Evidence map›Paper›PMID 23663778›Full record

ArticleCell2013

Single naive CD4+ T cells from a diverse repertoire produce different effector cell types during infection.

Noah J Tubo, Antonio J Pagán, Justin J Taylor, Ryan W Nelson, Jonathan L Linehan, James M Ertelt, Eric S Huseby, Sing Sing Way, Marc K Jenkins

Abstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 304 papers.

0numbers the graph read from it
0cells of the map it votes in
304citing papers in PubMed
–field-weighted citation impact
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

304 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Renaissance of antiviral CD8Nature reviews. Immunology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Noah J TuboDepartment of Microbiology, Center for Immunology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Antonio J Pagán
Justin J Taylor
Ryan W Nelson
Jonathan L Linehan
James M Ertelt
Eric S Huseby
Sing Sing Way
Marc K Jenkins

Funding

Type I interferons in tolerance in the steady stateP01AI035296 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JENKINS, MARC KEVIN · 1993 to 2023
$31.1M
TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
TRAINING IN HEMOGLOBIN &CELL MEMBRANE RESEARCHT32HL007062 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller, Gregory M Vercellotti · 1985 to 2026
$10.3M
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
Protective CD4+ T CellsR01AI103760 · NIAID · UNIVERSITY OF MINNESOTA · PI JENKINS, MARC KEVIN · 2013 to 2022
$4.2M
Costimulatory Signals in CD4+ T Cell ActivationR37AI027998 · NIAID · UNIVERSITY OF MINNESOTA · PI JENKINS, MARC KEVIN · 2008 to 2017
$3.7M
The Immune Pathogenesis of Prenatal Listeria monocytogenes InfectionR01AI100934 · NIAID · UNIVERSITY OF MINNESOTA · PI WAY, SING SING · 2012 to 2016
$2.3M
Regulatory T cells dictate immunity during persistent Salmonella infectionR01AI087830 · NIAID · UNIVERSITY OF MINNESOTA · PI WAY, SING SING · 2010 to 2014
$1.8M
Origin and Control of Self-Reactive TCRsR01DK095077 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HUSEBY, ERIC S · 2012 to 2016
$1.8M
Modular Subunit Vaccine for SalmonellaR01AI066018 · NIAID · UNIVERSITY OF MINNESOTA · PI JENKINS, MARC KEVIN · 2006 to 2010
$1.5M
Stem Cell Biology Training ProgramT32HD060536 · NICHD · UNIVERSITY OF MINNESOTA · PI KAUFMAN, DAN S. · 2010 to 2014
$779k
NCI NIH HHS T32 CA009138NHLBI NIH HHS T32 HL007062NIAID NIH HHS P01 AI035296NIAID NIH HHS R01 AI039614NIAID NIH HHS R01 AI066018NIAID NIH HHS R01 AI087830NIAID NIH HHS R01-AI087830NIAID NIH HHS R01 AI100934NIAID NIH HHS R01-AI100934NIAID NIH HHS R01 AI103760NIAID NIH HHS R01-AI39614NIAID NIH HHS R01-AI66018NIAID NIH HHS R37 AI027998NIAID NIH HHS R37-AI27998NIAID NIH HHS R56 AI066018NIAID NIH HHS T32 AI007313NIAID NIH HHS T32-AI07313NICHD NIH HHS T32 HD060536NICHD NIH HHS T32-HD060536NIDDK NIH HHS F30 DK093242NIDDK NIH HHS F30-DK093242NIDDK NIH HHS R01 DK095077
6 · The paper itself

Abstract

A naive CD4(+) T cell population specific for a microbial peptide:major histocompatibility complex II ligand (p:MHCII) typically consists of about 100 cells, each with a different T cell receptor (TCR). Following infection, this population produces a consistent ratio of effector cells that activate microbicidal functions of macrophages or help B cells make antibodies. We studied the mechanism that underlies this division of labor by tracking the progeny of single naive T cells. Different naive cells produced distinct ratios of macrophage and B cell helpers but yielded the characteristic ratio when averaged together. The effector cell pattern produced by a given naive cell correlated with the TCR-p:MHCII dwell time or the amount of p:MHCII. Thus, the consistent production of effector cell subsets by a polyclonal population of naive cells results from averaging the diverse behaviors of individual clones, which are instructed in part by the strength of TCR signaling.

Indexed as

Cell DifferentiationAnimalsBacterial InfectionsCD4-Positive T-LymphocytesHistocompatibility Antigens Class IIMiceMice, Inbred C57BLReceptors, Antigen, T-CellT-Lymphocyte SubsetsHistocompatibility Antigens Class IIReceptors, Antigen, T-Cell

Identifiers

PMID23663778
PMCPMC3766899

What OpenQuestion holds

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Registered trials

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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.