Evidence map›Paper›PMID 38360355›Full record

ReviewAdvanced drug delivery reviews2024

Encapsulation and immune protection for type 1 diabetes cell therapy.

Sophia Kioulaphides, Andrés J García

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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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

2 authors.

Sophia KioulaphidesWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA 30332, USA.
Andrés J GarcíaGeorge W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA. Electronic address: andres.garcia@me.gatech.edu.

Funding

Hydrogels for human beta cell survival, function and evasion of immune rejectionR01DK133702 · NIDDK · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J, LEI, JI · 2022 to 2025
$3.3M
BIOMATERIALS FOR STEM CELL-DERIVED BETA CELL TRANSPLANTATIONR01DK128840 · NIDDK · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J, SHIRWAN, HAVAL · 2021 to 2025
$2.1M
NIDDK NIH HHS R01 DK128840NIDDK NIH HHS R01 DK133702
6 · The paper itself

Abstract

Type 1 Diabetes (T1D) involves the autoimmune destruction of insulin-producing β-cells in the pancreas. Exogenous insulin injections are the current therapy but are user-dependent and cannot fully recapitulate physiological insulin secretion dynamics. Since the emergence of allogeneic cell therapy for T1D, the Edmonton Protocol has been the most promising immunosuppression protocol for cadaveric islet transplantation, but the lack of donor islets, poor cell engraftment, and required chronic immunosuppression have limited its application as a therapy for T1D. Encapsulation in biomaterials on the nano-, micro-, and macro-scale offers the potential to integrate islets with the host and protect them from immune responses. This method can be applied to different cell types, including cadaveric, porcine, and stem cell-derived islets, mitigating the issue of a lack of donor cells. This review covers progress in the efforts to integrate insulin-producing cells from multiple sources to T1D patients as a form of cell therapy.

Indexed as

Diabetes Mellitus, Type 1Islets of LangerhansIslets of Langerhans TransplantationAnimalsCadaverHumansInsulinSwineInsulinBiomaterialsCadaveric isletsImmune responsePorcine isletsStem cell-derived β-cells

Identifiers

PMID38360355
PMCPMC10948298

What OpenQuestion 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 OpenQuestion graph.