Evidence map›Paper›PMID 29666167›Full record

ArticleThe Journal of experimental medicine2018

A flexible MHC class I multimer loading system for large-scale detection of antigen-specific T cells.

Jolien J Luimstra, Malgorzata A Garstka, Marthe C J Roex, Anke Redeker, George M C Janssen, Peter A van Veelen, Ramon Arens, J H Frederik Falkenburg, Jacques Neefjes, Huib Ovaa

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Design of solubly expressed miniaturized SMART MHCs.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Article
  7. Empty MHC Class I Protein Production.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Universal open MHC-I molecules for rapid peptide loading and enhanced complex stability across HLA allotypes.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Article
  14. Article
  15. Identification of HLA-E BindingJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  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

10 authors at 2 institutions in 2 countries.

Jolien J LuimstraOncode Institute and Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0001-9742-929X
Malgorzata A GarstkaCore Research Lab, the Second Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, China m.garstka@xjtu.edu.cn.ORCID 0000-0003-2896-7275
Marthe C J RoexDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-5101-2154
Anke RedekerDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.
George M C JanssenCenter for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, Netherlands.
Peter A van VeelenCenter for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, Netherlands.
Ramon ArensDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0001-5058-4110
J H Frederik FalkenburgDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.
Jacques NeefjesOncode Institute and Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, Netherlands j.j.c.neefjes@lumc.nl.ORCID 0000-0001-6763-2211
Huib OvaaOncode Institute and Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, Netherlands h.ovaa@lumc.nl.ORCID 0000-0002-0068-054X
Leiden University Medical Center · NLThe Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adaptive immunity is initiated by T cell recognition of specific antigens presented by major histocompatibility complexes (MHCs). MHC multimer technology has been developed for the detection, isolation, and characterization of T cells in infection, autoimmunity, and cancer. Here, we present a simple, fast, flexible, and efficient method to generate many different MHC class I (MHC I) multimers in parallel using temperature-mediated peptide exchange. We designed conditional peptides for HLA-A*02:01 and H-2K

Indexed as

Protein MultimerizationAmino Acid SequenceAnimalsCD8-Positive T-LymphocytesCytomegalovirusEpitopesHerpesvirus 4, HumanHistocompatibility Antigens Class IHLA-A AntigensHumansMice, Inbred C57BLMonitoring, ImmunologicPeptidesTemperatureT-LymphocytesEpitopesHistocompatibility Antigens Class IHLA-A AntigensPeptides

Identifiers

PMID29666167
PMCPMC5940271
OpenAlexW2803075628

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.