Evidence map›Paper›PMID 15837791›Full record

ArticleThe Journal of biological chemistry2005

Interaction between the CD8 coreceptor and major histocompatibility complex class I stabilizes T cell receptor-antigen complexes at the cell surface.

Linda Wooldridge, Hugo A van den Berg, Meir Glick, Emma Gostick, Bruno Laugel, Sarah L Hutchinson, Anita Milicic, Jason M Brenchley, Daniel C Douek, David A Price and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

115 citing papers in PubMed, 167 citations in OpenAlex.

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  12. NY-ESO-1 antigen: A promising frontier in cancer immunotherapy.Clinical and translational medicine · 2024
    Review
  13. Article
  14. Article
  15. CD3 downregulation identifies high-avidity human CD8 T cells.Clinical and experimental immunology · 2024
    Article
  16. Review
  17. Strategies and rules for tuning TCR-derived therapy.Expert reviews in molecular medicine · 2023
    Review
  18. Review
  19. Article
  20. Review

55 more citing papers are in PubMed but not listed here.

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 2 institutions in 3 countries.

Linda WooldridgeT Cell Modulation Group, Nuffield Department of Medicine, Peter Medawar Building for Pathogen Research, University of Oxford, South Parks Road, Oxford OX1 3SY, United Kingdom.
Hugo A van den Berg
Meir Glick
Emma Gostick
Bruno Laugel
Sarah L Hutchinson
Anita Milicic
Jason M Brenchley
Daniel C Douek
David A Price
Andrew K Sewell
National Institutes of Health · USUniversity of Oxford · GB

Funding

Mechanisms of Immune Activation and Disease Progression in Animal ModelsZIAAI001029 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BRENCHLEY, JASON · 2009 to 2025
$28.2M
T Cell Immune Responses To HIV And Other PathogensZ01AI005033 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI DOUEK, DANIEL CESAR · 2002 to 2008
$951k
Clonal Dynamics of HIV/SIV-specific T cellsZ01AI005066 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI DOUEK, DANIEL CESAR · 2004 to 2008
$704k
Mechanisms of Immune Activation and Disease Progression in Animal ModelsZ01AI001029 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BRENCHLEY, JASON · 2008 to 2008
$455k
Intramural NIH HHS Z01 AI001029Intramural NIH HHS Z99 AI999999Intramural NIH HHS ZIA AI001029Medical Research Council G108/441Wellcome Trust
6 · The paper itself

Abstract

The off-rate (k(off)) of the T cell receptor (TCR)/peptide-major histocompatibility complex class I (pMHCI) interaction, and hence its half-life, is the principal kinetic feature that determines the biological outcome of TCR ligation. However, it is unclear whether the CD8 coreceptor, which binds pMHCI at a distinct site, influences this parameter. Although biophysical studies with soluble proteins show that TCR and CD8 do not bind cooperatively to pMHCI, accumulating evidence suggests that TCR associates with CD8 on the T cell surface. Here, we titrated and quantified the contribution of CD8 to TCR/pMHCI dissociation in membrane-constrained interactions using a panel of engineered pMHCI mutants that retain faithful TCR interactions but exhibit a spectrum of affinities for CD8 of >1,000-fold. Data modeling generates a "stabilization factor" that preferentially increases the predicted TCR triggering rate for low affinity pMHCI ligands, thereby suggesting an important role for CD8 in the phenomenon of T cell cross-reactivity.

Indexed as

AntigensBiophysicsBiotinylationCD8 AntigensCell MembraneDose-Response Relationship, DrugEpitopesFlow CytometryGenes, MHC Class IGenetic EngineeringHerpesvirus 4, HumanHIV-1HumansKineticsLigandsModels, ChemicalAntigensCD8 AntigensCD8 receptorEpitopesLigandsReceptors, Antigen, T-Cell

Identifiers

PMID15837791
PMCPMC2441837
OpenAlexW2160934060

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.