Evidence map›Paper›PMID 23729499›Full record

ArticleJournal of leukocyte biology2013

Regulatory T cell epitopes (Tregitopes) in IgG induce tolerance in vivo and lack immunogenicity per se.

Yan Su, Robert Rossi, Anne S De Groot, David W Scott

Open access · greenAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 38 citations in OpenAlex.

  1. F18 Promiscuous Epitope of Acr1 Protein ofProtein and peptide letters · 2025
    Article
  2. Reproductive Immunology and Pregnancy 2.0.International journal of molecular sciences · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Why Don't We Have a Vaccine Against Autoimmune Diseases? - A Review.Journal of clinical & cellular immunology · 2019
    Article
  10. Review
  11. Article
  12. Inhibitors - cellular aspects and novel approaches for tolerance.Haemophilia : the official journal of the World Federation of Hemophilia · 2014
    Review
  13. Development of Gene Transfer for Induction of Antigen-specific Tolerance.Molecular therapy. Methods & clinical development · 2014
    Article
  14. Review
  15. Review
  16. "Unraveling the Clot-Miscarriage Nexus: Mechanisms, Management, and Future Directions in Thrombosis-Related Recurrent Pregnancy Loss".Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

4 authors at 3 institutions in 1 country.

Yan SuUniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Robert Rossi
Anne S De Groot
David W Scott
Uniformed Services University of the Health Sciences · USProvidence College · USUniversity of Maryland, Baltimore · US

Funding

GENE THERAPEUTIC APPROACH FOR TOLERANCE INDUCTIONR01AI035622 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SCOTT, DAVID WILLIAM · 1997 to 2013
$3.7M
T1D Tolerance Induction with Natural Treg EpitopesR43DK081261 · NIDDK · EPIVAX, INC. · PI DEGROOT, ANNE SEARLS · 2008 to 2009
$600k
NIAID NIH HHS R01 AI035622NIDDK NIH HHS R43 DK081261NIDDK NIH HHS R43DK081261-01
6 · The paper itself

Abstract

Tregitopes are a set of epitopes, derived from IgG, that bind to MHCII, activate nTregs, and promote tolerance. We have now confirmed that coadministration of Tregitopes with a range of proteins (autoantigens and nominal antigens, such as OVA) in vitro and in vivo leads to suppression of T cell and antibody responses to the test antigens. In this study, we demonstrate that Tregitopes are not immunogenic in vivo even when emulsified with strong adjuvants, such as IFA or CFA. Moreover, in vivo administration of Tregitopes with IFA or CFA does not induce Th1 or Th2 cytokine expression under restimulation conditions in vitro. We investigated tolerance induction by codelivering Tregitopes with OVA using B cells. When B cells were pulsed with OVA plus Tregitopes and transferred into naïve mice, we found that cellular and humoral immune responses to the OVA were suppressed. As a result of their ability to induce Tregs and the absence of immunogenicity in the context of strong adjuvants, Tregitopes might be considered a novel immunomodulatory approach for the suppression of immune responses to protein therapeutics (such as FVIII and mAb), as well as for treatment of autoimmune diseases.

Indexed as

Adoptive TransferAnimalsEpitopes, T-LymphocyteForkhead Transcription FactorsImmune ToleranceImmunizationImmunoglobulin GInterferon-gammaIsoantibodiesMiceMice, Inbred BALB CMice, Inbred C57BLOvalbuminPeptide FragmentsT-LymphocytesT-Lymphocytes, RegulatoryEpitopes, T-LymphocyteForkhead Transcription FactorsFoxp3 protein, mouseImmunoglobulin GInterferon-gammaIsoantibodiesOVA 323-339OvalbuminPeptide FragmentsimmunomodulationIVIgTreg

Identifiers

PMID23729499
PMCPMC3714563
OpenAlexW2156659011

What OpenQuestion holds

Textmetadata
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.