Evidence map›Paper›PMID 22522492›Full record

ArticleNature immunology2012

Nonclassical MHC class Ib-restricted cytotoxic T cells monitor antigen processing in the endoplasmic reticulum.

Niranjana A Nagarajan, Federico Gonzalez, Nilabh Shastri

Abstract read
In one paragraph

Article in Nature immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

54 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
  2. CD8+ Regulatory T Cells.Annual review of immunology · 2026
    Review
  3. Article
  4. The murine MHC-E molecule Qa-1Frontiers in immunology · 2026
    Article
  5. Review
  6. Unconventional CD8Science advances · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Identification of HLA-E BindingJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  16. Innate and Innate-like Effector Lymphocytes in Health and Disease.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Niranjana A NagarajanDepartment of Molecular and Cell Biology, Division of Immunology and Pathogenesis, University of California, Berkeley, California, USA.
Federico Gonzalez
Nilabh Shastri
University of California, Berkeley · US

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
NIAID NIH HHS R01 AI039548NIAID NIH HHS R01 AI044864NIAID NIH HHS R01 AI060040NIAID NIH HHS R21 AI101751NIAID NIH HHS R37 AI060040
6 · The paper itself

Abstract

The aminopeptidase ERAAP is essential for trimming peptides presented by major histocompatibility complex (MHC) class I molecules. Inhibition of ERAAP by cytomegalovirus results in evasion of the immune response by this virus, and polymorphisms in ERAAP are associated with autoimmune disorders. How normal ERAAP function is monitored is unknown. We found that inhibition of ERAAP rapidly induced presentation of the peptide FYAEATPML (FL9) by the MHC class Ib molecule Qa-1(b). Antigen-experienced T cells specific for the Qa-1(b)-FL9 complex were frequent in naive mice. Wild-type mice immunized with ERAAP-deficient cells mounted a potent CD8(+) T cell response specific for Qa-1(b)-FL9. MHC class Ib-restricted cytolytic effector cells specifically eliminated ERAAP-deficient cells in vitro and in vivo. Thus, nonclassical Qa-1(b)-peptide complexes direct cytotoxic T cells to targets with defective antigen processing in the endoplasmic reticulum.

Indexed as

Amino Acid SequenceAnimalsAntigen PresentationCD8-Positive T-LymphocytesCloning, MolecularCytotoxicity Tests, ImmunologicEndoplasmic ReticulumFlow CytometryHistocompatibility Antigens Class IInterferon-gammaLeucyl AminopeptidaseMiceMice, Inbred C57BLMice, KnockoutMolecular Sequence DataReverse Transcriptase Polymerase Chain ReactionHistocompatibility Antigens Class IInterferon-gammaLeucyl Aminopeptidasepuromycin-insensitive leucyl-specific aminopeptidaseQ surface antigensRNA, MessengerTumor Necrosis Factor-alpha

Identifiers

PMID22522492
PMCPMC3362685
OpenAlexW1992099618

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.