Evidence map›Paper›PMID 30573663›Full record

ArticleMolecular & cellular proteomics : MCP2019

HLA-DO Modulates the Diversity of the MHC-II Self-peptidome.

Padma P Nanaware, Mollie M Jurewicz, John D Leszyk, Scott A Shaffer, Lawrence J Stern

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2019. 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
2.3field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  7. Review
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  9. Article
  10. Review
  11. Article
  12. Tuning DO:DM Ratios Modulates MHC Class II Immunopeptidomes.Molecular & cellular proteomics : MCP · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. MHC Class II Presentation Is Affected by Polymorphism in theJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  17. Review
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Padma P NanawareFrom the ‡Department of Pathology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
Mollie M JurewiczFrom the ‡Department of Pathology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.ORCID 0000-0001-8482-3060
John D Leszyk§Mass Spectrometry Facility, University of Massachusetts Medical School, Shrewsbury, Massachusetts 01545.
Scott A Shaffer§Mass Spectrometry Facility, University of Massachusetts Medical School, Shrewsbury, Massachusetts 01545.
Lawrence J SternFrom the ‡Department of Pathology, University of Massachusetts Medical School, Worcester, Massachusetts 01605; Lawrence.Stern@umassmed.edu.ORCID 0000-0001-9870-8557
University of Massachusetts Chan Medical School · US

Funding

T cell and transgenic core U19AI109858 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HUSEBY, ERIC S · 2014 to 2018
$11.9M
TRAINING IN IMMUNOLOGY (COMPETITIVE RENEWAL OF AI07439)T32AI007349 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J. · 1989 to 2024
$4.5M
Structure and Function of MHC ProteinsR37AI038996 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J. · 2008 to 2017
$4.1M
HLA-DO / H2-O: modulation of MHC-II peptide diversity and Treg population controlR01AI127869 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J. · 2018 to 2022
$2.7M
Structure and Function of Class II MHC ProteinsR01AI038996 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J · 1996 to 2006
$1.6M
NIAID NIH HHS R01 AI038996NIAID NIH HHS R01 AI127869NIAID NIH HHS R37 AI038996NIAID NIH HHS T32 AI007349NIAID NIH HHS U19 AI109858
6 · The paper itself

Abstract

Presentation of antigenic peptides on MHC-II molecules is essential for tolerance to self and for initiation of immune responses against foreign antigens. DO (HLA-DO in humans, H2-O in mice) is a nonclassical MHC-II protein that has been implicated in control of autoimmunity and regulation of neutralizing antibody responses to viruses. These effects likely are related to a role of DO in selecting MHC-II epitopes, but previous studies examining the effect of DO on presentation of selected CD4 T cell epitopes have been contradictory. To understand how DO modulates MHC-II antigen presentation, we characterized the full spectrum of peptides presented by MHC-II molecules expressed by DO-sufficient and DO-deficient antigen-presenting cells

Indexed as

AnimalsAntigen PresentationCell LineEpitopes, T-LymphocyteHistocompatibility Antigens Class IIHLA-D AntigensHumansImmunodominant EpitopesMiceMice, Inbred C57BLPeptidesEpitopes, T-LymphocyteH-2O antigenHistocompatibility Antigens Class IIHLA-D AntigensHLA-DO antigensImmunodominant EpitopesPeptidesAbsolute quantificationImmunoaffinityImmunology*Label-free quantificationMass SpectrometryPeptidomics

Identifiers

PMID30573663
PMCPMC6398211
OpenAlexW2906544215

What OpenQuestion holds

Textmetadata
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.