Evidence map›Paper›PMID 22138314›Full record

ReviewCurrent opinion in immunology2012

The mechanism of HLA-DM induced peptide exchange in the MHC class II antigen presentation pathway.

Monika-Sarah E D Schulze, Kai W Wucherpfennig

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2012. 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
3.3field-weighted citation impact, top 7% 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, 73 citations in OpenAlex.

  1. Technical review of artificial intelligence in TCR-T therapy.Journal of the National Cancer Center · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Structural insights into human MHC-II association with invariant chain.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Review
  10. Article
  11. Review
  12. Role of B cells as antigen presenting cells.Frontiers in immunology · 2022
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Successive crystal structure snapshots suggest the basis for MHC class I peptide loading and editing by tapasin.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Review
  20. Article
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

2 authors at 2 institutions in 2 countries.

Monika-Sarah E D SchulzeDepartment of Cancer Immunology & AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Kai W Wucherpfennig
Dana-Farber Cancer Institute · USHarvard University · US

Funding

TCR recognition of MHC class II peptide compexes in multiple sclerosisP01AI045757 · NIAID · DANA-FARBER CANCER INSTITUTE · PI WUCHERPFENNIG, KAI W · 1999 to 2017
$22.8M
Structural Determinants of TCR Assembly and SignalingR01AI054520 · NIAID · DANA-FARBER CANCER INSTITUTE · PI WUCHERPFENNIG, KAI W · 2003 to 2013
$4.0M
Inhibition of Antigen Presentation in Multiple SclerosisR01NS044914 · NINDS · DANA-FARBER CANCER INSTITUTE · PI WUCHERPFENNIG, KAI W · 2003 to 2012
$3.2M
Mechanisms of Antigen Presentation by MHC class IIR01AI057493 · NIAID · DANA-FARBER CANCER INSTITUTE · PI WUCHERPFENNIG, KAI W · 2004 to 2008
$1.9M
NIAID NIH HHS P01 AI045757NIAID NIH HHS R01 AI054520NIAID NIH HHS R01 AI057493NINDS NIH HHS R01 NS044914
6 · The paper itself

Abstract

HLA-DM serves a critical function in the loading and editing of peptides on MHC class II (MHCII) molecules. Recent data showed that the interaction cycle between MHCII molecules and HLA-DM is dependent on the occupancy state of the peptide binding groove. Empty MHCII molecules form stable complexes with HLA-DM, which are disrupted by binding of high-affinity peptide. Interestingly, MHCII molecules with fully engaged peptides cannot interact with HLA-DM, and prior dissociation of the peptide N-terminus from the groove is required for HLA-DM binding. There are significant similarities to the peptide loading process for MHC class I molecules, even though it is executed by a distinct set of proteins in a different cellular compartment.

Indexed as

AnimalsAntigen PresentationHistocompatibility Antigens Class IIHLA-D AntigensHumansPeptidesH2-M antigensHistocompatibility Antigens Class IIHLA-D AntigensHLA-DM antigensPeptides

Identifiers

PMID22138314
PMCPMC3288754
OpenAlexW1989011018

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.