Evidence map›Paper›PMID 40523479›Full record

ReviewAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2025

Mouse orthotopic liver transplantation: Challenges, achievements, and applications.

Shinichiro Yokota, Wei Li, Pierre A Clavien, Jerzy W Kupiec-Weglinski, Angus W Thomson

Abstract readReview
In one paragraph

Review in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Shinichiro YokotaDivision of Abdominal Transplant, Department of Surgery, Stanford University School of Medicine, Stanford, California, USA.
Wei LiDepartment of Hepatobiliary-Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China.
Pierre A ClavienWyss Translational Center, University of Zurich, Zurich, Switzerland.
Jerzy W Kupiec-WeglinskiDivision of Liver and Pancreas Transplantation, Department of Surgery, Dumont-UCLA Transplantation Center, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Angus W ThomsonDepartment of Surgery, Starzl Transplantation Institute, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA. Electronic address: thomsonaw@upmc.edu.

Funding

Regulation of Innate Immune Responses by Alloimmunity in Liver Ischemia-Reperfusion InjuryP01AI120944 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ELAINE F REED · 2017 to 2026
$20.0M
Liver Antigen - Presenting Cells in Hepatic Injury and TransplantationP01AI081678 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2009 to 2010
$2.8M
Regulation of Liver DC Function and Transplant ToleranceR01AI118777 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2017 to 2021
$2.3M
LIVER TRANSPLANTATION: THE ROLE OF DENDRITIC CELLSR01DK049745 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 1996 to 2005
$1.4M
Plasmacytoid Dendritic Cells and Transplant ToleranceR01AI060994 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2005 to 2008
$1.1M
NIAID NIH HHS P01 AI081678NIAID NIH HHS P01 AI120944NIAID NIH HHS R01 AI060994NIAID NIH HHS R01 AI118777NIDDK NIH HHS R01 DK049745
6 · The paper itself

Abstract

The surgically challenging mouse orthotopic liver transplant model has provided numerous insights into liver immunobiology, cellular and molecular regulation of liver transplant ischemia-reperfusion injury, liver regeneration, the influence of major histocompatibility complex antigens on transplant outcome, spontaneous transplant tolerance, and regulation of allograft immunity. Nonarterialized and arterialized models have been established. Reduced-size liver transplant models have also been developed and used to determine critical mass and factors that determine tissue injury and regeneration. Since its first description 3 decades ago, the surgical demands of the model have limited its application to a relatively small number of centers focused on basic liver transplant research. Dissemination of and commitment to acquisition of the required technical skills will facilitate the application of cutting-edge experimental approaches to which the mouse model is well-suited and allow important key basic and translational questions in transplant immunology to be addressed.

Indexed as

Liver TransplantationAnimalsDisease Models, AnimalGraft RejectionGraft SurvivalHumansLiver RegenerationMiceReperfusion Injuryallograft rejectionischemia-reperfusion injuryliver regenerationliver transplantationmousesurgical modeltransplant tolerance

Identifiers

PMID40523479
PMCPMC13222681

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.