Evidence map›Paper›PMID 23447068›Full record

ArticleKidney international2013

Increased C4d in post-reperfusion biopsies and increased donor specific antibodies at one-week post transplant are risk factors for acute rejection in mild to moderately sensitized kidney transplant recipients.

Arjang Djamali, Brenda L Muth, Thomas M Ellis, Maha Mohamed, Luis A Fernandez, Karen M Miller, Janet M Bellingham, Jon S Odorico, Joshua D Mezrich, John D Pirsch and 6 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Kidney international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

NCT02133248 terminatednot on this mapstarted 2014, after this paper: background citation

Identification of Donor Specific B Cells Will Positively Affect Monitoring and Treatment of Donor Specific Antibodies and Antibody Mediated Rejection

TypeobservationalSponsorUniversity of Wisconsin, MadisonRan2014 to 2021Enrolled86ConditionsSensitized Kidney Transplant Recipients
NCT03791476 phase1unknown statusnot on this mapstarted 2019, after this paper: background citation

A Phase I/II,Single Center,Randomized,Double-Blind,Placebo-Controlled Study to Evaluate the Feasibility of Using Human Recombinant C1 Inhibitor(RUCONEST®) as a Therapeutic Strategy to Reduce the Incidence of Delayed Graft Function in Recipients of Kidneys From Donation After Cardio-Circulatory Death

TypeinterventionalSponsorUniversity of Wisconsin, MadisonRan2019 to 2022Enrolled20ConditionsKidney FailureArmsrhC1INH, Saline Solution
3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Imlifidase for Kidney Transplantation of Highly Sensitized Patients With a Positive Crossmatch: The French Consensus Guidelines.Transplant international : official journal of the European Society for Organ Transplantation · 2023
    Article
  2. Proposed Definitions of Antibody-Mediated Rejection for Use as a Clinical Trial Endpoint in Kidney Transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Isolated endarteritis and kidney transplant survival: a multicenter collaborative study.Journal of the American Society of Nephrology : JASN · 2015
    Article
  7. Review
  8. Characterization of transfusion-elicited acute antibody-mediated rejection in a rat model of kidney transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2014
    Article
  9. Diagnosis and management of antibody-mediated rejection: current status and novel approaches.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2014
    Review
  10. 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

16 authors.

Arjang DjamaliDepartment of Surgery, University of Wisconsin, Madison, Wisconsin 51703, USA. axd@medicine.wisc.edu
Brenda L Muth
Thomas M Ellis
Maha Mohamed
Luis A Fernandez
Karen M Miller
Janet M Bellingham
Jon S Odorico
Joshua D Mezrich
John D Pirsch
Tony M D'Alessandro
Vijay Vidyasagar
R Michael Hofmann
Jose R Torrealba
Dixon B Kaufman
David P Foley

Funding

Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
INSTITUTIONAL CTSA (UW-MADISON): CLINICAL TRIALSUL1RR025011 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$29.5M
The role of Nox2 in CNI-induced renal fibrosisR01DK092454 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI DJAMALI, ARJANG · 2011 to 2015
$1.7M
HSP27 in Kidney Epithelial to Mesenchymal TransformationK08DK067981 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI DJAMALI, ARJANG · 2004 to 2008
$587k
NCATS NIH HHS UL1 TR000427NCRR NIH HHS 1UL1RR025011NCRR NIH HHS UL1 RR025011NIDDK NIH HHS DK067981-5NIDDK NIH HHS K08 DK067981NIDDK NIH HHS R01 DK092454NIDDK NIH HHS R01 DK092454-01
6 · The paper itself

Abstract

In order to define the intensity of immunosuppression, we examined risk factors for acute rejection in desensitization protocols that use baseline donor-specific antibody levels measured as mean fluorescence intensity (MFImax). The study included 146 patients transplanted with a negative flow crossmatch and a mean follow-up of 18 months with the majority (83%) followed for at least 1 year. At the time of transplant, mean-calculated panel-reactive antibody and MFImax ranged from 10.3-57.2% and 262-1691, respectively, between low- and high-risk protocols. Mean MFImax increased significantly from transplant to 1 week and 1 year. The incidence of acute rejection (mean 1.65 months) as a combination of clinical and subclinical rejection was 32%, including 14% cellular, 12% antibody-mediated, and 6% mixed rejection. In regression analyses, only C4d staining in post-reperfusion biopsies (hazard ratio 3.3, confidence interval 1.71-6.45) and increased specific antibodies at 1-week post transplant were significant predictors of rejection. A rise in MFImax by 500 was associated with a 2.8-fold risk of rejection. Thus, C4d staining in post-reperfusion biopsies and an early rise in donor specific antibodies after transplantation are risk factors for rejection in moderately sensitized patients.

Indexed as

HistocompatibilityTissue DonorsAcute DiseaseAdultBiomarkersBiopsyChi-Square DistributionComplement C4bFemaleGraft RejectionHistocompatibility TestingHumansImmunosuppressive AgentsIsoantibodiesKaplan-Meier EstimateKidneyBiomarkersComplement C4bcomplement C4dImmunosuppressive AgentsIsoantibodiesPeptide Fragments

Identifiers

PMID23447068
PMCPMC3672254

What OpenQuestion holds

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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.