Evidence map›Paper›PMID 33671312›Full record

ReviewBiomedicines2021

Non-Genetically Encoded Epitopes Are Relevant Targets in Autoimmune Diabetes.

Hai Nguyen, Perrin Guyer, Ruth A Ettinger, Eddie A James

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Preclinical evaluation of a precision medicine approach to DNA vaccination in type 1 diabetes.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Article
  7. 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

4 authors at 1 institution.

Hai NguyenTranslational Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA 98101, USA.
Perrin GuyerTranslational Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA 98101, USA.
Ruth A EttingerTranslational Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA 98101, USA.
Eddie A JamesTranslational Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA 98101, USA.ORCID 0000-0002-7217-5729
Benaroya Research Institute

Funding

Juvenile Diabetes Research Foundation United States of America 1-SRA-2020-978-S-B
6 · The paper itself

Abstract

Islet antigen reactive T cells play a key role in promoting beta cell destruction in type 1 diabetes (T1D). Self-reactive T cells are typically deleted through negative selection in the thymus or deviated to a regulatory phenotype. Nevertheless, those processes are imperfect such that even healthy individuals have a reservoir of potentially autoreactive T cells. What remains less clear is how tolerance is lost to insulin and other beta cell specific antigens. Islet autoantibodies, the best predictor of disease risk, are known to recognize classical antigens such as proinsulin, GAD65, IA-2, and ZnT8. These antibodies are thought to be supported by the expansion of autoreactive CD4

Indexed as

neo-antigenpost-translational modificationselectionT celltype 1 diabetes

Identifiers

PMID33671312
PMCPMC7922826
OpenAlexW3129992452

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.