Evidence map›Paper›PMID 16709826›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2006

Clustering class I MHC modulates sensitivity of T cell recognition.

David R Fooksman, Gigi Kwik Grönvall, Qing Tang, Michael Edidin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

33 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Tetraspanin-5-mediated MHC class I clustering is required for optimal CD8 T cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  3. Article
  4. Homotypic and heterotypicCurrent research in immunology · 2022
    Review
  5. Article
  6. Precision engineering of targeted nanocarriers.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2018
    Review
  7. Engineering Platforms for T Cell Modulation.International review of cell and molecular biology · 2018
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Organizing MHC Class II Presentation.Frontiers in immunology · 2014
    Review
  16. Article
  17. Article
  18. Endogenous viral antigen processing generates peptide-specific MHC class I cell-surface clusters.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  19. Article
  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

4 authors at 2 institutions in 2 countries.

David R FooksmanDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Gigi Kwik Grönvall
Qing Tang
Michael Edidin
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

CELLULAR AND MOLECULAR BIOLOGYT32GM007231 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VAN DOREN, MARK B · 1985 to 2020
$18.4M
CHEMISTRY AND DEVELOPMENT OF TRANSPLANTATION ANTIGENSR01AI014584 · NIAID · JOHNS HOPKINS UNIVERSITY · PI EDIDIN, MICHAEL A · 1985 to 2007
$2.8M
MECHANISMS FOR FORMATION OF CELL MEMBRANE DOMAINSR01GM058554 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI EDIDIN, MICHAEL A · 1999 to 2002
$737k
CHEMISTRY AND DEVELOPMENT OF TRANSPLANTATION ANTIGENSR37AI014584 · NIAID · JOHNS HOPKINS UNIVERSITY · PI EDIDIN, MICHAEL A · 1988 to 1997
–
NIAID NIH HHS AI-14584NIAID NIH HHS R01 AI014584NIAID NIH HHS R01 AI014584-39NIGMS NIH HHS GM058554NIGMS NIH HHS T32 GM007231NIGMS NIH HHS T32 GM07231
6 · The paper itself

Abstract

T cell recognition of peptide-MHC is highly specific and is sensitive to very low levels of agonist peptide; however, it is unclear how this effect is achieved or regulated. In this study we show that clustering class I MHC molecules on the cell surface of B lymphoblasts enhances their recognition by mouse and human T cells. We increased clustering of MHC I molecules by two methods, cholesterol depletion and direct cross-linking of a dimerizable MHC construct. Imaging showed that both treatments increased the size and intensity of MHC clusters on the cell surface. Enlarged clusters correlated with enhanced lysis and T cell effector function. Enhancements were peptide-specific and greatest at low concentrations of peptide. Clustering MHC class I enhanced recognition of both strong and weak agonists but not null peptide. Our results indicate that the lateral organization of MHC class I on the cell surface can modulate the sensitivity of T cell recognition of agonist peptide.

Indexed as

AnimalsAntigen PresentationCell Line, TransformedCell MembraneCholesterolCross-Linking ReagentsCytotoxicity, ImmunologicDimerizationDose-Response Relationship, ImmunologicEpitopes, T-LymphocyteHistocompatibility Antigens Class IHumansMiceMice, TransgenicPeptide FragmentsReceptors, Antigen, T-CellCholesterolCross-Linking ReagentsEpitopes, T-LymphocyteHistocompatibility Antigens Class IPeptide FragmentsReceptors, Antigen, T-Cell

Identifiers

PMID16709826
PMCPMC1524854
OpenAlexW1761352586

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.