmonton, Alberta, Canada.
Alim HirjiUniversity of Alberta, Edmonton, Alberta, Canada.
Justin WeinkaufUniversity of Alberta, Edmonton, Alberta, Canada.
Irina L TimofteUT Southwestern Medical Center, Dallas, Texas, USA.
Greg I SnellAlfred Hospital Lung Transplant Service, Melbourne, Victoria, Australia.
Glen P WestallAlfred Hospital Lung Transplant Service, Melbourne, Victoria, Australia.
Jan HavlinUniversity Hospital Motol, Prague, Czech Republic.
Robert LischkeUniversity Hospital Motol, Prague, Czech Republic.
Andrea ZajacováUniversity Hospital Motol, Prague, Czech Republic.
Jan SimonekUniversity Hospital Motol, Prague, Czech Republic.
Ramsey HachemWashington University in St Louis, St. Louis, Missouri, USA.
Daniel KreiselWashington University in St Louis, St. Louis, Missouri, USA.
Deborah LevineStanford University, Stanford, California, USA.
Bartosz KubisaPomeranian Medical University of Szczecin, Szczecin, Poland.
Maria PiotrowskaPomeranian Medical University of Szczecin, Szczecin, Poland.
Stephen JuvetToronto Lung Transplant Program, University Health Network, Toronto, Ontario, Canada.
Shaf KeshavjeeToronto Lung Transplant Program, University Health Network, Toronto, Ontario, Canada.
Peter JakschMedical University of Vienna, Vienna, Austria.
Walter KlepetkoMedical University of Vienna, Vienna, Austria.
Kieran HalloranUniversity of Alberta, Edmonton, Alberta, Canada.
Philip F HalloranUniversity of Alberta, Edmonton, Alberta, Canada. Electronic address: phallora@ualberta.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In lung transplantation, antibody-mediated rejection (AMR) diagnosed using the International Society for Heart and Lung Transplantation criteria is uncommon compared with other organs, and previous studies failed to find molecular AMR (ABMR) in lung biopsies. However, understanding of ABMR has changed with the recognition that ABMR in kidney transplants is often donor-specific antibody (DSA)-negative and associated with natural killer (NK) cell transcripts. We therefore searched for a similar molecular ABMR-like state in transbronchial biopsies using gene expression microarray results from the INTERLUNG study (#NCT02812290). After optimizing rejection-selective transcript sets in a training set (N = 488), the resulting algorithms separated an NK cell-enriched molecular rejection-like state (NKRL) from T cell-mediated rejection (TCMR)/Mixed in a test set (N = 488). Applying this approach to all 896 transbronchial biopsies distinguished 3 groups: no rejection, TCMR/Mixed, and NKRL. Like TCMR/Mixed, NKRL had increased expression of all-rejection transcripts, but NKRL had increased expression of NK cell transcripts, whereas TCMR/Mixed had increased effector T cell and activated macrophage transcripts. NKRL was usually DSA-negative and not recognized as AMR clinically. TCMR/Mixed was associated with chronic lung allograft dysfunction, reduced one-second forced expiratory volume at the time of biopsy, and short-term graft failure, but NKRL was not. Thus, some lung transplants manifest a molecular state similar to DSA-negative ABMR in kidney and heart transplants, but its clinical significance must be established.

Indexed as

Kidney TransplantationLung TransplantationAntibodiesBiopsyGraft RejectionKidneyKiller Cells, NaturalAntibodiesCLADNK cellsNKRLTBBTCMR

Identifiers

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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.