Evidence map›Paper›PMID 39518902›Full record

ArticleInternational journal of molecular sciences2024

Mucosal Addressin Cell Adhesion Molecule-1 Mediates T Cell Migration into Pancreas-Draining Lymph Nodes for Initiation of the Autoimmune Response in Type 1 Diabetes.

Yankui Li, Rachel C Gunderson, Zeyu Xu, Wenjia Ai, Fanru Shen, Jiayu Ye, Baohui Xu, Sara A Michie

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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
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

0 citing papers in PubMed.

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

8 authors.

Yankui LiDepartment of Vascular Surgery, Tianjin Medical University Second Hospital, Tianjin 300211, China.ORCID 0000-0001-8048-0910
Rachel C GundersonDepartment of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Zeyu XuDepartment of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Wenjia AiDepartment of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-5375-4557
Fanru ShenDepartment of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-4418-4588
Jiayu YeDepartment of Medicine, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Baohui XuDepartment of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-2857-7464
Sara A MichieDepartment of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA.

Funding

NIH HHS DK067592
6 · The paper itself

Abstract

Type 1 diabetes (T1D) is an autoimmune disease that is caused by autoreactive T cell-mediated destruction of insulin-producing β cells in the pancreatic islets. Although naive autoreactive T cells are initially primed by islet antigens in pancreas-draining lymph nodes (pan-LNs), the adhesion molecules that recruit T cells into pan-LNs are unknown. We show that high endothelial venules in pan-LNs of young nonobese diabetic mice have a unique adhesion molecule profile that includes strong expression of mucosal addressin cell adhesion molecule-1 (MAdCAM-1). Anti-MAdCAM-1 antibody blocked more than 80% of the migration of naive autoreactive CD4

Indexed as

Cell Adhesion MoleculesCell MovementDiabetes Mellitus, Type 1Lymph NodesMice, Inbred NODMucoproteinsPancreasAnimalsAutoimmunityCD4-Positive T-LymphocytesMiceCell Adhesion MoleculesMadcam1 protein, mouseMucoproteinsadhesion moleculeregulation T cellsT cell migrationtype 1 diabetes

Identifiers

PMID39518902
PMCPMC11545416

What OpenQuestion holds

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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.