Evidence map›Paper›PMID 38993771›Full record

ArticleFrontiers in transplantation2024

Development of a large animal orthotopic intestinal transplantation model with long-term survival for study of immunologic outcomes.

Sarah Merl, Bryan Chen, M Esad Gunes, Hussein Atta, Kryscilla Yang, Dilrukshi Ekanayake-Alper, Dominik Hajosi, Fei Huang, Brittany Bhola, Satyajit Patwardhan and 7 more

Abstract read
In one paragraph

Article in Frontiers in transplantation, 2024. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

17 authors.

Sarah MerlColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Bryan ChenColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
M Esad GunesColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Hussein AttaColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Kryscilla YangColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Dilrukshi Ekanayake-AlperColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Dominik HajosiColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Fei HuangColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Brittany BholaColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Satyajit PatwardhanColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Philip JordacheColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Greg NowakColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Mercedes MartinezColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Tomoaki KatoColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Megan SykesColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Kazuhiko YamadaColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.
Joshua WeinerColumbia Center for Translational Immunology, Columbia University, New York, NY, United States.

Funding

Defining the relationship between host-microbiome interactions and rejection after intestinal transplantationK23AI156026 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WEINER, JOSHUA · 2021 to 2025
$962k
NIAID NIH HHS K23 AI156026
6 · The paper itself

Abstract

Introduction: Intestinal transplantation (ITx) is the last remaining therapy for patients with intestinal failure once parenteral nutrition is no longer an option, however its use is limited by immunological complications, including high rates of rejection and morbidity associated with immunosuppression, such as infection and malignancy. We aimed to develop a large animal model of ITx with which to study the immune response to ITx and to design and test tolerance induction regimens. Methods: Learning from prior complications, we developed and progressively improved both surgical methods for the donor and recipient as well as postoperative management strategies. Methods of stoma generation, bowel positioning, vessel preparation, and fluid management were optimized. The immunosuppression strategy mirrored our clinical regimen. Results: As a result of our modifications, results improved from survival less than 1 month to consistent long-term survival with good graft function. We review several techniques that were developed to avoid pitfalls that were encountered, which can be used to optimize outcomes in this model. Discussion: Achieving long-term survival after swine orthotopic ITx permits immunological analysis and pre-clinical trials in a large animal model of ITx.

Indexed as

intestinemodelorthotopicswinetransplant

Identifiers

PMID38993771
PMCPMC11235311

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.