Evidence map›Paper›PMID 12374859›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Soluble peptide-MHC monomers cause activation of CD8+ T cells through transfer of the peptide to T cell MHC molecules.

Qing Ge, Jennifer D Stone, M Todd Thompson, Jennifer R Cochran, Mia Rushe, Herman N Eisen, Jianzhu Chen, Lawrence J Stern

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

34 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. DNA origami patterning of synthetic T cell receptors reveals spatial control of the sensitivity and kinetics of signal activation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Trapping or slowing the diffusion of T cell receptors at close contacts initiates T cell signaling.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. SpyAvidin hubs enable precise and ultrastable orthogonal nanoassembly.Journal of the American Chemical Society · 2014
    Article
  16. Nanoscale artificial antigen presenting cells for T cell immunotherapy.Nanomedicine : nanotechnology, biology, and medicine · 2014
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

8 authors at 3 institutions in 1 country.

Qing GeDepartment of Biology, Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Jennifer D Stone
M Todd Thompson
Jennifer R Cochran
Mia Rushe
Herman N Eisen
Jianzhu Chen
Lawrence J Stern
University of Massachusetts Chan Medical School · USCenter for Cancer Research · USMassachusetts Institute of Technology · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Michael Birnbaum · 1985 to 2026
$93.9M
Interdepartmental Biotechnology Training ProgramT32GM008334 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WITTRUP, KARL DANE · 1989 to 2018
$15.2M
Regulation of T Cell HomeostasisR01AI050631 · NIAID · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI CHEN, JIANZHU · 2002 to 2006
$1.6M
PEPTIDES/MHC I COMPLEXES AND CD8+ T CELLSR01CA060686 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI EISEN, HERMAN N · 1993 to 2004
$1.3M
TRANSGENIC MOUSE MODEL FOR ANALYZING T CELL RESPONSESR01AI044478 · NIAID · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI CHEN, JIANZHU · 1998 to 2002
$944k
VACCINES ELICITING CD8 CYTOTOXIC T CELL RESPONSESR01AI044477 · NIAID · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI EISEN, HERMAN N · 1998 to 2002
$931k
NCI NIH HHS CA 14051NCI NIH HHS CA 60686NCI NIH HHS P30 CA014051NCI NIH HHS R01 CA060686NIAID NIH HHS AI 44477NIAID NIH HHS AI 44478NIAID NIH HHS AI 50631NIAID NIH HHS AI 96361NIAID NIH HHS R01 AI050631NIGMS NIH HHS GM 08334NIGMS NIH HHS T32 GM008334
6 · The paper itself

Abstract

T cell receptor (TCR)-mediated activation of CD4(+) T cells is known to require multivalent engagement of the TCR by, for example, oligomeric peptide-MHC complexes. In contrast, for CD8(+) T cells, there is evidence for TCR-mediated activation by univalent engagement of the TCR. We have here compared oligomeric and monomeric L(d) and K(b) peptide-MHC complexes and free peptide as stimulators of CD8(+) T cells expressing the 2C TCR. We found that the monomers are indeed effective in activating naive and effector CD8(+) T cells, but through an unexpected mechanism that involves transfer of peptide from soluble monomers to T cell endogenous MHC (K(b)) molecules. The result is that T cells, acting as antigen-presenting cells, are able to activate other naive T cells.

Indexed as

Amino Acid SequenceAnimalsAntigen PresentationCD8-Positive T-LymphocytesClone CellsHistocompatibility Antigens Class IIn Vitro TechniquesLymphocyte ActivationMiceMice, KnockoutMice, TransgenicModels, ImmunologicalPeptidesReceptors, Antigen, T-CellHistocompatibility Antigens Class IPeptidesReceptors, Antigen, T-Cell

Identifiers

PMID12374859
PMCPMC129758
OpenAlexW1968611188

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.