Evidence map›Paper›PMID 24556408›Full record

ReviewCurrent opinion in immunology2014

Monitoring peptide processing for MHC class I molecules in the endoplasmic reticulum.

Nilabh Shastri, Niranjana Nagarajan, Kristin C Lind, Takayuki Kanaseki

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  7. ERAPs Reduce In Vitro HIV Infection by Activating Innate Immune Response.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. 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
  14. Review
  15. Review
  16. Review
  17. 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

4 authors at 2 institutions in 2 countries.

Nilabh ShastriDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA. Electronic address: nshastri@berkeley.edu.
Niranjana NagarajanDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Kristin C LindDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Takayuki KanasekiDepartment of Pathology, School of Medicine, Sapporo Medical University, Sapporo, Japan.
University of California, Berkeley · USSapporo Medical University · JP

Funding

Antigen Processing in the Secretory PathwayR37AI060040 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI SADEGH-NASSERI, SCHEHERAZADE · 2012 to 2021
$4.2M
The Endogenous MHC Class I Antigen Processing PathwayR01AI039548 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI SHASTRI, NILABH · 1997 to 2012
$3.8M
GENERATING ANTIGENIC PEPTIDE/MHC BY CRYPTIC TRANSLATIONR01AI044864 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI SHASTRI, NILABH · 2000 to 2010
$2.9M
Antigen processing in the secretory pathwayR01AI060040 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI SHASTRI, NILABH · 2004 to 2010
$2.4M
Immune surveillance via non-classical MHC class Ib moleculesR21AI101751 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI SHASTRI, NILABH · 2012 to 2013
$411k
HLA-peptide repertoire in autoimmunityR21AR063931 · NIAMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI SHASTRI, NILABH · 2013 to 2014
$366k
NIAID NIH HHS R01 AI039548NIAID NIH HHS R01 AI044864NIAID NIH HHS R01 AI060040NIAID NIH HHS R21 AI101751NIAID NIH HHS R37 AI060040NIAMS NIH HHS R21 AR063931
6 · The paper itself

Abstract

Classical MHC class I molecules open a window into the cell by presenting intracellular peptides (pMHC I) on the surface. The peptides are used for immune surveillance by circulating CD8+ T and NK cells to detect and eliminate infected or tumor cells. Not surprisingly, viruses and tumor cells have evolved immune evasion mechanisms to keep the window shades down and the cytotoxic cells oblivious to their presence. Here, we review counter mechanisms that nevertheless allow the immune system to detect and eliminate cells unable to properly process antigenic peptides in the endoplasmic reticulum.

Indexed as

AminopeptidasesAnimalsAntigen PresentationCD8-Positive T-LymphocytesEndoplasmic ReticulumHistocompatibility Antigens Class IHumansKiller Cells, NaturalMiceMinor Histocompatibility AntigensMonitoring, ImmunologicPeptide FragmentsSignal TransductionStem CellsSubstrate SpecificityAminopeptidasesERAP1 protein, humanHistocompatibility Antigens Class IMinor Histocompatibility AntigensPeptide Fragments

Identifiers

PMID24556408
PMCPMC3932006
OpenAlexW2081921422

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.