Evidence map›Paper›PMID 19935657›Full record

ArticleNature immunology2010

Different routes of bacterial infection induce long-lived TH1 memory cells and short-lived TH17 cells.

Marion Pepper, Jonathan L Linehan, Antonio J Pagán, Traci Zell, Thamotharampillai Dileepan, P Patrick Cleary, Marc K Jenkins

Abstract read
In one paragraph

Article in Nature immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 195 papers.

0numbers the graph read from it
0cells of the map it votes in
195citing 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

195 citing papers in PubMed.

  1. A phenotypically and functionally distinct human TScience translational medicine · 2017
    Trial
  2. Trial
  3. Review
  4. Article
  5. bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. A guide to adaptive immune memory.Nature reviews. Immunology · 2024
    Review
  10. Article
  11. The dynamics and longevity of circulating CD4bioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. CD4Nature immunology · 2023
    Review
  16. Article
  17. Article
  18. Transcriptional programming of CD4Science immunology · 2023
    Article
  19. Review
  20. Human CCR6bioRxiv : the preprint server for biology · 2023
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Marion PepperDepartment of Microbiology, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
Jonathan L Linehan
Antonio J Pagán
Traci Zell
Thamotharampillai Dileepan
P Patrick Cleary
Marc K Jenkins

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
TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
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
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
NCI NIH HHS T32 CA009138NCI NIH HHS T32-CA9138NIAID NIH HHS AI27998NIAID NIH HHS AI39614NIAID NIH HHS AI66016NIAID NIH HHS P01 AI035296NIAID NIH HHS R01 AI027998NIAID NIH HHS R01 AI039614NIAID NIH HHS R37 AI027998NIAID NIH HHS T32 AI007313NIAID NIH HHS T32-AI07313
6 · The paper itself

Abstract

We used a sensitive method based on tetramers of peptide and major histocompatibility complex II (pMHCII) to determine whether CD4(+) memory T cells resemble the T helper type 1 (T(H)1) and interleukin 17 (IL-17)-producing T helper (T(H)17) subsets described in vitro. Intravenous or intranasal infection with Listeria monocytogenes induced pMHCII-specific CD4(+) naive T cells to proliferate and produce effector cells, about 10% of which resembled T(H)1 or T(H)17 cells, respectively. T(H)1 cells were also present among the memory cells that survived 3 months after infection, whereas T(H)17 cells disappeared. The short lifespan of T(H)17 cells was associated with small amounts of the antiapoptotic protein Bcl-2, the IL-15 receptor and the receptor CD27, and little homeostatic proliferation. These results suggest that T(H)1 cells induced by intravenous infection are more efficient at entering the memory pool than are T(H)17 cells induced by intranasal infection.

Indexed as

Amino Acid SequenceAnimalsCD4-Positive T-LymphocytesCell DifferentiationCell LineCell ProliferationCell SurvivalClone CellsFlow CytometryHistocompatibility Antigens Class IIHost-Pathogen InteractionsImmunologic MemoryInterferon-gammaInterleukin-17Listeria monocytogenesListeriosisHistocompatibility Antigens Class IIInterferon-gammaInterleukin-17Proto-Oncogene Proteins c-bcl-2Receptors, Interleukin-15Tumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID19935657
PMCPMC2795784

What OpenQuestion holds

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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.