Evidence map›Paper›PMID 40342868›Full record

ReviewCurrent transplantation reports2025

State of the Art of Bioengineering Approaches in Beta-Cell Replacement.

Jake Miller, Quentin Perrier, Arunkumar Rengaraj, Joshua Bowlby, Lori Byers, Emma Peveri, Wonwoo Jeong, Thomas Ritchey, Alberto Maria Gambelli, Arianna Rossi and 4 more

Abstract readReview
In one paragraph

Review in Current transplantation reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Adenosine as a modulator of human islet function and hypoxic tolerance.Frontiers in bioengineering and biotechnology · 2026
    Article
  3. Review
  4. 3D Bioprinting Strategies in Autoimmune Disease Models.International journal of molecular sciences · 2025
    Review
  5. Review
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

14 authors.

Jake MillerWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Quentin PerrierWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Arunkumar RengarajWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Joshua BowlbyDepartment of Surgery, Atrium Health Wake Forest Baptist, Winston-Salem, NC USA.
Lori ByersWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Emma PeveriWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Wonwoo JeongWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Thomas RitcheyWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Alberto Maria GambelliDepartment of Engineering, University of Perugia, Perugia, Italy.
Arianna RossiDepartment of Engineering, University of Perugia, Perugia, Italy.
Riccardo CalafioreDepartment of Engineering, University of Perugia, Perugia, Italy.
Alice TomeiDiabetes Research Institute, Miller School of Medicine, University of Miami, Miami, FL USA.
Giuseppe OrlandoWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.
Amish AsthanaWake Forest Institute for Regenerative Medicine, Winston-Salem, NC USA.

Funding

A microwell perfusion plate for manufacturing and testing Islet-like clusters.R03DK135460 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ASTHANA, AMISH · 2023 to 2024
$321k
NIDDK NIH HHS R03 DK135460
6 · The paper itself

Abstract

Purpose of the Review: Despite recent advancements in technology for the treatment of type 1 diabetes (T1D), exogenous insulin delivery through automated devices remains the gold standard for treatment. This review will explore progress made in pancreatic islet bioengineering within the field of beta-cell replacement for T1D treatment. Recent Findings: First, we will focus on the use of decellularized extracellular matrices (dECM) as a platform for pancreatic organoid development. These matrices preserve microarchitecture and essential biochemical signals for cell differentiation, offering a promising alternative to synthetic matrices. Second, advancements in 3D bioprinting for creating complex organ structures like pancreatic islets will be discussed. This technology allows for increased precision and customization of cellular models, crucial for replicating native pancreatic islet functionality. Finally, this review will explore the use of stem cell-derived organoids to generate insulin-producing islet-like cells. While these organoids face challenges such as functional immaturity and poor vascularization, they represent a significant advancement for disease modeling, drug screening, and autologous islet transplantation. Summary: These innovative approaches promise to revolutionize T1D treatment by overcoming the limitations of traditional therapies based on human pancreatic islets.

Indexed as

BioengineeringBioprintingExtracellular matrixIslet on a chipIsletsType 1 diabetes

Identifiers

PMID40342868
PMCPMC12055624

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.