Evidence map›Paper›PMID 18195006›Full record

ArticleThe Journal of biological chemistry2008

Human major histocompatibility complex (MHC) class I molecules with disulfide traps secure disease-related antigenic peptides and exclude competitor peptides.

Steven M Truscott, Xiaoli Wang, Lonnie Lybarger, William E Biddison, Cortez McBerry, John M Martinko, Janet M Connolly, Gerald P Linette, Daved H Fremont, Ted H Hansen and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. 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

11 authors at 4 institutions in 1 country.

Steven M TruscottDepartment of Pathology and Immunology, Division of Oncology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Xiaoli Wang
Lonnie Lybarger
William E Biddison
Cortez McBerry
John M Martinko
Janet M Connolly
Gerald P Linette
Daved H Fremont
Ted H Hansen
Beatriz M Carreno
Washington University in St. Louis · USSouthern Illinois University Carbondale · USNational Institute of Neurological Disorders and Stroke · USUniversity of Arizona · US

Funding

Virology and Smallpox VaccinationsU54AI057160 · NIAID · WASHINGTON UNIVERSITY · PI RAY, RANJIT · 2003 to 2013
$80.9M
SCT PROBES FOR PATHOGEN IMMUNITYR01AI055849 · NIAID · WASHINGTON UNIVERSITY · PI GILLANDERS, WILLIAM E. · 2004 to 2014
$3.3M
CD8 T Cell Recognition of MHC Class IR01AI027568 · NIAID · WASHINGTON UNIVERSITY · PI CONNOLLY, JANET M · 1989 to 2010
$3.3M
SCT PROBES FOR VIRAL IMMUNITYR56AI055849 · NIAID · WASHINGTON UNIVERSITY · PI HANSEN, TED HOWARD · 2009 to 2009
$380k
NIAID NIH HHS AI027568NIAID NIH HHS AI055849NIAID NIH HHS U54-AI057160
6 · The paper itself

Abstract

The ongoing discovery of disease-associated epitopes detected by CD8 T cells greatly facilitates peptide-based vaccine approaches and the construction of multimeric soluble recombinant proteins (e.g. tetramers) for isolation and enumeration of antigen-specific CD8 T cells. Related to these outcomes of epitope discovery is the recent demonstration that MHC class I/peptide complexes can be expressed as single chain trimers (SCTs) with peptide, beta(2)m and heavy chain connected by linkers to form a single polypeptide chain. Studies using clinically relevant mouse models of human disease have shown that SCTs expressed by DNA vaccination are potent stimulators of cytotoxic T lymphocytes. Their vaccine efficacy has been attributed to the fact that SCTs contain a preprocessed and preloaded peptide that is stably displayed on the cell surface. Although SCTs of HLA class I/peptide complexes have been previously reported, they have not been characterized for biochemical stability or susceptibility to exogenous peptide binding. Here we demonstrate that human SCTs remain almost exclusively intact when expressed in cells and can incorporate a disulfide trap that dramatically excludes the binding of exogenous peptides. The mechanistic and practical applications of these findings for vaccine development and T cell isolation/enumeration are discussed.

Indexed as

AnimalsDisulfidesEpitopes, T-LymphocyteHeLa CellsHLA-A2 AntigenHLA-A AntigensHumansMicePeptidesProtein Structure, TertiaryT-Lymphocytes, CytotoxicVaccinationVaccines, DNADisulfidesEpitopes, T-LymphocyteHLA-A*02:01 antigenHLA-A2 AntigenHLA-A AntigensPeptidesVaccines, DNA

Identifiers

PMID18195006
PMCPMC2276332
OpenAlexW2075414892

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.