Evidence map›Paper›PMID 11606269›Full record

ArticleBiophysical journal2001

T-cell activation by soluble MHC oligomers can be described by a two-parameter binding model.

J D Stone, J R Cochran, L J Stern

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  5. Article
  6. Article
  7. A quantitative view of strategies to engineer cell-selective ligand binding.Integrative biology : quantitative biosciences from nano to macro · 2021
    Article
  8. Article
  9. Article
  10. Relationship of 2D Affinity to T Cell Functional Outcomes.International journal of molecular sciences · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. T-cell receptor affinity and avidity defines antitumor response and autoimmunity in T-cell immunotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  18. A stochastic T cell response criterion.Journal of the Royal Society, Interface · 2012
    Article
  19. Bifunctional Janus microparticles with spatially segregated proteins.Langmuir : the ACS journal of surfaces and colloids · 2012
    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

3 authors at 1 institution in 1 country.

J D StoneDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
J R Cochran
L J Stern
Massachusetts Institute of Technology · US

Funding

Interdepartmental Biotechnology Training ProgramT32GM008334 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WITTRUP, KARL DANE · 1989 to 2018
$15.2M
EMPTY CLASS II MHC ON DENDRITIC CELLS AND MICROGILIAR01AI048833 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J. · 2001 to 2012
$3.7M
NIAID NIH HHS N01-AI48833NIGMS NIH HHS T32-GM08334
6 · The paper itself

Abstract

T-cell activation is essential for initiation and control of immune system function. T cells are activated by interaction of cell-surface antigen receptors with major histocompatibility complex (MHC) proteins on the surface of other cells. Studies using soluble oligomers of MHC-peptide complexes and other types of receptor cross-linking agents have supported an activation mechanism that involves T cell receptor clustering. Receptor clustering induced by incubation of T cells with MHC-peptide oligomers leads to the induction of T-cell activation processes, including downregulation of engaged receptors and upregulation of the cell-surface proteins CD69 and CD25. Dose-response curves for these T-cell activation markers are bell-shaped, with different maxima and midpoints, depending on the valency of the soluble oligomer used. In this study, we have analyzed the activation behavior using a mathematical model that describes the binding of multivalent ligands to cell-surface receptors. We show that a simple equilibrium binding model accurately describes the activation data for CD4(+) T cells treated with MHC-peptide oligomers of varying valency. The model can be used to predict activation and binding behavior for T cells and MHC oligomers with different properties.

Indexed as

Models, BiologicalAntigens, CDAntigens, Differentiation, T-LymphocyteBinding, CompetitiveBinding SitesCD69 AntigensCross-Linking ReagentsDose-Response Relationship, ImmunologicDown-RegulationHumansLectins, C-TypeLymphocyte ActivationMajor Histocompatibility ComplexReceptors, Antigen, T-CellReceptors, Interleukin-2T-LymphocytesAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCross-Linking ReagentsLectins, C-TypeReceptors, Antigen, T-CellReceptors, Interleukin-2

Identifiers

PMID11606269
PMCPMC1301723
OpenAlexW2058260900

What OpenQuestion holds

Textmetadata
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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.