Evidence map›Paper›PMID 25350513›Full record

ArticleJournal of visualized experiments : JoVE2014

Mouse kidney transplantation: models of allograft rejection.

George H Tse, Emily E Hesketh, Michael Clay, Gary Borthwick, Jeremy Hughes, Lorna P Marson

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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.

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

11 citing papers in PubMed.

  1. Article
  2. Article
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  4. Senescence-induced p21Cell discovery · 2025
    Article
  5. Article
  6. Helper T Cell (CD4Research (Washington, D.C.) · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. A mouse model of renal ischemia-reperfusion injury solely induced by cold ischemia.American journal of physiology. Renal physiology · 2019
    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

6 authors.

George H TseMRC Centre for Inflammation Research, The Queen's Medical Research Institute, The University of Edinburgh; georgetse@doctors.org.uk.
Emily E HeskethMRC Centre for Inflammation Research, The Queen's Medical Research Institute, The University of Edinburgh.
Michael ClayMRC Centre for Inflammation Research, The Queen's Medical Research Institute, The University of Edinburgh.
Gary BorthwickMRC Centre for Inflammation Research, The Queen's Medical Research Institute, The University of Edinburgh.
Jeremy HughesMRC Centre for Inflammation Research, The Queen's Medical Research Institute, The University of Edinburgh.
Lorna P MarsonMRC Centre for Inflammation Research, The Queen's Medical Research Institute, The University of Edinburgh.

Funding

Medical Research Council G0901697
6 · The paper itself

Abstract

Rejection of the transplanted kidney in humans is still a major cause of morbidity and mortality. The mouse model of renal transplantation closely replicates both the technical and pathological processes that occur in human renal transplantation. Although mouse models of allogeneic rejection in organs other than the kidney exist, and are more technically feasible, there is evidence that different organs elicit disparate rejection modes and dynamics, for instance the time course of rejection in cardiac and renal allograft differs significantly in certain strain combinations. This model is an attractive tool for many reasons despite its technical challenges. As inbred mouse strain haplotypes are well characterized it is possible to choose donor and recipient combinations to model acute allograft rejection by transplanting across MHC class I and II loci. Conversely by transplanting between strains with similar haplotypes a chronic process can be elicited were the allograft kidney develops interstitial fibrosis and tubular atrophy. We have modified the surgical technique to reduce operating time and improve ease of surgery, however a learning curve still needs to be overcome in order to faithfully replicate the model. This study will provide key points in the surgical procedure and aid the process of establishing this technique.

Indexed as

Disease Models, AnimalAllograftsAnimalsGraft RejectionKidney TransplantationMaleMiceMice, Inbred C57BLTransplantation, Homologous

Identifiers

PMID25350513
PMCPMC4540093

What OpenQuestion holds

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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.