Evidence map›Paper›PMID 11535838›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Single-cell analysis of signal transduction in CD4 T cells stimulated by antigen in vivo.

T Zell, A Khoruts, E Ingulli, J L Bonnevier, D L Mueller, M K Jenkins

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Superresolution imaging reveals nanometer- and micrometer-scale spatial distributions of T-cell receptors in lymph nodes.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  4. Article
  5. Article
  6. Role of antigen persistence and dose for CD4+ T-cell exhaustion and recovery.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  7. Tyramide signal amplification for analysis of kinase activity by intracellular flow cytometry.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2010
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Competition for self ligands restrains homeostatic proliferation of naive CD4 T cells.Proceedings of the National Academy of Sciences of the United States of America · 2003
    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

6 authors at 1 institution in 1 country.

T ZellDepartment of Microbiology, University of Minnesota, Minneapolis, MN 55455, USA.
A Khoruts
E Ingulli
J L Bonnevier
D L Mueller
M K Jenkins
University of Minnesota · US

Funding

Type I interferons in tolerance in the steady stateP01AI035296 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HOGQUIST, KRISTIN A. · 1993 to 2023
$31.1M
TRACKING CD4+ MEMORY T CELLS IN VIVOR01AI039614 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JENKINS, MARC KEVIN · 1996 to 2023
$8.7M
IMMUNOLOGY TRAINING PROGRAMT32AI007313 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Carla Rothlin · 1989 to 2026
$5.7M
COSTIMULATORY SIGNALS IN CD4+ T-CELL ACTIVATIONR01AI027998 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JENKINS, MARC KEVIN · 1989 to 2022
$4.5M
Costimulatory Signals in CD4+ T Cell ActivationR37AI027998 · NIAID · UNIVERSITY OF MINNESOTA · PI JENKINS, MARC KEVIN · 2008 to 2017
$3.7M
REGULATION OF IL-2 GENE EXPRESSION IN T CELL ANERGYR01GM054706 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MUELLER, DANIEL L · 1996 to 2005
$1.3M
NIAID NIH HHS AI07313NIAID NIH HHS AI27998NIAID NIH HHS AI35296NIAID NIH HHS AI39614NIAID NIH HHS P01 AI035296NIAID NIH HHS R01 AI027998NIAID NIH HHS R01 AI039614NIAID NIH HHS R37 AI027998NIAID NIH HHS T32 AI007313NIGMS NIH HHS GM54706NIGMS NIH HHS R01 GM054706
6 · The paper itself

Abstract

Flow cytometry was used to study signaling events in individual CD4 T cells after antigen recognition in the body. Phosphorylation of c-jun and p38 mitogen-activated protein kinase was detected within minutes in all antigen-specific CD4 T cells in secondary lymphoid tissues after injection of peptide antigen into the bloodstream. The remarkable rapidity of this response correlated with the finding that most naive T cells are in constant contact with dendritic antigen-presenting cells. Contrary to predictions from in vitro experiments, antigen-induced c-jun and p38 mitogen-activated protein kinase phosphorylation did not depend on CD28 signals and was insensitive to inhibition by cyclosporin A. Our results highlight the efficiency of the in vivo immune response and underscore the need to verify which signaling pathways identified in vitro actually operate under physiological conditions.

Indexed as

AnimalsAntigen-Presenting CellsAntigensCD28 AntigensCD4-Positive T-LymphocytesCells, CulturedCyclosporineEnzyme ActivationFlow CytometryImmunosuppressive AgentsJNK Mitogen-Activated Protein KinasesLymphocyte ActivationMiceMice, Inbred BALB CMitogen-Activated Protein KinasesOvalbuminAntigensCD28 AntigensCyclosporineImmunosuppressive AgentsJNK Mitogen-Activated Protein KinasesMitogen-Activated Protein KinasesOvalbuminp38 Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-jun

Identifiers

PMID11535838
PMCPMC58555
OpenAlexW2081292558

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.