Evidence map›Paper›PMID 35370095›Full record

ReviewTrends in immunology2022

Antigen presentation by MHC-E: a putative target for vaccination?

Linda Voogd, Paula Ruibal, Tom H M Ottenhoff, Simone A Joosten

Open access · greenAbstract readReview
In one paragraph

Review in Trends in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Vaccines · 2024
    Article
  11. bioRxiv : the preprint server for biology · 2024
    Article
  12. iScience · 2024
    Article
  13. Instability of the HLA-E peptidome of HIV presents a major barrier to therapeutic targeting.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  14. Review
  15. Article
  16. Review
  17. HLA-E/Frontiers in immunology · 2024
    Article
  18. Article
  19. Human CD8Immune network · 2023
    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

4 authors at 1 institution in 1 country.

Linda VoogdDepartment of Infectious Diseases, Leiden University Medical Center, Building 1, Albinusdreef 2, 2333ZA, Leiden, The Netherlands.
Paula RuibalDepartment of Infectious Diseases, Leiden University Medical Center, Building 1, Albinusdreef 2, 2333ZA, Leiden, The Netherlands.
Tom H M OttenhoffDepartment of Infectious Diseases, Leiden University Medical Center, Building 1, Albinusdreef 2, 2333ZA, Leiden, The Netherlands.
Simone A JoostenDepartment of Infectious Diseases, Leiden University Medical Center, Building 1, Albinusdreef 2, 2333ZA, Leiden, The Netherlands. Electronic address: s.a.joosten@lumc.nl.
Leiden University Medical Center · NL

Funding

HLA-E restricted T-cell immunity in Mycobacterium tuberculosis infectionR01AI141315 · NIAID · LEIDEN UNIVERSITY MEDICAL CENTER · PI JOOSTEN, SIMONE ANNE · 2019 to 2022
$1.7M
In depth characterization of Mtb specific HLA-E restricted human CD8+ T-cellsR21AI127133 · NIAID · LEIDEN UNIVERSITY MEDICAL CENTER · PI OTTENHOFF, TOM · 2016 to 2017
$281k
NIAID NIH HHS R01 AI141315NIAID NIH HHS R21 AI127133
6 · The paper itself

Abstract

The essentially monomorphic human antigen presentation molecule HLA-E is an interesting candidate target to enable vaccination irrespective of genetic diversity. Predictive HLA-E peptide-binding motifs have been refined to facilitate HLA-E peptide discovery. HLA-E can accommodate structurally divergent peptides of both self and microbial origin. Intracellular processing and presentation pathways for peptides by HLA-E for T cell receptor (TCR) recognition remain to be elucidated. Recent studies show that, unlike canonical peptides, inhibition of the transporter associated with antigen presentation (TAP) is essential to allow HLA-E antigen presentation in cytomegalovirus (CMV) infection and possibly also of other non-canonical peptides. We propose three alternative and TAP-independent MHC-E antigen-presentation pathways, including for Mycobacterium tuberculosis infections. These insights may help in designing potential HLA-E targeting vaccines against tumors and pathogens.

Indexed as

Antigen PresentationTuberculosisHistocompatibility Antigens Class IHumansMembrane Transport ProteinsPeptidesVaccinationHistocompatibility Antigens Class IMembrane Transport ProteinsPeptidesantigen presentationMHC-Epeptide recognitionT cellvaccine

Identifiers

PMID35370095
PMCPMC9058203
OpenAlexW4220697536

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.