Evidence map›Paper›PMID 35980300›Full record

ReviewClinical and experimental immunology2022

Clinical and experimental treatment of type 1 diabetes.

S Alice Long, Jane H Buckner

Abstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Integrating Omics into Functional Biomarkers of Type 1 Diabetes.Cold Spring Harbor perspectives in medicine · 2024
    Review
  4. Review
  5. Clinical and Experimental Immunology: highlights from 2022.Clinical and experimental immunology · 2023
    Article
  6. 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

2 authors.

S Alice LongCenter for Translational Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.
Jane H BucknerCenter for Translational Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.ORCID 0000-0002-9005-1885

Funding

Mechanisms of IL-6 mediated T cell pathogenesis in autoimmunityR01AI132774 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI ALTMAN, MATTHEW C., BUCKNER, JANE HOYT · 2017 to 2020
$6.4M
Defining mechanisms of CD8 T cell exhaustion in T1DR01AI141952 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI LONG, S ALICE · 2020 to 2024
$2.8M
NIAID NIH HHS R01 AI132774NIAID NIH HHS R01 AI141952
6 · The paper itself

Abstract

Type 1 diabetes (T1D) is an autoimmune disease resulting in the destruction of the insulin-producing pancreatic beta cells. Disease progression occurs along a trajectory from genetic risk, the development of islet autoantibodies, and autoreactive T cells ultimately progressing to clinical disease. Natural history studies and mechanistic studies linked to clinical trials have provided insight into the role of the immune system in disease pathogenesis. Here, we review our current understanding of the underlying etiology of T1D, focusing on the immune cell types that have been implicated in progression from pre-symptomatic T1D to clinical diagnosis and established disease. This knowledge has been foundational for the development of immunotherapies aimed at the prevention and treatment of T1D.

Indexed as

Autoimmune DiseasesDiabetes Mellitus, Type 1Insulin-Secreting CellsAutoantibodiesAutoimmunityHumansInsulinAutoantibodiesInsulinautoantibodiesautoimmunitycellular immunologydiabetesimmunotherapy

Identifiers

PMID35980300
PMCPMC9750829

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.