Evidence map›Paper›PMID 23576302›Full record

ArticleEuropean journal of immunology2013

Partial MHC class II constructs inhibit MIF/CD74 binding and downstream effects.

Gil Benedek, Roberto Meza-Romero, Shayne Andrew, Lin Leng, Gregory G Burrows, Dennis Bourdette, Halina Offner, Richard Bucala, Arthur A Vandenbark

Abstract read
In one paragraph

Article in European journal of immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

41 citing papers in PubMed, 53 citations in OpenAlex.

  1. MIF Tautomerase Inhibition Protects Neurons From Immune-Mediated Cell Death.Neurology(R) neuroimmunology & neuroinflammation · 2026
    Article
  2. Article
  3. MIF contribution to progressive brain diseases.Journal of neuroinflammation · 2024
    Review
  4. Article
  5. Article
  6. Therapy targeting antigen-specific T cells by a peptide-based tolerizing vaccine against autoimmune arthritis.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
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  13. Article
  14. Review
  15. Article
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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

9 authors at 3 institutions in 1 country.

Gil BenedekDepartment of Veterans Affairs Medical Center, Neuroimmunology Research, Portland, OR 97239, USA.
Roberto Meza-Romero
Shayne Andrew
Lin Leng
Gregory G Burrows
Dennis Bourdette
Halina Offner
Richard Bucala
Arthur A Vandenbark
Oregon Health & Science University · USYale University · USPortland VA Medical Center · US

Funding

Mechanisms of Rheumatoid Synovial Fibroblast ActivationR01AR049610 · NIAMS · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2002 to 2018
$5.0M
INNATE AND ADAPTIVE MECHANISMS IN ARTHRITISR01AR050498 · NIAMS · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2004 to 2013
$3.6M
REGULATION OF EAE WITH RECOMBINANT TCR LIGANDSR01NS047661 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI VANDENBARK, ARTHUR A. · 2005 to 2014
$3.2M
NIAMS NIH HHS AR050498NIAMS NIH HHS R01 AR049610NIAMS NIH HHS R01 AR050498NINDS NIH HHS NS47661NINDS NIH HHS R01 NS047661
6 · The paper itself

Abstract

MIF and its receptor, CD74, are pivotal regulators of the immune system. Here, we demonstrate for the first time that partial MHC class II constructs comprised of linked β1α1 domains with covalently attached antigenic peptides (also referred to as recombinant T-cell receptor ligands - RTLs) can inhibit MIF activity by not only blocking the binding of rhMIF to immunopurified CD74, but also downregulating CD74 cell-surface expression. This bifunctional inhibition of MIF/CD74 interactions blocked downstream MIF effects, including enhanced secretion of proinflammatory cytokines, anti-apoptotic activity, and inhibition of random migration that all contribute to the reversal of clinical and histological signs of EAE. Moreover, we demonstrate that enhanced CD74 cell-surface expression on monocytes in mice with EAE and subjects with multiple sclerosis can be downregulated by humanized RTLs, resulting in reduced MIF binding to the cells. Thus, binding of partial MHC complexes to CD74 blocks both the accessibility and availability of CD74 for MIF binding and downstream inflammatory activity.

Indexed as

AnimalsAntigens, Differentiation, B-LymphocyteCell MovementCytokinesEncephalomyelitis, Autoimmune, ExperimentalGene Expression RegulationHistocompatibility Antigens Class IIHumansIntramolecular OxidoreductasesLigandsMacrophage Migration-Inhibitory FactorsMiceMultiple SclerosisPeptidesProtein BindingProtein Structure, TertiaryAntigens, Differentiation, B-LymphocyteCytokinesHistocompatibility Antigens Class IIIntramolecular Oxidoreductasesinvariant chainLigandsMacrophage Migration-Inhibitory FactorsMIF protein, humanMif protein, mousePeptidesReceptors, Antigen, T-CellRecombinant Proteins

Identifiers

PMID23576302
PMCPMC3788583
OpenAlexW1485720010

What OpenQuestion holds

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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.