Evidence map›Paper›PMID 19155490›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Endogenously produced IL-4 nonredundantly stimulates CD8+ T cell proliferation.

Suzanne C Morris, Stephanie M Heidorn, De'Broski R Herbert, Charles Perkins, David A Hildeman, Marat V Khodoun, Fred D Finkelman

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. 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
1.5field-weighted citation impact, top 19% 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, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Role of CD28 and CD8International journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. ChronicAmerican journal of physiology. Heart and circulatory physiology · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Foreign antigen-independent memory-phenotype CD4Nature reviews. Immunology · 2018
    Article
  14. IL-2 and Beyond in Cancer Immunotherapy.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2018
    Review
  15. In vivo IL-4 prevents allo-antigen driven CD8Clinical immunology (Orlando, Fla.) · 2017
    Article
  16. Review
  17. Antigen-inexperienced memory CD8Nature reviews. Immunology · 2017
    Article
  18. Article
  19. Article
  20. IL-4 and IL-15 promotion of virtual memory CD8European journal of immunology · 2016
    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

7 authors at 2 institutions in 1 country.

Suzanne C MorrisResearch Service, Cincinnati Veterans Affairs Medical Center, Cincinnati, OH 45220, USA.
Stephanie M Heidorn
De'Broski R Herbert
Charles Perkins
David A Hildeman
Marat V Khodoun
Fred D Finkelman
Veterans Health Administration · USCincinnati Children's Hospital Medical Center · US

Funding

Regulation of Apoptosis in Activated Primary T CellsR01AI057753 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI HILDEMAN, DAVID A · 2005 to 2013
$2.8M
Alternative Macrophage Activation Limits ImmunopathologyR01GM083204 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI HERBERT, DE'BROSKI R · 2007 to 2018
$2.5M
Regulation of CD8+ T Cell Homeostatis by IL-4R01AI070300 · NIAID · UNIVERSITY OF CINCINNATI · PI FINKELMAN, FRED DOUGLASS · 2008 to 2012
$1.9M
IgG Isotype Regulation of Antibody-Mediated DisordersR01AI072040 · NIAID · UNIVERSITY OF CINCINNATI · PI FINKELMAN, FRED DOUGLASS · 2007 to 2011
$1.9M
Cellular targets of IL-4 and IL-13 in worm expulsionR01AI052099 · NIAID · UNIVERSITY OF CINCINNATI · PI FINKELMAN, FRED DOUGLASS · 2003 to 2007
$1.6M
NIAID NIH HHS R01 AI052099NIAID NIH HHS R01 AI057753NIAID NIH HHS R01 AI070300NIAID NIH HHS R01 AI072040NIGMS NIH HHS R01 GM083204
6 · The paper itself

Abstract

T cell proliferation and survival are regulated by the cytokine receptor common gamma-chain-associated cytokines IL-2, IL-7, and IL-15, while IL-4, another gamma-chain-associated cytokine, is thought to primarily affect T cell quality rather than quantity. In contrast, our experiments reveal that endogenously produced IL-4 is a direct, nonredundant, and potent stimulator of CD8(+) T cell proliferation in Ag- and pathogen-induced CD8(+) T cell responses. These stimulatory effects of IL-4 are observed in both BALB/c and C57BL/6 mice and activate both naive and memory/activated phenotype CD8(+) T cells, although the former are stimulated less than are the latter. IL-4 effects are IL-7- and IL-15-independent, but MHC class I-dependent stimulation appears to be required for the mitogenic effect of IL-4 on naive phenotype CD8(+) T cells. Thus, endogenously produced IL-4 is an important regulator of quantitative as well as qualitative aspects of T cell immunity.

Indexed as

Cell ProliferationAnimalsAntigens, DermatophagoidesBystander EffectCD8-Positive T-LymphocytesCell DeathCells, CulturedCell SurvivalFemaleGrowth InhibitorsInterleukin-4Lymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutAntigens, DermatophagoidesGrowth InhibitorsInterleukin-4Recombinant Proteins

Identifiers

PMID19155490
PMCPMC2814185
OpenAlexW1941785397

What OpenQuestion holds

Textmetadata
LicenceTDM
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.