Evidence map›Paper›PMID 17457346›Full record

ReviewNature reviews. Immunology2007

Rethinking peptide supply to MHC class I molecules.

Laurence C Eisenlohr, Lan Huang, Tania N Golovina

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Immunology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Article
  2. Article
  3. Kinetically distinct processing pathways diversify the CD8Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  4. Islet stress, degradation and autoimmunity.Diabetes, obesity & metabolism · 2018
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Interaction of TAPBPR, a tapasin homolog, with MHC-I molecules promotes peptide editing.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  11. Article
  12. The nature and extent of contributions by defective ribosome products to the HLA peptidome.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  13. Review
  14. Article
  15. Review
  16. Major source of antigenic peptides for the MHC class I pathway is produced during the pioneer round of mRNA translation.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  17. Review
  18. Article
  19. Article
  20. Cutting Edge: Selective role of ubiquitin in MHC class I antigen presentation.Journal of immunology (Baltimore, Md. : 1950) · 2011
    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

3 authors.

Laurence C EisenlohrLaurence C. Eisenlohr, Lan Huang and Tania N. Golovina are at the Thomas Jefferson University, Jefferson Medical College, Department of Microbiology and Immunology, Philadelphia, Philadelphia 19107, USA.
Lan Huang
Tania N Golovina

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The notion that peptides bound to MHC class I molecules are derived mainly from newly synthesized proteins that are defective, and are therefore targeted for immediate degradation, has gained wide acceptance. This model, still entirely hypothetical, has strong intuitive appeal and is consistent with some experimental results, but it is strained by other findings, as well as by established and emerging concepts in protein quality control. While not discounting defectiveness as a driving force for the processing of some proteins, we propose that MHC-class-I-restricted epitopes are derived mainly from nascent proteins that are accessed by the degradation machinery prior to any assessment of fitness, and we outline one way in which this could be accomplished.

Indexed as

Models, ImmunologicalAnimalsAntigen PresentationHistocompatibility Antigens Class IHumansPeptidesHistocompatibility Antigens Class IPeptides

Identifiers

PMID17457346

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.