Evidence map›Paper›PMID 25855773›Full record

ArticleJournal of the American Society of Nephrology : JASN2015

Dendritic Cells in Kidney Transplant Biopsy Samples Are Associated with T Cell Infiltration and Poor Allograft Survival.

Ibrahim Batal, Sacha A De Serres, Kassem Safa, Vanesa Bijol, Takuya Ueno, Maristela L Onozato, A John Iafrate, Jan M Herter, Andrew H Lichtman, Tanya N Mayadas and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Sensitization in Transplantation Assessment of Risk 2025 innate working group: The potential role of innate allorecognition in kidney allograft damage.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Review
  2. Human type 1 conventional dendritic cells contribute to skin transplant rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Deciphering the Complexity of the Immune Cell Landscape in Kidney Allograft Rejection.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Review
  7. Review
  8. Article
  9. The clinical significance of receiving a kidney allograft from deceased donor with chronic histologic changes.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Innate allorecognition by monocytic cells and its role in graft rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2018
    Review
  16. Review
  17. Article
  18. Article
  19. Current status of alloimmunity.Current opinion in nephrology and hypertension · 2016
    Review
  20. 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

14 authors at 3 institutions in 1 country.

Ibrahim BatalDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts; ib234@columbia.edu.
Sacha A De SerresRenal Division, Schuster Family Transplantation Research Center, Brigham and Women's Hospital, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts; and.
Kassem SafaRenal Division, Schuster Family Transplantation Research Center, Brigham and Women's Hospital, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts; and.
Vanesa BijolDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts;
Takuya UenoRenal Division, Schuster Family Transplantation Research Center, Brigham and Women's Hospital, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts; and.
Maristela L OnozatoDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
A John IafrateDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Jan M HerterDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts;
Andrew H LichtmanDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts;
Tanya N MayadasDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts;
Indira GuleriaRenal Division, Schuster Family Transplantation Research Center, Brigham and Women's Hospital, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts; and.
Helmut G RennkeDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts;
Nader NajafianRenal Division, Schuster Family Transplantation Research Center, Brigham and Women's Hospital, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts; and.
Anil ChandrakerRenal Division, Schuster Family Transplantation Research Center, Brigham and Women's Hospital, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts; and.
Harvard University · USBrigham and Women's Hospital · USMassachusetts General Hospital · US

Funding

Novel Therapies to Improve Renal and Cardiac Allograft OutcomesU01AI063623 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI CHANDRAKER, ANIL · 2004 to 2013
$30.9M
TNFR2 Regulation of Leukocyte Recruitment in GlomerulonephritisR01DK099507 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI MAYADAS, TANYA N · 2014 to 2018
$2.1M
Canadian Institutes of Health Research KRI123890NIAID NIH HHS U01 AI063623NIAID NIH HHS U01-AI 063623NIDDK NIH HHS R01 DK099507NIDDK NIH HHS R01-DK099507
6 · The paper itself

Abstract

Progress in long-term renal allograft survival continues to lag behind the progress in short-term transplant outcomes. Dendritic cells are the most efficient antigen-presenting cells, but surprisingly little attention has been paid to their presence in transplanted kidneys. We used dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin as a marker of dendritic cells in 105 allograft biopsy samples from 105 kidney transplant recipients. High dendritic cell density was associated with poor allograft survival independent of clinical variables. Moreover, high dendritic cell density correlated with greater T cell proliferation and poor outcomes in patients with high total inflammation scores, including inflammation in areas of tubular atrophy. We then explored the association between dendritic cells and histologic variables associated with poor prognosis. Multivariate analysis revealed an independent association between the densities of dendritic cells and T cells. In biopsy samples with high dendritic cell density, electron microscopy showed direct physical contact between infiltrating lymphocytes and cells that have the ultrastructural morphologic characteristics of dendritic cells. The origin of graft dendritic cells was sought in nine sex-mismatched recipients using XY fluorescence in situ hybridization. Whereas donor dendritic cells predominated initially, the majority of dendritic cells in late allograft biopsy samples were of recipient origin. Our data highlight the prognostic value of dendritic cell density in allograft biopsy samples, suggest a new role for these cells in shaping graft inflammation, and provide a rationale for targeting dendritic cell recruitment to promote long-term allograft survival.

Indexed as

Graft SurvivalKidney TransplantationAdultAllograftsBiopsyCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsFemaleHumansKidneyLectins, C-TypeMaleMicroscopy, ElectronMiddle AgedNephritisCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinLectins, C-TypeReceptors, Cell Surfacechronic graft deteriorationchronic inflammationtransplant pathology

Identifiers

PMID25855773
PMCPMC4657833
OpenAlexW2121236840

What OpenQuestion holds

Textmetadata
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.