Evidence map›Paper›PMID 29165988›Full record

ReviewBioconjugate chemistry2018

Bioconjugate Strategies for the Induction of Antigen-Specific Tolerance in Autoimmune Diseases.

Chunsong Yu, Jingchao Xi, Meng Li, Myunggi An, Haipeng Liu

Abstract readReview
In one paragraph

Review in Bioconjugate chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Multicomponent peptide assemblies.Chemical Society reviews · 2018
    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

5 authors at 1 institution in 1 country.

Chunsong YuDepartment of Chemical Engineering and Materials Science , Wayne State University , Detroit , Michigan 48202 , United States.
Jingchao XiDepartment of Chemical Engineering and Materials Science , Wayne State University , Detroit , Michigan 48202 , United States.
Meng LiDepartment of Chemical Engineering and Materials Science , Wayne State University , Detroit , Michigan 48202 , United States.
Myunggi AnDepartment of Chemical Engineering and Materials Science , Wayne State University , Detroit , Michigan 48202 , United States.
Haipeng LiuDepartment of Chemical Engineering and Materials Science , Wayne State University , Detroit , Michigan 48202 , United States.ORCID 0000-0002-4267-237X
Wayne State University · US

Funding

Design Molecular Vaccines for Type 1 DiabetesR56DK103651 · NIDDK · WAYNE STATE UNIVERSITY · PI LIU, HAIPENG · 2014 to 2015
$476k
NIDDK NIH HHS R56 DK103651
6 · The paper itself

Abstract

Antigen-specific immunotherapy (ASI) holds great promise for the treatment of autoimmune diseases. In mice, administration of major histocompatibility complex (MHC) binding synthetic peptides which modulate T cell receptor (TCR) signaling under subimmunogenic conditions induces selective tolerance without suppressing the global immune responses. However, clinical translation has yielded limited success. It has become apparent that the TCR signaling pathway via synthetic peptide antigen alone is inadequate to induce an effective tolerogenic immunity in autoimmune diseases. Bioconjugate strategies combining additional immunomodulatory functions with TCR signaling can amplify the antigen-specific immune tolerance and possibly lead to the development of new treatments in autoimmune diseases. In this review, we provide a summary of recent advances in the development of bioconjugates to achieve antigen-specific immune tolerance in vivo, with the discussion focused on the underlying design principles and challenges that must be overcome to target these therapies to patients suffering from autoimmune diseases.

Indexed as

Immune ToleranceAnimalsAntigensAutoimmune DiseasesHumansImmunoconjugatesImmunotherapyMajor Histocompatibility ComplexNanoparticlesPeptidesPolymersSmall Molecule LibrariesToll-Like ReceptorsAntigensImmunoconjugatesPeptidesPolymersSmall Molecule LibrariesToll-Like Receptors

Identifiers

PMID29165988
PMCPMC6886668
OpenAlexW2768795880

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.