Evidence map›Paper›PMID 23710539›Full record

Trial reportAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2013

Gene set enrichment analysis identifies key innate immune pathways in primary graft dysfunction after lung transplantation.

E Cantu, D J Lederer, K Meyer, K Milewski, Y Suzuki, R J Shah, J M Diamond, N J Meyer, J W Tobias, D A Baldwin and 5 more

Registry-linked trialOpen access · greenAbstract readClinical TrialComparative StudyMulticenter Study
In one paragraph

Trial report in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00531921 (Correlation of Donor Proinflammatory mRNA Profiles With Early Outcomes of Thoracic and Abdominal Transplantation), which is not on this map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.9field-weighted citation impact, top 5% 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.

NCT00531921 completednot on this map

Correlation of Donor Proinflammatory mRNA Profiles With Early Outcomes of Thoracic and Abdominal Transplantation

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2007 to 2011Enrolled313ConditionsHeart Transplantation, Kidney Transplantation, Liver Transplantation, Lung Transplantation
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 73 citations in OpenAlex.

  1. Genetic variation in the prostaglandin E2 pathway is associated with primary graft dysfunction.American journal of respiratory and critical care medicine · 2014
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. The Lung Allograft Microbiome Associates with Pepsin, Inflammation, and Primary Graft Dysfunction.American journal of respiratory and critical care medicine · 2022
    Article
  8. Article
  9. Article
  10. Primary graft dysfunction: what we know.Journal of thoracic disease · 2021
    Review
  11. Article
  12. The NLRP3 Inflammasome: Relevance in Solid Organ Transplantation.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Review
  15. Article
  16. International Society for Heart and Lung Transplantation consensus statement for the standardization of bronchoalveolar lavage in lung transplantation.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2020
    Article
  17. PreprocurementAmerican journal of respiratory and critical care medicine · 2020
    Article
  18. Article
  19. Review
  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

15 authors at 3 institutions in 1 country.

E CantuDepartment of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. edward.cantu@uphs.upenn.edu
D J Lederer
K Meyer
K Milewski
Y Suzuki
R J Shah
J M Diamond
N J Meyer
J W Tobias
D A Baldwin
V M Van Deerlin
K M Olthoff
A Shaked
J D Christie
CTOT Investigators
University of Pennsylvania · USColumbia University · USUniversity of Wisconsin–Madison · US

Funding

Molecular profiling and immunomodulatory interventionsU01AI063589 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI SHAKED, ABRAHAM NA · 2004 to 2009
$14.4M
Clinical Risk Factors for Primary Graft DysfunctionR01HL087115 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D · 2007 to 2017
$7.1M
Genetics of primary graft dysfunctionR01HL081619 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D · 2007 to 2011
$3.9M
Obesity, Inflammation, and Lung Injury After Lung TransplantationR01HL114626 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHRISTIE, JASON D, LEDERER, DAVID J. · 2013 to 2016
$3.1M
Role of anti-Col (V) immunity in primary graft dysfunctionR01HL096845 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D, WILKES, DAVID S · 2010 to 2013
$2.2M
Career Development for Genomic/Genetic Studies in Lung DiseasesK12HL090021 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI PACK, ALLAN I · 2007 to 2012
$2.0M
Mentored Patient Oriented Research in Lung TransplantationK24HL115354 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D · 2012 to 2021
$1.2M
Lung Transplant donor: prediction, evaluation, and mechanismK23HL116656 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CANTU, EDWARD · 2013 to 2017
$872k
NHLBI NIH HHS HL081619NHLBI NIH HHS HL087115NHLBI NIH HHS HL090021NHLBI NIH HHS HL096845NHLBI NIH HHS HL116656NHLBI NIH HHS K12 HL090021NHLBI NIH HHS K23 HL116656NHLBI NIH HHS K24 HL115354NHLBI NIH HHS R01 HL081619NHLBI NIH HHS R01 HL087115NHLBI NIH HHS R01 HL096845NHLBI NIH HHS R01 HL114626NIAID NIH HHS AI063589NIAID NIH HHS U01 AI063589
6 · The paper itself

Abstract

We hypothesized alterations in gene expression could identify important pathways involved in transplant lung injury. Broncho alveolar lavage fluid (BALF) was sampled from donors prior to procurement and in recipients within an hour of reperfusion as part of the NIAID Clinical Trials in Organ Transplantation Study. Twenty-three patients with Grade 3 primary graft dysfunction (PGD) were frequency matched with controls based on donor age and recipient diagnosis. RNA was analyzed using the Human Gene 1.0 ST array. Normalized mRNA expression was transformed and differences between donor and postreperfusion values were ranked then tested using Gene Set Enrichment Analysis. Three-hundred sixty-two gene sets were upregulated, with eight meeting significance (familywise-error rate, FWER p-value <0.05), including the NOD-like receptor inflammasome (NLR; p < 0.001), toll-like receptors (TLR; p < 0.001), IL-1 receptor (p = 0.001), myeloid differentiation primary response gene 88 (p = 0.001), NFkB activation by nontypeable Haemophilus influenzae (p = 0.001), TLR4 (p = 0.008) and TLR 9 (p = 0.018). The top five ranked individual transcripts from these pathways based on rank metric score are predominantly present in the NLR and TLR pathways, including IL1β (1.162), NLRP3 (1.135), IL1α (0.952), IL6 (0.931) and CCL4 (0.842). Gene set enrichment analyses implicate inflammasome-mediated and innate immune signaling pathways as key mediators of the development of PGD in lung transplant patients.

Indexed as

AdultFemaleFollow-Up StudiesGraft SurvivalHumansImmunity, InnateLung TransplantationMaleMiddle AgedPostoperative PeriodPrimary Graft DysfunctionProspective Studies

Identifiers

PMID23710539
PMCPMC3954988
OpenAlexW1825548051

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

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.