Evidence map›Paper›PMID 35308825›Full record

ArticleFrontiers in bioengineering and biotechnology2021

Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice.

Adam M Syanda, Vera I Kringstad, Samuel J I Blackford, Joachim S Kjesbu, Soon Seng Ng, Liang Ma, Fang Xiao, Abba E Coron, Anne Mari A Rokstad, Sunil Modi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 16 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 2 institutions in 2 countries.

Adam M SyandaDepartment of Metabolism, Digestion and Reproduction, Imperial College London (ICL), London, United Kingdom.
Vera I KringstadDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Samuel J I BlackfordDepartment of Metabolism, Digestion and Reproduction, Imperial College London (ICL), London, United Kingdom.
Joachim S KjesbuDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Soon Seng NgDepartment of Metabolism, Digestion and Reproduction, Imperial College London (ICL), London, United Kingdom.
Liang MaDepartment of Metabolism, Digestion and Reproduction, Imperial College London (ICL), London, United Kingdom.
Fang XiaoDepartment of Metabolism, Digestion and Reproduction, Imperial College London (ICL), London, United Kingdom.
Abba E CoronDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Anne Mari A RokstadDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Sunil ModiDepartment of Metabolism, Digestion and Reproduction, Imperial College London (ICL), London, United Kingdom.
S Tamir RashidDepartment of Metabolism, Digestion and Reproduction, Imperial College London (ICL), London, United Kingdom.
Berit Løkensgard StrandDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Imperial College London · GBNorwegian University of Science and Technology · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intra-peritoneal placement of alginate encapsulated human induced pluripotent stem cell-derived hepatocytes (hPSC-Heps) represents a potential new bridging therapy for acute liver failure. One of the rate-limiting steps that needs to be overcome to make such a procedure more efficacious and safer is to reduce the accumulation of fibrotic tissue around the encapsulated cells to allow the free passage of relevant molecules in and out for metabolism. Novel chemical compositions of alginate afford the possibility of achieving this aim. We accordingly used sulfated alginate and demonstrated that this material reduced fibrotic overgrowth whilst not impeding the process of encapsulation nor cell function. Cumulatively, this suggests sulfated alginate could be a more suitable material to encapsulate hPSC-hepatocyte prior to human use.

Indexed as

acute liver failurecGMPhPSCimmunogenicityimmunoisolationPFOpluripotent stem cell-derived hepatocytessulfated alginate

Identifiers

PMID35308825
PMCPMC8928731
OpenAlexW4214844052

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.