Evidence map›Paper›PMID 36442096›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Human T cells recognize HLA-DP-bound peptides in two orientations.

Sebastian Klobuch, Jia Jia Lim, Peter van Balen, Michel G D Kester, Wendy de Klerk, Arnoud H de Ru, Cilia R Pothast, Inge Jedema, Jan W Drijfhout, Jamie Rossjohn and 4 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. 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
2.2field-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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  4. Re-evaluation of the contribution ofJournal of human immunity · 2025
    Article
  5. Sideways lipid presentation by the antigen-presenting molecule CD1c.bioRxiv : the preprint server for biology · 2025
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  12. Accurate modeling of peptide-MHC structures with AlphaFold.Structure (London, England : 1993) · 2024
    Article
  13. Review
  14. Article
  15. Article
  16. Article
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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

14 authors at 2 institutions in 3 countries.

Sebastian KlobuchDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0003-1364-0763
Jia Jia LimInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0002-6097-6238
Peter van BalenDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-9670-4664
Michel G D KesterDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-8960-7348
Wendy de KlerkDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Arnoud H de RuCenter for Proteomics and Metabolomics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Cilia R PothastDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-9761-3123
Inge JedemaDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0001-9042-6459
Jan W DrijfhoutDepartment of Immunology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0003-4808-5296
Jamie RossjohnInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0002-2020-7522
Hugh H ReidInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0001-6929-5001
Peter A van VeelenCenter for Proteomics and Metabolomics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
J H Frederik FalkenburgDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Mirjam H M HeemskerkDepartment of Hematology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Leiden University Medical Center · NLAustralian Regenerative Medicine Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human leukocyte antigen (HLA) molecules present small peptide antigens to T cells, thereby allowing them to recognize pathogen-infected and cancer cells. A central dogma over the last 50+ y is that peptide binding to HLA molecules is mediated by the docking of side chains of particular amino acids in the peptide into pockets in the HLA molecules in a conserved N- to C-terminal orientation. Whether peptides can be presented in a reversed C- to N-terminal orientation remains unclear. Here, we performed large-scale identification of peptides bound to HLA-DP molecules and observed that in addition to peptide binding in an N- to C-terminal orientation, in 9 out of 14 HLA-DP allotypes, reverse motifs are found, compatible with C- to N-terminal peptide binding. Moreover, we isolated high-avidity human cytomegalovirus (CMV)-specific HLA-DP-restricted CD4

Indexed as

Cytomegalovirus InfectionsPeptidesAmino AcidsCytomegalovirusHistocompatibility Antigens Class IIHLA-DP AntigensHumansT-LymphocytesAmino AcidsHistocompatibility Antigens Class IIHLA-DP AntigensPeptidesHLA-DPreverse peptidesT cell

Identifiers

PMID36442096
PMCPMC9894132
OpenAlexW4310787824

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.