Evidence map›Paper›PMID 35533022›Full record

ArticleJournal of diabetes investigation2022

Combination of anti-CD25 antibody and poly I:C treatment in pregnant NOD mice may be used as 'pregnancy-related' type 1 diabetes model.

Akira Shimada, Kyoko Toda, Ikuo Inoue, Taketo Yamada, Yoichi Oikawa

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 94% 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

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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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 1 institution in 1 country.

Akira ShimadaDepartment of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.ORCID https://orcid.org/0000-0002-3954-4983
Kyoko TodaDepartment of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Ikuo InoueDepartment of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Taketo YamadaDepartment of Pathology, Saitama Medical University, Saitama, Japan.
Yoichi OikawaDepartment of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.ORCID https://orcid.org/0000-0003-1524-6751
Saitama Medical University · JP

Funding

Saitama Medical University
6 · The paper itself

Abstract

AIMS/

introductionSome women develop type 1 diabetes during pregnancy or immediately after delivery. However, the underlying pathophysiology remains largely unknown, probably because of the lack of a suitable animal model. In this study, we administered pregnant NOD mice with an anti-CD25 antibody to reduce regulatory T cells along with poly I:C and examined the onset of diabetes. MATERIALS AND

methodsAnti-CD25 antibody and poly I:C were intraperitoneally administered to mated female NOD mice. Mice delivered within 3 weeks after the treatment, and the onset of diabetes during pregnancy or within 6 weeks after delivery was examined. Some mice were killed 1 week after treatment, and their spleen and pancreas were excised to examine the expression levels of cytokines and for histological examination.

resultsHalf of the mice treated with anti-CD25 antibody plus poly I:C developed diabetes, as compared with none of the poly I:C-injected mice (P < 0.05). The ratios of interleukin-18/forkhead box P3 and granzyme B/forkhead box P3 were higher in the pancreas of anti-CD25 antibody plus poly I:C-treated mice than in the pancreas of control mice. The insulitis score decreased in the pancreas of anti-CD25 antibody plus poly I:C-injected pregnant NOD mice.

conclusionsWe describe the use of anti-CD25 antibody to reduce regulatory T cells and poly I:C as a Toll-like receptor 3 stimulator to mimic viral infection in a pregnant NOD mouse, which can be used as a model of 'pregnancy-related' type 1 diabetes.

Indexed as

Diabetes Mellitus, Type 1AnimalsFemaleHumansMiceMice, Inbred NODPancreasPoly IPregnancyT-Lymphocytes, RegulatoryPoly INOD mousePregnancyType 1 diabetes

Identifiers

PMID35533022
PMCPMC9434566
OpenAlexW4229444418

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.