Evidence map›Paper›PMID 32625203›Full record

ArticleFrontiers in immunology2020

Prediabetes Induced by a Single Autoimmune B Cell Clone.

Nathaniel Phillips, Eugene Ke, Amy Nham, Maximilian Seidl, Brent Freeman, Justin R Abadejos, Changchun Xiao, David Nemazee, Manching Ku, Oktay Kirak

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 4 institutions in 2 countries.

Nathaniel PhillipsDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, United States.
Eugene KeSalk Institute for Biological Studies, La Jolla, CA, United States.
Amy NhamDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, United States.
Maximilian SeidlInstitute of Pathology, Heinrich-Heine University and University Hospital of Düsseldorf, Düsseldorf, Germany.
Brent FreemanDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, United States.
Justin R AbadejosDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, United States.
Changchun XiaoDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, United States.
David NemazeeDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, United States.
Manching KuDivision of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Faculty of Medicine, Medical Center - University of Freiburg, Freiburg, Germany.
Oktay KirakDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, United States.
Scripps Research Institute · USDüsseldorf University Hospital · DESalk Institute for Biological Studies · USUniversity Medical Center Freiburg · DE

Funding

Salk Institute Cancer Training GrantT32CA009370 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Diana Clare Hargreaves, Jan Karlseder · 1986 to 2026
$8.6M
Immune Tolerance in Non-Clonal Immune SystemsR01AI059714 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 2004 to 2013
$3.9M
Immune Tolerance in Non-Clonal Immune SystemsR37AI059714 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 2014 to 2020
$3.5M
NCI NIH HHS T32 CA009370NIAID NIH HHS R01 AI059714NIAID NIH HHS R37 AI059714
6 · The paper itself

Abstract

While B cells play a significant role in the onset of type-1 diabetes (T1D), little is know about their role in those early stages. Thus, to gain new insights into the role of B cells in T1D, we converted a physiological early pancreas-infiltrating B cell into a novel BCR mouse model using Somatic Cell Nuclear Transfer (SCNT). Strikingly, SCNT-derived B1411 model displayed neither developmental block nor anergy. Instead, B1411 underwent spontaneous germinal center reactions. Without T cell help, B1411-Rag1

Indexed as

AutoimmunityAnimalsBasidiomycotaB-LymphocytesCalcium SignalingChromatin Assembly and DisassemblyClone CellsDiabetes Mellitus, ExperimentalFemaleGene Expression ProfilingGlucose Tolerance TestMaleMiceMice, Inbred C57BLMice, Inbred DBAMice, Inbred NODReceptors, Antigen, B-Cellanimal modelautoimmunityB cellcloningdiabetesnucleic acid sensingpancreassomatic cell nuclear transfer (SCNT)

Identifiers

PMID32625203
PMCPMC7314986
OpenAlexW3036285277

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.