Evidence map›Paper›PMID 23359502›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

IL-2 produced by CD8+ immune T cells can augment their IFN-γ production independently from their proliferation in the secondary response to an intracellular pathogen.

Qila Sa, Jerold Woodward, Yasuhiro Suzuki

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. 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
3.2field-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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Heliyon · 2022
    Article
  4. Article
  5. Article
  6. Robust Immune Response Induced byInternational journal of nanomedicine · 2021
    Article
  7. CD8Science advances · 2020
    Article
  8. Article
  9. Trisomy 21 dysregulates T cell lineages toward an autoimmunity-prone state associated with interferon hyperactivity.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  10. Article
  11. Immunization With a Live-Attenuated RH:ΔFrontiers in microbiology · 2019
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Strain- and Dose-Dependent Reduction ofFrontiers in cellular and infection microbiology · 2017
    Article
  18. Article
  19. 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.

Qila SaDepartment of Microbiology, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
Jerold Woodward
Yasuhiro Suzuki
University of Kentucky · US

Funding

Towards a Vaccine to Prevent ToxoplasmosisU01AI077887 · NIAID · UNIVERSITY OF CHICAGO · PI MCLEOD, RIMA L · 2008 to 2012
$4.2M
Cooperation of CD8+ T cells and phagocytes to eliminate Toxoplasma cystsR01AI095032 · NIAID · UNIVERSITY OF KENTUCKY · PI SUZUKI, YASUHIRO · 2012 to 2023
$4.1M
IFN-gamma production by microglia for prevention of toxoplasmic encephalitisR01AI078756 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI SUZUKI, YASUHIRO · 2008 to 2012
$1.8M
NIAID NIH HHS AI077887NIAID NIH HHS AI078756NIAID NIH HHS AI095032NIAID NIH HHS R01 AI078756NIAID NIH HHS R01 AI095032NIAID NIH HHS U01 AI077887
6 · The paper itself

Abstract

Chronic infection with Toxoplasma gondii induces a potent resistance against reinfection, and IFN-γ production by CD8(+) T cells is crucial for the protective immunity. However, the molecular mechanisms that regulate the secondary response remain to be elucidated. In the current study, we examined the role of IL-2 in IFN-γ production by CD8(+) immune T cells in their secondary responses using T. gondii-specific CD8(+) T cell hybridomas and splenic CD8(+) immune T cells from chronically infected mice. The majority (92%) of CD8(+) T cell hybridomas produced large amounts of IFN-γ only when a low amount (0.5 ng/ml) of exogenous IL-2 was provided in combination with T. gondii Ags. Inhibition of cell proliferation by mitomycin C did not affect the enhancing effect of IL-2 on the IFN-γ production, and significant increases in transcription factor T-bet expression were associated with the IL-2-mediated IFN-γ amplification. Splenic CD8(+) immune T cells produced similar low levels of IL-2 in the secondary response to T. gondii, and a blocking of IL-2 signaling by anti-IL-2Rα Ab or inhibitors of JAK1 and JAK3 significantly reduced IFN-γ production of the T cells. This IL-2-mediated upregulation of IFN-γ production was observed in mitomycin C-treated CD8(+) immune T cells, thus independent from their cell division. Therefore, endogenous IL-2 produced by CD8(+) immune T cells can play an important autocrine-enhancing role on their IFN-γ production in the secondary responses to T. gondii, suggesting an importance of induction of CD8(+) immune T cells with an appropriate IL-2 production for vaccine development.

Indexed as

AnimalsAntibodiesAntigens, ProtozoanCD8-Positive T-LymphocytesCell ProliferationChronic DiseaseFemaleGene Expression RegulationHybridomasInterferon-gammaInterleukin-2Janus Kinase 1Janus Kinase 3MiceMice, Inbred BALB CMitomycinAntibodiesAntigens, ProtozoanInterferon-gammaInterleukin-2Jak1 protein, mouseJak3 protein, mouseJanus Kinase 1Janus Kinase 3MitomycinT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID23359502
PMCPMC3578122
OpenAlexW2131200543

What OpenQuestion holds

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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.