Evidence map›Paper›PMID 42210983›Full record

ArticleSurgery open science2026

Non-invasive

Chioma Moneme, Antonio Vinicios Alves da Silva, Prisca C Obidike, Bryan A Hogg, Georgia B Brousseau, Casandra Robinson, Christian Roig-Laboy, José Kleybson de Sousa, Yuwen Zhang, Lily S Cheng and 1 more

Abstract read
In one paragraph

Article in Surgery open science, 2026. 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

11 authors.

Chioma MonemeDivision of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, VA, United States of America.
Antonio Vinicios Alves da SilvaDivision of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center and the Department of Pediatrics of the University of Cincinnati College of Medicine, Cincinnati, OH, United States of America.
Prisca C ObidikeDivision of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, VA, United States of America.
Bryan A HoggDivision of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center and the Department of Pediatrics of the University of Cincinnati College of Medicine, Cincinnati, OH, United States of America.
Georgia B BrousseauDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Virginia, United States of America.
Casandra RobinsonDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Virginia, United States of America.
Christian Roig-LaboyDivision of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center and the Department of Pediatrics of the University of Cincinnati College of Medicine, Cincinnati, OH, United States of America.
José Kleybson de SousaDivision of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center and the Department of Pediatrics of the University of Cincinnati College of Medicine, Cincinnati, OH, United States of America.
Yuwen ZhangDivision of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, VA, United States of America.
Lily S ChengDivision of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, VA, United States of America.
Sean R MooreDivision of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center and the Department of Pediatrics of the University of Cincinnati College of Medicine, Cincinnati, OH, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Xenotransplantation of pluripotent stem cell-derived human intestinal organoids (HIOs) into animal hosts models early human small intestinal development. However, traditional methods to assess HIO engraftment and expansion involve invasive, non-survival procedures. We developed a novel HIO platform featuring stable intestinal epithelial expression of a red-shifted luciferase, enabling sensitive, longitudinal Methods: Human embryonic stem cell (hESC) line H9 was lentivirus-transduced with a plasmid encoding red-shifted luciferase under a ubiquitin C promoter. After positive selection, cells were differentiated into endoderm, mid/hindgut spheroids, and HIOs. HIO maturation and luciferase expression were confirmed by immunofluorescence prior to kidney capsule implantation in 10 adult immunodeficient SCID mice. We performed serial Results: Stable transduction did not compromise the genome integrity of hESCs, pluripotency, or maturation of hESCs into HIOs. In 9 of 10 mice, HIO radiance was detectable within two weeks of implantation. Mean radiance significantly increased over time ( Conclusions: We successfully generated transplantable bioluminescent HIOs from pluripotent stem cells, setting the stage for dynamic monitoring of HIOs to further elucidate human intestinal development and injury response across the lifespan and other diverse applications.

Indexed as

Graft survivalHuman intestinal organoids (HIOs)Human pluripotent stem cells (hPSCs)In vivo bioluminescent imagingMouse kidney capsule implantationRed-shifted luciferaseTissue engraftment trackingXenotransplantation, noninvasive longitudinal in vivo monitoring

Identifiers

PMID42210983
PMCPMC13214524

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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.