Evidence map›Paper›PMID 35393479›Full record

ArticleScientific reports2022

Syngeneically transplanted insulin producing cells differentiated from adipose derived stem cells undergo delayed damage by autoimmune responses in NOD mice.

Kazunori Tokuda, Tetsuya Ikemoto, Shoko Yamashita, Katsuki Miyazaki, Shohei Okikawa, Shinichiro Yamada, Yu Saito, Yuji Morine, Mitsuo Shimada

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

9 authors at 1 institution in 1 country.

Kazunori TokudaDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Tetsuya IkemotoDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan. ikemoto.tetsuya@tokushima-u.ac.jp.
Shoko YamashitaDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Katsuki MiyazakiDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Shohei OkikawaDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Shinichiro YamadaDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Yu SaitoDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Yuji MorineDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Mitsuo ShimadaDepartment of Digestive and Transplant Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Tokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin-producing cells (IPCs) generated by our established protocol have reached the non-clinical 'proof of concept' stage. Our strategy for their clinical application is the autotransplantation of IPCs into patients with type 1 diabetes mellitus (T1DM). In this context, the autoimmunity that characterized T1DM is important, rather than allorejection. We aimed to determine how these IPCs respond to T1DM autoimmunity. IPCs were generated from the subcutaneous fat tissue of non-obese diabetic (NOD) mice using our protocol. IPCs derived from NOD mice were transplanted under the kidney capsules of NOD mice at the onset of diabetes and the subsequent changes in blood glucose concentration were characterized. Blood glucose decreased within 30 days of transplantation, but increased again after 40-60 days in three of four recipient NOD mice. In tissue samples, the numbers of CD4

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Insulin-Secreting CellsAnimalsAutoimmunityBlood GlucoseCD8-Positive T-LymphocytesHumansInsulinMiceMice, Inbred NODStem CellsBlood GlucoseInsulin

Identifiers

PMID35393479
PMCPMC8991208
OpenAlexW4223656301

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.