Evidence mapPaperPMID 38100042Full record

ArticleEJNMMI research2023

Preclinical evaluation of Affibody molecule for PET imaging of human pancreatic islets derived from stem cells.

Pierre Cheung, Julia Thorngren, Bo Zhang, Svitlana Vasylovska, Francesco Lechi, Jonas Persson, Stefan Ståhl, John Löfblom, Olle Korsgren, Jonas Eriksson and 2 more

Open access · goldAbstract read
In one paragraph

Article in EJNMMI research, 2023. 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
2.2field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Pierre Cheung *Science for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
Julia Thorngren *Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Bo ZhangScience for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
Svitlana VasylovskaDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Francesco LechiScience for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
Jonas PerssonDepartment of Protein Science, Division of Protein Engineering, KTH Royal Institute of Technology, Stockholm, Sweden.
Stefan StåhlDepartment of Protein Science, Division of Protein Engineering, KTH Royal Institute of Technology, Stockholm, Sweden.
John LöfblomDepartment of Protein Science, Division of Protein Engineering, KTH Royal Institute of Technology, Stockholm, Sweden.
Olle KorsgrenDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Jonas ErikssonScience for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
Joey Lau *Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden. joey.lau@mcb.uu.se.
Olof Eriksson *Science for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden. olof.eriksson@ilk.uu.se.
Uppsala University · SEKTH Royal Institute of Technology · SEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBeta-cell replacement methods such as transplantation of isolated donor islets have been proposed as a curative treatment of type 1 diabetes, but widespread application is challenging due to shortages of donor tissue and the need for continuous immunosuppressive treatments. Stem-cell-derived islets have been suggested as an alternative source of beta cells, but face transplantation protocols optimization difficulties, mainly due to a lack of available methods and markers to directly monitor grafts survival, as well as their localization and function. Molecular imaging techniques and particularly positron emission tomography has been suggested as a tool for monitoring the fate of islets after clinical transplantation. The integral membrane protein DGCR2 has been demonstrated to be a potential pancreatic islet biomarker, with specific expression on insulin-positive human embryonic stem-cell-derived pancreatic progenitor cells. The candidate Affibody molecule Z

results[

conclusionTargeting of DGCR2 is a promising approach for in vivo detection of stem-cell-derived islets grafts by molecular imaging. The synthesis of [

Indexed as

Affibody moleculeDGCR2DiabetesFluorine-18 chemistryPETStem cells

Identifiers

PMID38100042
PMCPMC10724103
OpenAlexW4389801652

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.