Evidence map›Paper›PMID 34326233›Full record

ReviewScience (New York, N.Y.)2021

Strategies for durable β cell replacement in type 1 diabetes.

Todd M Brusko, Holger A Russ, Cherie L Stabler

Open access · greenAbstract readReview
In one paragraph

Review in Science (New York, N.Y.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
17.6field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 120 citations in OpenAlex.

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14 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 1 country.

Todd M BruskoDepartment of Pathology, Immunology and Laboratory Medicine, and Department of Pediatrics, College of Medicine, University of Florida, Gainesville, FL 32610, USA.ORCID 0000-0003-2878-9296
Holger A RussBarbara Davis Center for Diabetes, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0001-5117-2927
Cherie L StablerDepartment of Biomedical Engineering, College of Engineering, University of Florida, Gainesville, FL 32610, USA. cstabler@bme.ufl.edu.ORCID 0000-0003-0573-0646
University of Colorado Anschutz Medical Campus · USUniversity of Florida · USUniversity of Florida Health · US

Funding

Project 3P01AI042288 · NIAID · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 1997 to 2026
$32.9M
University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Maki Nakayama · 2020 to 2026
$10.8M
The CD226 costimulatory axis in type 1 diabetesR01DK106191 · NIDDK · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 2016 to 2026
$4.4M
Engineering a Human Microphysiological System for the Characterization of Islet-Immune InteractionsUH3DK122638 · NIDDK · UNIVERSITY OF FLORIDA · PI AGARWAL, ASHUTOSH, BRUSKO, TODD MICHAEL · 2021 to 2023
$3.0M
Engineering a Human Microphysiological System for the Characterization of Islet-Immune InteractionsUG3DK122638 · NIDDK · UNIVERSITY OF FLORIDA · PI AGARWAL, ASHUTOSH, BRUSKO, TODD MICHAEL · 2019 to 2020
$2.1M
Engineering Immunomodulatory Nanoscale Coatings for Protecting Islet TransplantsR01DK126413 · NIDDK · UNIVERSITY OF FLORIDA · PI STABLER, CHERIE L · 2020 to 2024
$1.7M
Improving human pluripotent stem cell derived beta cell transplantation using genetic lineage tracing.R01DK120444 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI RUSS, HOLGER A. · 2018 to 2021
$1.5M
Stress induced changes to the human beta cell proteomeR21AI140044 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DAVIDSON, HOWARD W, RUSS, HOLGER A. · 2019 to 2020
$428k
NIAID NIH HHS P01 AI042288NIAID NIH HHS R21 AI140044NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK106191NIDDK NIH HHS R01 DK120444NIDDK NIH HHS R01 DK126413NIDDK NIH HHS UG3 DK122638NIDDK NIH HHS UH3 DK122638
6 · The paper itself

Abstract

Technological advancements in blood glucose monitoring and therapeutic insulin administration have improved the quality of life for people with type 1 diabetes. However, these efforts fall short of replicating the exquisite metabolic control provided by native islets. We examine the integrated advancements in islet cell replacement and immunomodulatory therapies that are coalescing to enable the restoration of endogenous glucose regulation. We highlight advances in stem cell biology and graft site design, which offer innovative sources of cellular material and improved engraftment. We also cover cutting-edge approaches for preventing allograft rejection and recurrent autoimmunity. These insights reflect a growing understanding of type 1 diabetes etiology, β cell biology, and biomaterial design, together highlighting therapeutic opportunities to durably replace the β cells destroyed in type 1 diabetes.

Indexed as

ImmunomodulationIslets of Langerhans TransplantationAnimalsAutoimmunityBlood GlucoseCell DifferentiationCell EngineeringCellular MicroenvironmentDiabetes Mellitus, Type 1Graft RejectionGraft SurvivalHumansImmune ToleranceInsulin-Secreting CellsIslets of LangerhansPluripotent Stem CellsBlood Glucose

Identifiers

PMID34326233
PMCPMC8867839
OpenAlexW3185481711

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.