Evidence map›Paper›PMID 24214027›Full record

ReviewImmunologic research2013

The IL-2/IL-2R system: from basic science to therapeutic applications to enhance immune regulation.

Allison L Bayer, Alberto Pugliese, Thomas R Malek

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Immunologic research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02772679 (A Phase 1 Trial of CD4+CD127lo/-CD25+ Polyclonal Treg Adoptive Immunotherapy With Interleukin-2 for the Treatment of Type 1 Diabetes), which is not on this map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.3field-weighted citation impact, top 3% 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.

NCT02772679 phase1completednot on this mapstarted 2016, after this paper: background citation

A Phase 1 Trial of CD4+CD127lo/-CD25+ Polyclonal Treg Adoptive Immunotherapy With Interleukin-2 for the Treatment of Type 1 Diabetes

TypeinterventionalSponsorJeffrey BluestoneRan2016 to 2021Enrolled16ConditionsType 1 Diabetes MellitusArmsPolyTregs+IL-2
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 87 citations in OpenAlex.

  1. Hot-Spot-Guided Generative Deep Learning for Drug-Like PPI Inhibitor Design.Interdisciplinary sciences, computational life sciences · 2026
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  19. Dysregulation of T Follicular Helper Cells in Lupus.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Review
  20. 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

3 authors at 1 institution in 1 country.

Allison L BayerDepartment of Microbiology and Immunology, Miller School of Medicine, University of Miami, Miami, FL, 33101, USA.
Alberto Pugliese
Thomas R Malek
University of Miami · US

Funding

Type 1 Diabetes TrialNet Clinical Center: Effects of Alefacept in New Onset T1DU01DK085499 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BAIDAL, DAVID · 2009 to 2018
$4.9M
The immunobiology of CD4+ CD25+ T regulatory cellsR01AI055815 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MALEK, THOMAS R · 2004 to 2015
$3.5M
IL-2-dependent mechanisms in T1DR01DK093866 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MALEK, THOMAS R · 2012 to 2015
$1.3M
Immunomodulation Requirements for Treg Immunotherapy for autoimmune diabetesR56AI101278 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BAYER, ALLISON LORAYNE · 2013 to 2013
$361k
NIAID NIH HHS NIH 1R56AI101278-01A1NIAID NIH HHS NIH R01AI055815NIAID NIH HHS R01 AI055815NIAID NIH HHS R56 AI101278NIDDK NIH HHS NIH 1 U01 DK085499-01NIDDK NIH HHS R01 DK093866NIDDK NIH HHS R01DK093866NIDDK NIH HHS U01 DK085499
6 · The paper itself

Abstract

IL-2 plays a critical role in the normal function of the immune system. A trophic factor for lymphocytes, IL-2 is required for mounting and sustaining adaptive T cell responses; however, IL-2 is also critical for immune regulation via its effects on regulatory T cells (Treg cells). Over the years, we have contributed to the understanding of the biology of IL-2 and its signaling through the IL-2 receptor and helped define the key role played by IL-2 in Treg development and function. Our data show that Treg cells have a heightened sensitivity to IL-2, which may create a therapeutic window to promote immune regulation by selective stimulation of Treg cells. We are now developing new efforts to translate this knowledge to the clinical arena, through our focused interest in Type 1 diabetes as a prototypic autoimmune disease. Specifically, we aim at developing IL-2-based therapeutic regimens and incorporate means to enhance antigen-specific Treg responses, for improved and more selective regulation of islet autoimmunity. In parallel, we are pursuing studies in preclinical models of autoimmunity and transplantation to define critical factors for successful adoptive Treg therapy and develop clinically applicable therapeutic protocols.

Indexed as

Adoptive TransferAnimalsClinical Trials as TopicDiabetes Mellitus, Type 1HomeostasisHumansImmunomodulationImmunotherapyInterleukin-2IsoantigensReceptors, Interleukin-2Signal TransductionT-Lymphocytes, RegulatoryTranslational Research, BiomedicalInterleukin-2IsoantigensReceptors, Interleukin-2

Identifiers

PMID24214027
PMCPMC3990437
OpenAlexW1996128058

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.