Evidence map›Paper›PMID 40967922›Full record

ArticleTransplantation proceedings2025

Immunological Rejection in a Heterotopic Rat Liver Transplant Model.

Camryn Thompson, Bret Verhoven, Min Zhang, Weifeng Zeng, Isaac Alderete, Ahmed Hassan, Peter Chlebeck, Kristina Matkowskyj, Heather Jennings, Andrew S Barbas and 1 more

Abstract read
In one paragraph

Article in Transplantation proceedings, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

11 authors.

Camryn ThompsonDepartment of Abdominal Transplant Surgery, Duke University School of Medicine, Durham, North Carolina.
Bret VerhovenSchool of Medicine and Public Health, Department of Surgery, University of Wisconsin-Madison, Madison, WI.
Min ZhangDepartment of Abdominal Transplant Surgery, Duke University School of Medicine, Durham, North Carolina.
Weifeng ZengSchool of Medicine and Public Health, Department of Surgery, University of Wisconsin-Madison, Madison, WI.
Isaac AldereteDepartment of Abdominal Transplant Surgery, Duke University School of Medicine, Durham, North Carolina.
Ahmed HassanDepartment of Abdominal Transplant Surgery, Duke University School of Medicine, Durham, North Carolina.
Peter ChlebeckSchool of Medicine and Public Health, Department of Surgery, University of Wisconsin-Madison, Madison, WI.
Kristina MatkowskyjWork completed while at UW-Madison Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI; UW Carbone Cancer Center, University of Wisconsin-Madison, Madison, WI; William S. Middleton Memorial Veterans' Hospital, Department of Pathology, Madison, WI.
Heather JenningsSchool of Medicine and Public Health, Department of Surgery, University of Wisconsin-Madison, Madison, WI.
Andrew S BarbasDepartment of Abdominal Transplant Surgery, Duke University School of Medicine, Durham, North Carolina.
David Al-AdraSchool of Medicine and Public Health, Department of Surgery, University of Wisconsin-Madison, Madison, WI; UW Carbone Cancer Center, University of Wisconsin-Madison, Madison, WI. Electronic address: aladra@wisc.edu.

Funding

Targeting Donor Regulatory Dendritic Cells During Normothermic Ex Vivo Liver Perfusion to Overcome Rejection after Liver TransplantK08AI155816 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI AL-ADRA, DAVID PETER · 2021 to 2025
$894k
NIAID NIH HHS K08 AI155816
6 · The paper itself

Abstract

backgroundRat liver transplant (LT) studies typically utilize the technically demanding orthotopic transplant model, which is stressful for the recipient animal. Therefore, we developed a less technically challenging heterotopic LT model that reduces post-operative animal stress and used this model to characterize rejection in 2 genetically mismatched rat pairs.

methodsSyngeneic transplants were performed with Lewis rats as liver donors and recipients. Allogeneic transplants utilized Dark Agouti donors and Lewis recipients or Lewis donors and Brown Norway recipients. The whole donor liver was transplanted in a heterotopic position in the left side of the abdominal cavity after a left nephrectomy. At pre-defined endpoints, liver grafts were excised and examined using the Banff rejection activity index (RAI).

resultsIn 9 sequential syngeneic transplants there were 2 technical errors that resulted in deaths. The Dark Agouti-Lewis cohort of 7 allogeneic transplants had 1 technical error resulting in death and 2 thrombosis-related graft failures. The Lewis-Brown Norway cohort of 10 transplants had 2 technical errors resulting in death and 3 thrombosis-related graft failures. All technical errors and thrombosis occurred early in each series. Syngeneic transplants demonstrated no rejection (mean RAI of 0). Allogeneic transplants demonstrated mild rejection by post-operative day 3 (mean RAI of 4.5) and severe rejection by post-operative day 8 (mean RAI of 9).

conclusionHeterotopic LT is a viable rejection model that minimizes surgical complexity and animal distress. Allogeneic heterotopic LT demonstrated severe rejection in a timeline similar to the commonly used orthotopic model.

Indexed as

Graft RejectionLiver TransplantationAnimalsDisease Models, AnimalMaleRatsRats, Inbred ACIRats, Inbred BNRats, Inbred LewTransplantation, HeterotopicTransplantation, Homologous

Identifiers

PMID40967922
PMCPMC12495908

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Registered trials

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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.