Evidence map›Paper›PMID 24023895›Full record

ArticlePloS one2013

MHC class II tetramers made from isolated recombinant α and β chains refolded with affinity-tagged peptides.

Peter Braendstrup, Sune Justesen, Thomas Osterbye, Lise Lotte Bruun Nielsen, Roberto Mallone, Lars Vindeløv, Anette Stryhn, Søren Buus

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

  • Erratum issued
  • Erratum issued
5 · Who and what money

Authors and funding

8 authors.

Peter BraendstrupLaboratory of Experimental Immunology, University of Copenhagen, Copenhagen, Denmark ; Allogeneic Hematopoietic Cell Transplantation Laboratory, Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
Sune Justesen
Thomas Osterbye
Lise Lotte Bruun Nielsen
Roberto Mallone
Lars Vindeløv
Anette Stryhn
Søren Buus

Funding

NIAID NIH HHS HHSN272200900045C
6 · The paper itself

Abstract

Targeting CD4+ T cells through their unique antigen-specific, MHC class II-restricted T cell receptor makes MHC class II tetramers an attractive strategy to identify, validate and manipulate these cells at the single cell level. Currently, generating class II tetramers is a specialized undertaking effectively limiting their use and emphasizing the need for improved methods of production. Using class II chains expressed individually in E. coli as versatile recombinant reagents, we have previously generated peptide-MHC class II monomers, but failed to generate functional class II tetramers. Adding a monomer purification principle based upon affinity-tagged peptides, we here provide a robust method to produce class II tetramers and demonstrate staining of antigen-specific CD4+ T cells. We also provide evidence that both MHC class II and T cell receptor molecules largely accept affinity-tagged peptides. As a general approach to class II tetramer generation, this method should support rational CD4+ T cell epitope discovery as well as enable specific monitoring and manipulation of CD4+ T cell responses.

Indexed as

Protein MultimerizationProtein RefoldingAdultAffinity LabelsAgedAmino Acid SequenceBlood DonorsCD4-Positive T-LymphocytesHistocompatibility Antigens Class IIHumansMiddle AgedMolecular Sequence DataPeptidesProtein Structure, QuaternaryProtein SubunitsRecombinant ProteinsAffinity LabelsHistocompatibility Antigens Class IIPeptidesProtein SubunitsRecombinant Proteins

Identifiers

PMID24023895
PMCPMC3759463

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.