Evidence map›Paper›PMID 35975353›Full record

ReviewJournal of cellular and molecular medicine2022

Cell delivery systems: Toward the next generation of cell therapies for type 1 diabetes.

Hoang Phuc Dang, Hui Chen, Tim R Dargaville, Bernard E Tuch

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cellular and molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  4. Islet Cell Replacement and Regeneration for Type 1 Diabetes: Current Developments and Future Prospects.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
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  10. Mesenchymal stem cell conditioned medium improves hypoxic injury to protect islet graft function.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Article
  11. Review
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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

4 authors at 3 institutions in 1 country.

Hoang Phuc DangSchool of Life Science, Faculty of Science, University of Technology Sydney, Sydney, New South Wales, Australia.ORCID 0000-0003-1007-2609
Hui ChenSchool of Life Science, Faculty of Science, University of Technology Sydney, Sydney, New South Wales, Australia.ORCID 0000-0001-6883-3752
Tim R DargavilleSchool of Chemistry and Physics, and Centre for Materials Science, Queensland University of Technology, Brisbane, Queensland, Australia.
Bernard E TuchDepartment of Diabetes, Central Clinical School, Faculty of Medicine, Nursing & Health Sciences, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0003-1472-0394
University of Technology Sydney · AUAustralian Cancer Research Foundation · AUQueensland University of Technology · AU

Funding

Additionally, the AFDR has received a research grant from the Juvenile Diabetes Research Foundation to investigate the refinement of a cell delivery system for the treatment of diabetes 1-INO-2-2--914-A-NThe University of Technology Sydney received research funds from the not-for-profit Australian Foundation for Diabetes Research (AFDR), with support from the National Stem Cell Foundation of Australia, to carry out a bioengineered diabetes therapy project using pluripotent stem cells
6 · The paper itself

Abstract

Immunoprotection and oxygen supply are vital in implementing a cell therapy for type 1 diabetes (T1D). Without these features, the transplanted islet cell clusters will be rejected by the host immune system, and necrosis will occur due to hypoxia. The use of anti-rejection drugs can help protect the transplanted cells from the immune system; yet, they also may have severe side effects. Cell delivery systems (CDS) have been developed for islet transplantation to avoid using immunosuppressants. CDS provide physical barriers to reduce the immune response and chemical coatings to reduce host fibrotic reaction. In some CDS, there is architecture to support vascularization, which enhances oxygen exchange. In this review, we discuss the current clinical and preclinical studies using CDS without immunosuppression as a cell therapy for T1D. We find that though CDS have been demonstrated for their ability to support immunoisolation of the grafted cells, their functionality has not been fully optimized. Current advanced methods in clinical trials demonstrate the systems are partly functional, physically complicated to implement or inefficient. However, modifications are being made to overcome these issues.

Indexed as

Diabetes Mellitus, Type 1Islets of LangerhansIslets of Langerhans TransplantationHumansImmunosuppression TherapyOxygenOxygencell delivery systemcell therapyimmunoprotectiontype 1 diabetesvascularization

Identifiers

PMID35975353
PMCPMC9465194
OpenAlexW4292261092

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.