Evidence map›Paper›PMID 28344989›Full record

ArticleMolecular therapy. Methods & clinical development2017

Efficient Presentation of Multiple Endogenous Epitopes to Both CD4

Shamael R Dastagir, Jorge Postigo-Fernandez, Chunliang Xu, James H Stoeckle, Rebuma Firdessa-Fite, Rémi J Creusot

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Antigen-specific immunotherapy with a CD4Nature communications · 2026
    Article
  2. The role of chromogranin A cleavage products in onset of type 1 and 2 diabetes.Frontiers in clinical diabetes and healthcare · 2026
    Review
  3. Review
  4. Epitope-based precision immunotherapy of Type 1 diabetes.Human vaccines & immunotherapeutics · 2023
    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. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
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

6 authors at 1 institution in 1 country.

Shamael R DastagirColumbia Center for Translational Immunology and Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
Jorge Postigo-FernandezColumbia Center for Translational Immunology and Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
Chunliang XuColumbia Center for Translational Immunology and Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
James H StoeckleColumbia Center for Translational Immunology and Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
Rebuma Firdessa-FiteColumbia Center for Translational Immunology and Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
Rémi J CreusotColumbia Center for Translational Immunology and Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.
Columbia University Irving Medical Center · US

Funding

Translational Biomarker Analytical Core (TBAC)P30DK063608 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Rebecca Anne Haeusler, Utpal Pajvani · 2003 to 2026
$36.7M
TRAINING PROGRAM IN ENDOCRINOLOGY AND METABOLISMT32DK007271 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ACCILI, DOMENICO · 1986 to 2019
$6.1M
BD Biosciences InfluxS10OD020056 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SNOECK, HANS-WILLEM E · 2015 to 2015
$600k
NIDDK NIH HHS P30 DK063608NIDDK NIH HHS T32 DK007271
6 · The paper itself

Abstract

Antigen-specific immunotherapy of type 1 diabetes, typically via delivery of a single native β cell antigen, has had little clinical benefit to date. With increasing evidence that diabetogenic T cells react against multiple β cell antigens, including previously unappreciated neo-antigens that can be emulated by mimotopes, a shift from protein- to epitope-based therapy is warranted. To this end, we aimed to achieve efficient co-presentation of multiple major epitopes targeting both CD4

Indexed as

antigen presentationantigen targetingdendritic celldiabetogenicepitopemimotopestromal cellT cellstolerancetype 1 diabetes

Identifiers

PMID28344989
PMCPMC5363322
OpenAlexW2564675412

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.