Evidence map›Paper›PMID 25683785›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2015

Staphylococcus via an interaction with the ELR+ CXC chemokine ENA-78 is associated with BOS.

A L Gregson, X Wang, P Injean, S S Weigt, M Shino, D Sayah, A DerHovanessian, J P Lynch, D J Ross, R Saggar and 4 more

Open access · greenAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 9% 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.

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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Prognostic implications of and clinical risk factors for acute lung injury and organizing pneumonia after lung transplantation: Data from a multicenter prospective cohort study.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  3. Plasma CXCL9 and CXCL10 at allograft injury predict chronic lung allograft dysfunction.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  4. Donor derived cell free DNA% is elevated with pathogens that are risk factors for acute and chronic lung allograft injury.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2021
    Article
  5. Correlation between BAL CXCR3 chemokines and lung allograft histopathologies: A multicenter study.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  6. Pseudomonas aeruginosa and acute rejection independently increase the risk of donor-specific antibodies after lung transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Article
  7. Review
  8. Article
  9. Article
  10. Host-Pathogen Interactions and Chronic Lung Allograft Dysfunction.Annals of the American Thoracic Society · 2017
    Article
  11. Review
  12. Article
  13. Infectious Triggers of Chronic Lung Allograft Dysfunction.Current infectious disease reports · 2016
    Review
  14. Altered Exosomal RNA Profiles in Bronchoalveolar Lavage from Lung Transplants with Acute Rejection.American journal of respiratory and critical care medicine · 2015
    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

14 authors at 1 institution in 1 country.

A L GregsonDivision of Infectious Diseases, Department of Medicine, University of California, Los Angeles, CA.
X Wang
P Injean
S S Weigt
M Shino
D Sayah
A DerHovanessian
J P Lynch
D J Ross
R Saggar
A Ardehali
G Li
R Elashoff
J A Belperio
University of California, Los Angeles · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
UCLA Center for Excellence in Pancreatic DiseasesP01AT003960 · NCCIH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HINES, OSCAR JOE · 2007 to 2011
$5.6M
Immune Mechanisms of AlloinjuryR01HL112990 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BELPERIO, JOHN A · 2012 to 2016
$2.2M
Role of T Regulatory Cells in Preventing Human BOSK23HL102220 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GREGSON, ARIC L. · 2011 to 2015
$762k
The Role of Aspergillus in the Pathogenesis of Bronchiolitis Obliterans SyndromeK23HL094746 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WEIGT, STEPHEN S · 2009 to 2013
$644k
NCATS NIH HHS UL1 TR000124NCCIH NIH HHS P01 AT003960NCCIH NIH HHS P01AT003960NCI NIH HHS CA016042NCI NIH HHS P30 CA016042NCRR NIH HHS U54 RR031268NHLBI NIH HHS K23 HL094746NHLBI NIH HHS K23 HL102220NHLBI NIH HHS R01 HL112990
6 · The paper itself

Abstract

Staphylococcus aureus is the most commonly isolated gram-positive bacterium after lung transplantation (LT) and has been associated with poor posttransplant outcomes, but its effect on bronchiolitis obliterans syndrome (BOS) and death in the context of the allograft inflammatory environment has not been studied. A three-state Cox semi-Markovian model was used to determine the influence of allograft S. aureus and the ELR+ CXC chemokines on the survival rates and cause-specific hazards for movement from lung transplant (State 1) to BOS (State 2), from transplant (State 1) to death (State 3), and from BOS (State 2) to death (State 3). Acute rejection, pseudomonas pneumonia, bronchoalveolar lavage fluid (BALF) CXCL5 and its interaction with S. aureus all increased the likelihood of transition from transplant to BOS. Transition to death from transplant was facilitated by pseudomonas infection and single lung transplant. Movement from BOS to death was affected by the interaction between aspergillus, pseudomonas and CXCL5, but not S. aureus. S. aureus isolation had state specific effects after LT and only in concert with elevated BALF CXCL5 concentrations did it augment the risk of BOS. Pseudomonas and elevated BALF concentrations of CXCL5 continued as significant risk factors for BOS and death after BOS in lung transplantation.

Indexed as

Bronchiolitis ObliteransBronchoalveolar Lavage FluidChemokine CXCL5Chemokines, CXCHumansLung TransplantationStaphylococcus aureusTreatment OutcomeChemokine CXCL5Chemokines, CXCBacterialbronchiolitis obliterans (BOS)chemokines/chemokine receptorsclinical researchimmune regulationinfection and infectious agentsinfectious diseaselung transplantationpracticepulmonologyrejection: chronicsciencetranslational research

Identifiers

PMID25683785
PMCPMC4336208
OpenAlexW1606452088

What OpenQuestion holds

Textmetadata
LicenceTDM
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.