Evidence map›Paper›PMID 30853374›Full record

ArticleStem cell reports2019

Macroencapsulated Human iPSC-Derived Pancreatic Progenitors Protect against STZ-Induced Hyperglycemia in Mice.

Corinne Haller, Julie Piccand, Filippo De Franceschi, Yuki Ohi, Anindita Bhoumik, Christophe Boss, Umberto De Marchi, Guillaume Jacot, Sylviane Metairon, Patrick Descombes and 6 more

Abstract read
In one paragraph

Article in Stem cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

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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

16 authors.

Corinne HallerNestlé Research, Nestlé Institute of Health Sciences, Stem Cells Unit, EPFL Innovation Park, Building G, 1015 Lausanne, Switzerland.
Julie PiccandNestlé Research, Nestlé Institute of Health Sciences, Stem Cells Unit, EPFL Innovation Park, Building G, 1015 Lausanne, Switzerland.
Filippo De FranceschiNestlé Research, Nestlé Institute of Health Sciences, Department of Flow Cytometry, Lausanne, Switzerland.
Yuki OhiViaCyte, San Diego, CA, USA.
Anindita BhoumikViaCyte, San Diego, CA, USA.
Christophe BossNestlé Research, Nestlé Institute of Health Sciences, Department of Device Engineering, Lausanne, Switzerland.
Umberto De MarchiNestlé Research, Nestlé Institute of Health Sciences, Department of Mitochondrial Function, Lausanne, Switzerland.
Guillaume JacotNestlé Research, Nestlé Institute of Health Sciences, Department of Natural Bioactive and Screening, Lausanne, Switzerland.
Sylviane MetaironNestlé Research, Nestlé Institute of Health Sciences, Department of Functional Genomics, Lausanne, Switzerland.
Patrick DescombesNestlé Research, Nestlé Institute of Health Sciences, Department of Functional Genomics, Lausanne, Switzerland.
Andreas WiederkehrNestlé Research, Nestlé Institute of Health Sciences, Department of Mitochondrial Function, Lausanne, Switzerland.
Alessio PaliniNestlé Research, Nestlé Institute of Health Sciences, Department of Flow Cytometry, Lausanne, Switzerland.
Nicolas BoucheNestlé Research, Nestlé Institute of Health Sciences, Department of Device Engineering, Lausanne, Switzerland.
Pascal SteinerNestlé Research, Nestlé Institute of Health Sciences, Department of Brain Health, Lausanne, Switzerland.
Olivia G KellyViaCyte, San Diego, CA, USA.
Marine R-C KrausNestlé Research, Nestlé Institute of Health Sciences, Stem Cells Unit, EPFL Innovation Park, Building G, 1015 Lausanne, Switzerland. Electronic address: marine.kraus@rd.nestle.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In type 1 diabetes, a renewable source of human pancreatic β cells, in particular from human induced pluripotent stem cell (hiPSC) origin, would greatly benefit cell therapy. Earlier work showed that pancreatic progenitors differentiated from human embryonic stem cells in vitro can further mature to become glucose responsive following macroencapsulation and transplantation in mice. Here we took a similar approach optimizing the generation of pancreatic progenitors from hiPSCs. This work demonstrates that hiPSCs differentiated to pancreatic endoderm in vitro can be efficiently and robustly generated under large-scale conditions. The hiPSC-derived pancreatic endoderm cells (HiPECs) can further differentiate into glucose-responsive islet-like cells following macroencapsulation and in vivo implantation. The HiPECs can protect mice from streptozotocin-induced hyperglycemia and maintain normal glucose homeostasis and equilibrated plasma glucose concentrations at levels similar to the human set point. These results further validate the potential use of hiPSC-derived islet cells for application in clinical settings.

Indexed as

Stem Cell TransplantationAnimalsBiomarkersBlood GlucoseCell DifferentiationC-PeptideDiabetes Mellitus, ExperimentalDisease Models, AnimalEndodermFluorescent Antibody TechniqueHumansHyperglycemiaImmunophenotypingInduced Pluripotent Stem CellsInsulinInsulin-Secreting CellsBiomarkersBlood GlucoseC-PeptideInsulindiabetes mellitusdifferentiationencapsulationhumaniPSCstem celltherapyβ cell

Identifiers

PMID30853374
PMCPMC6449839

What OpenQuestion holds

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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.