Evidence map›Paper›PMID 26863343›Full record

ArticleJournal of visualized experiments : JoVE2016

A Novel Microsurgical Model for Heterotopic, En Bloc Chest Wall, Thymus, and Heart Transplantation in Mice.

Byoungchol Oh, Georg J Furtmüller, Michael Sosin, Madeline L Fryer, Lawrence J Gottlieb, Michael R Christy, Gerald Brandacher, Amir H Dorafshar

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Efficacy of single-agent immunosuppressive regimens in a murine model of vascularized composite allotransplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2020
    Article
  2. Article
  3. Murine Full-thickness Skin Transplantation.Journal of visualized experiments : JoVE · 2017
    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

8 authors at 3 institutions in 1 country.

Byoungchol OhJohns Hopkins University School of Medicine.
Georg J FurtmüllerJohns Hopkins University School of Medicine.
Michael SosinJohns Hopkins University School of Medicine.
Madeline L FryerJohns Hopkins University School of Medicine.
Lawrence J GottliebBurn and Complex Wound Center; Section of Plastic and Reconstructive Surgery, University of Chicago Medical Center.
Michael R ChristyDivision of Plastic, Reconstructive, and Maxillofacial Surgery, R Adams Cowley Shock Trauma Center.
Gerald BrandacherJohns Hopkins University School of Medicine; Department of Plastic and Reconstructive Surgery, Johns Hopkins University School of Medicine; Vascularized Composite Allotransplantation (VCA) Lab, Johns Hopkins University School of Medicine; gbranda2@jhmi.edu.
Amir H DorafsharJohns Hopkins University School of Medicine; Department of Plastic and Reconstructive Surgery, Johns Hopkins University School of Medicine; Vascularized Composite Allotransplantation (VCA) Lab, Johns Hopkins University School of Medicine; adorafs1@jhmi.edu.
Johns Hopkins Medicine · USJohns Hopkins University · USWound Healing Society · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exploration of novel strategies in organ transplantation to prolong allograft survival and minimizing the need for long-term maintenance immunosuppression must be pursued. Employing vascularized bone marrow transplantation and co-transplantation of the thymus have shown promise in this regard in various animal models. Vascularized bone marrow transplantation allows for the uninterrupted transfer of donor bone marrow cells within the preserved donor microenvironment, and the incorporation of thymus tissue with vascularized bone marrow transplantation has shown to increase T-cell chimerism ultimately playing a supportive role in the induction of immune regulation. The combination of solid organ and vascularized composite allotransplantation can uniquely combine these strategies in the form of a novel transplant model. Murine models serve as an excellent paradigm to explore the mechanisms of acute and chronic rejection, chimerism, and tolerance induction, thus providing the foundation to propagate superior allograft survival strategies for larger animal models and future clinical application. Herein, we developed a novel heterotopic en bloc chest wall, thymus, and heart transplant model in mice using a cervical non-suture cuff technique. The experience in syngeneic and allogeneic transplant settings is described for future broader immunological investigations via an instructional manuscript and video supplement.

Indexed as

Models, AnimalAnimalsGraft SurvivalHeart TransplantationMiceThoracic WallThymus GlandTransplantation, Homologous

Identifiers

PMID26863343
PMCPMC4781677
OpenAlexW2260861971

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.