Evidence map›Paper›PMID 29176828›Full record

ArticlePloS one2017

T cell recognition of Mycobacterium tuberculosis peptides presented by HLA-E derived from infected human cells.

Curtis McMurtrey, Melanie J Harriff, Gwendolyn M Swarbrick, Amanda Duncan, Meghan Cansler, Megan Null, Wilfried Bardet, Kenneth W Jackson, Deborah A Lewinsohn, William Hildebrand and 1 more

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. CD8Science advances · 2024
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Protective RNA nanovaccines againstFrontiers in immunology · 2023
    Article
  16. Article
  17. MR1- and HLA-E-Dependent Antigen Presentation ofInternational journal of molecular sciences · 2022
    Review
  18. Article
  19. Article
  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

11 authors.

Curtis McMurtreyDepartment of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City, OK, United States of America.
Melanie J HarriffVA Portland Health Care System, Portland, OR, United States of America.ORCID http://orcid.org/0000-0002-1461-5351
Gwendolyn M SwarbrickDepartment of Pediatric Medicine, Oregon Health and Sciences University, Portland, OR, United States of America.
Amanda DuncanDepartment of Pediatric Medicine, Oregon Health and Sciences University, Portland, OR, United States of America.
Meghan CanslerDepartment of Pediatric Medicine, Oregon Health and Sciences University, Portland, OR, United States of America.
Megan NullDepartment of Pediatric Medicine, Oregon Health and Sciences University, Portland, OR, United States of America.
Wilfried BardetDepartment of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City, OK, United States of America.
Kenneth W JacksonDepartment of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City, OK, United States of America.
Deborah A LewinsohnDepartment of Pediatric Medicine, Oregon Health and Sciences University, Portland, OR, United States of America.
William HildebrandDepartment of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City, OK, United States of America.
David M LewinsohnVA Portland Health Care System, Portland, OR, United States of America.

Funding

Recognition of Mtb-infected Cells by CD8+ T LymphocytesR01AI048090 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEWINSOHN, DAVID M. · 2001 to 2016
$4.2M
Recognition of Mtb-Infected Cells by Non-Classically Restritcted CD8+ T CellsI01BX000533 · VA · PORTLAND VA MEDICAL CENTER · PI LEWINSOHN, DAVID M. · 2011 to 2024
–
BLRD VA I01 BX000533CSRD VA IK2 CX000538NIAID NIH HHS HHSN272200900053CNIAID NIH HHS R01 AI048090
6 · The paper itself

Abstract

HLA-E is a non-conventional MHC Class I molecule that has been recently demonstrated to present pathogen-derived ligands, resulting in the TCR-dependent activation of αβ CD8+ T cells. The goal of this study was to characterize the ligandome displayed by HLA-E following infection with Mycobacterium tuberculosis (Mtb) using an in-depth mass spectrometry approach. Here we identified 28 Mtb ligands derived from 13 different source proteins, including the Esx family of proteins. When tested for activity with CD8+ T cells isolated from sixteen donors, nine of the ligands elicited an IFN-γ response from at least one donor, with fourteen of 16 donors responding to the Rv0634A19-29 peptide. Further evaluation of this immunodominant peptide response confirmed HLA-E restriction and the presence of Rv0634A19-29-reactive CD8+ T cells in the peripheral blood of human donors. The identification of an Mtb HLA-E ligand that is commonly recognized may provide a target for a non-traditional vaccine strategy.

Indexed as

A549 CellsAdultAmino Acid SequenceAntigen PresentationCD8-Positive T-LymphocytesHistocompatibility Antigens Class IHLA-E AntigensHumansLigandsMycobacterium tuberculosisPeptidesSolubilitySpecies SpecificityTuberculosisHistocompatibility Antigens Class IHLA-E AntigensLigandsPeptides

Identifiers

PMID29176828
PMCPMC5703486

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.