Evidence map›Paper›PMID 32185878›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2020

Evidence for the alloimmune basis and prognostic significance of Borderline T cell-mediated rejection.

Chris Wiebe, David N Rush, Ian W Gibson, Denise Pochinco, Patricia E Birk, Aviva Goldberg, Tom Blydt-Hansen, Martin Karpinski, Jamie Shaw, Julie Ho and 1 more

Registry-linked trialOpen access · bronzeAbstract 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, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06474273 (A Multicenter Randomized Controlled Trial to Treat Acute t Cell Mediated Rejection in Kidney and Kidney-pancreas Transplant Recipients), which is not on this map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
9.2field-weighted citation impact, top 1% 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.

NCT06474273 phase3recruitingnot on this mapstarted 2026, after this paper: background citation

A Multicenter Randomized Controlled Trial to Treat Acute t Cell Mediated Rejection in Kidney and Kidney-pancreas Transplant Recipients

TypeinterventionalSponsorUniversity of SydneyRan2026 to 2030Enrolled540ConditionsRejection, Transplant, Kidney, Rejection, Transplant, PancreasArmsMethylprednisolone, Prednisone
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Effectiveness of T cell-mediated rejection therapy: A systematic review and meta-analysis.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Pooled it
  2. Pharmacokinetics, lineage identity, and trafficking of ex vivo expanded polyclonal regulatory T cells in a prospective randomized clinical trial of kidney transplant recipients with allograft inflammation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Trial
  3. Trial
  4. Article
  5. Diagnostic Potential of Urine CXCL10 and Donor-Derived cfDNA in Kidney Transplant Rejection.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Frontiers in immunology · 2025
    Article
  10. Review
  11. Current Therapies in Kidney Transplant Rejection.Journal of clinical medicine · 2023
    Review
  12. Article
  13. Review
  14. The negative impact of T cell-mediated rejection on renal allograft survival in the modern era.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Observational
  15. Evolution of the Definition of Rejection in Kidney Transplantation and Its Use as an Endpoint in Clinical Trials.Transplant international : official journal of the European Society for Organ Transplantation · 2022
    Article
  16. Article
  17. 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
  18. Article
  19. Proposed Definitions of T Cell-Mediated Rejection and Tubulointerstitial Inflammation as Clinical Trial Endpoints in Kidney Transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2022
    Article
  20. The natural history ofFrontiers in medicine · 2022
    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

11 authors at 3 institutions in 1 country.

Chris WiebeDepartment of Medicine, University of Manitoba, Winnipeg, Canada.ORCID 0000-0002-1006-3545
David N RushDepartment of Medicine, University of Manitoba, Winnipeg, Canada.ORCID 0000-0002-3451-9447
Ian W GibsonShared Health Services Manitoba, Winnipeg, Canada.
Denise PochincoShared Health Services Manitoba, Winnipeg, Canada.
Patricia E BirkDepartment of Pediatrics and Child Health, University of Manitoba, Winnipeg, Canada.
Aviva GoldbergDepartment of Pediatrics and Child Health, University of Manitoba, Winnipeg, Canada.
Tom Blydt-HansenDepartment of Pediatrics, University of British Columbia, Winnipeg, Canada.
Martin KarpinskiDepartment of Medicine, University of Manitoba, Winnipeg, Canada.
Jamie ShawDepartment of Medicine, University of Manitoba, Winnipeg, Canada.
Julie HoDepartment of Medicine, University of Manitoba, Winnipeg, Canada.
Peter W NickersonDepartment of Medicine, University of Manitoba, Winnipeg, Canada.
University of Manitoba · CAManitoba Health · CAUniversity of British Columbia · CA

Funding

CIHR
6 · The paper itself

Abstract

Prognostic biomarkers of T cell-mediated rejection (TCMR) have not been adequately studied in the modern era. We evaluated 803 renal transplant recipients and correlated HLA-DR/DQ molecular mismatch alloimmune risk categories (low, intermediate, high) with the severity, frequency, and persistence of TCMR. Allograft survival was reduced in recipients with Banff Borderline (hazard ratio [HR] 2.4, P = .003) and Banff ≥ IA TCMR (HR 4.3, P < .0001) including a subset who never developed de novo donor-specific antibodies (P = .002). HLA-DR/DQ molecular mismatch alloimmune risk categories were multivariate correlates of Banff Borderline and Banff ≥ IA TCMR and correlated with the severity and frequency of rejection episodes. Recipient age, HLA-DR/DQ molecular mismatch category, and cyclosporin vs tacrolimus immunosuppression were independent correlates of Banff Borderline and Banff ≥ IA TCMR. In the subset treated with tacrolimus (720/803) recipient age, HLA-DR/DQ molecular mismatch category, and tacrolimus coefficient of variation were independent correlates of TCMR. The correlation of HLA-DR/DQ molecular mismatch category with TCMR, including Borderline, provides evidence for their alloimmune basis. HLA-DR/DQ molecular mismatch may represent a precise prognostic biomarker that can be applied to tailor immunosuppression or design clinical trials based on individual patient risk.

Indexed as

Graft RejectionKidney TransplantationGraft SurvivalHistocompatibilityHumansPrognosisT-Lymphocytesclinical research / practicegraft survivalhistocompatibilityimmunosuppression / immune modulationkidney transplantation / nephrologymajor histocompatibility complex (MHC)risk assessment / risk stratificationT cell-mediated rejection (TCMR)

Identifiers

PMID32185878
PMCPMC7496654
OpenAlexW3010810769

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.