Evidence map›Paper›PMID 21844706›Full record

ReviewCurrent opinion in endocrinology, diabetes, and obesity2011

2011 Update: antigen-specific therapy in type 1 diabetes.

Aaron W Michels, Matthias von Herrath

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in endocrinology, diabetes, and obesity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Type 1 diabetes: A predictable disease.World journal of diabetes · 2015
    Review
  11. Article
  12. Review
  13. Article
  14. Targeting the trimolecular complex.Clinical immunology (Orlando, Fla.) · 2013
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. [Update on type 1 diabetes].Der Internist · 2013
    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 at 2 institutions in 1 country.

Aaron W MichelsBarbara Davis Center for Childhood Diabetes, University of Colorado Denver, Aurora, Colorado 80045, USA. Aaron.Michels@ucdenver.edu
Matthias von Herrath
La Jolla Institute for Immunology · USUniversity of Colorado Denver · US

Funding

Small Molecules Targeting Allele Specific MHC Class II PresentationK08DK095995 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MICHELS, AARON W · 2012 to 2016
$762k
NIDDK NIH HHS K08 DK095995PHS HHS U01
6 · The paper itself

Abstract

purpose of reviewTo update on the clinical trials using antigen-specific therapies in autoimmune diabetes. RECENT

findingsType 1 diabetes is now a predictable disease with the measurement of islet autoantibodies, and the incidence is increasing dramatically. Well tolerated and effective interventions are needed to stop the underlying autoimmune destruction of insulin-producing beta cells. Beta-cell antigens, insulin and glutamic acid decarboxylase, are being used to preserve endogenous insulin production in individuals with new-onset diabetes and to prevent diabetes. The results of antigen-specific immune intervention trials are reviewed and consideration is given to future directions for inducing tolerance in type 1 diabetes. SUMMARY: Antigen-specific immune therapies act by enhancing regulatory T cell function, in animal models often locally and selectively in islets or pancreatic lymph nodes while inhibiting effector T cells. This therapeutic pathway provides a safe treatment to preserve beta cell function in new-onset diabetic individuals with the GAD-Alum vaccine being the most extensively studied therapy. Insulin is being used in many forms to prevent diabetes and stop the underlying autoimmune process. For the future, combination immune therapies targeting different pathways in the immune system will be needed to effectively induce sustained tolerance in type 1 diabetes.

Indexed as

Alum CompoundsAnimalsAntigensClinical Trials as TopicDiabetes Mellitus, Type 1Glutamate DecarboxylaseHumansHypoglycemic AgentsImmunotherapyInsulinVaccinesAlum CompoundsAntigensGlutamate DecarboxylaseHypoglycemic AgentsInsulinVaccines

Identifiers

PMID21844706
PMCPMC4016762
OpenAlexW2075745554

What OpenQuestion holds

Textmetadata
LicenceTDM
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.