Evidence map›Paper›PMID 30713109›Full record

ArticleCell metabolism2019

A Map of Human Type 1 Diabetes Progression by Imaging Mass Cytometry.

Nicolas Damond, Stefanie Engler, Vito R T Zanotelli, Denis Schapiro, Clive H Wasserfall, Irina Kusmartseva, Harry S Nick, Fabrizio Thorel, Pedro L Herrera, Mark A Atkinson and 1 more

Abstract read
In one paragraph

Article in Cell metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 195 papers.

0numbers the graph read from it
0cells of the map it votes in
195citing 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

195 citing papers in PubMed.

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135 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Nicolas DamondInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Stefanie EnglerInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Vito R T ZanotelliInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland; Systems Biology PhD Program, Life Science Zurich Graduate School, ETH Zurich and University of Zurich, Zurich, Switzerland.
Denis SchapiroInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Clive H WasserfallDepartment of Pathology, Immunology, and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
Irina KusmartsevaDepartment of Pathology, Immunology, and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
Harry S NickDepartment of Neuroscience, College of Medicine, University of Florida, Gainesville, FL, USA.
Fabrizio ThorelDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Pedro L HerreraDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Mark A AtkinsonDepartment of Pathology, Immunology, and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
Bernd BodenmillerInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland. Electronic address: bernd.bodenmiller@imls.uzh.ch.

Funding

Project 3P01AI042288 · NIAID · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 1997 to 2026
$32.9M
Single-Cell Analyses of Human Islets in T1D Using Highly Multiplexed ImagingUC4DK108132 · NIDDK · UNIVERSITY OF FLORIDA · PI ATKINSON, MARK A., BODENMILLER, BERND · 2015 to 2015
$3.6M
NIAID NIH HHS P01 AI042288NIDDK NIH HHS UC4 DK108132
6 · The paper itself

Abstract

Type 1 diabetes (T1D) results from the autoimmune destruction of insulin-producing β cells. A comprehensive picture of the changes during T1D development is lacking due to limited sample availability, inability to sample longitudinally, and the paucity of technologies enabling comprehensive tissue profiling. Here, we analyzed 1,581 islets from 12 human donors, including eight with T1D, using imaging mass cytometry (IMC). IMC enabled simultaneous measurement of 35 biomarkers with single-cell and spatial resolution. We performed pseudotime analysis of islets through T1D progression from snapshot data to reconstruct the evolution of β cell loss and insulitis. Our analyses revealed that β cell destruction is preceded by a β cell marker loss and by recruitment of cytotoxic and helper T cells. The approaches described herein demonstrate the value of IMC for improving our understanding of T1D pathogenesis, and our data lay the foundation for hypothesis generation and follow-on experiments.

Indexed as

BiomarkersDiabetes Mellitus, Type 1Disease ProgressionHumansImage CytometryInsulin-Secreting CellsIslets of LangerhansPancreasBiomarkersendocrine pancreashighly multiplexed imagingimaging mass cytometryimmune cellsin situ imagingislet of LangerhanspseudotimeT cell recruitmenttype 1 diabetesβ cell

Identifiers

PMID30713109
PMCPMC6821395

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.