Evidence map›Paper›PMID 18246202›Full record

ArticleThe Journal of clinical investigation2008

Effects of IL-7 on memory CD8 T cell homeostasis are influenced by the timing of therapy in mice.

Som G Nanjappa, Jane H Walent, Michel Morre, M Suresh

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

54 citing papers in PubMed, 75 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. IL-7 promotes mRNA vaccine-induced long-term immunity.Journal of nanobiotechnology · 2024
    Article
  6. Article
  7. Article
  8. Modifying enzyme replacement therapy - A perspective.Journal of cellular and molecular medicine · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. MicroRNA regulation of CD8Non-coding RNA investigation · 2019
    Article
  19. Review
  20. 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
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Som G NanjappaDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Jane H Walent
Michel Morre
M Suresh
University of Wisconsin–Madison · US

Funding

Regulation of CD8 T Cell Immunity by TNF ReceptorsR01AI048785 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI SURESH, MARULASIDDAPPA · 2002 to 2012
$3.3M
Direct Regulation of CD8 T Cells by Interferon gammaR01AI059804 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI SURESH, MARULASIDDAPPA · 2004 to 2010
$1.4M
Enhancement of CD8 T Cell Immunity by IL-7 TherapyR21AI068841 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI SURESH, MARULASIDDAPPA · 2007 to 2008
$393k
REGULATION OF CD8 T CELL IMMUNITY BY TNF RECEPTORSR21AI048785 · NIAID · UNIVERSITY OF WISCONSIN MADISON · PI SURESH, MARULASIDDAPPA · 2001 to 2001
$291k
NIAID NIH HHS AI48785NIAID NIH HHS AI59804NIAID NIH HHS AI68841NIAID NIH HHS R01 AI048785NIAID NIH HHS R01 AI059804NIAID NIH HHS R21 AI048785NIAID NIH HHS R21 AI068841
6 · The paper itself

Abstract

IL-7 is integral to the generation and maintenance of CD8(+) T cell memory, and insufficient IL-7 is believed to limit survival and the persistence of memory CD8(+) T cells. Here, we show that during the mouse T cell response to lymphocytic choriomeningitis virus, IL-7 enhanced the number of memory CD8(+) T cells when its administration was restricted to the contraction phase of the response. Likewise, IL-7 administration during the contraction phase of the mouse T cell response to vaccinia virus or a DNA vaccine potentiated antigen-specific CD8(+) memory T cell proliferation and function. Qualitatively, CD8(+) T cells from IL-7-treated mice exhibited superior recall responses and improved viral control. IL-7 treatment during the memory phase stimulated a marked increase in the number of memory CD8(+) T cells, but the effects were transient. IL-7 therapy during contraction of the secondary CD8(+) T cell response also expanded the pool of memory CD8(+) T cells. Collectively, our studies show differential effects of IL-7 on memory CD8(+) T cell homeostasis and underscore the importance of the timing of IL-7 therapy to effectively improve CD8(+) T cell memory and protective immunity. These findings may have implications in the clinical use of IL-7 as an immunotherapeutic agent to bolster vaccine-induced CD8(+) T cell memory.

Indexed as

AnimalsCD8-Positive T-LymphocytesHomeostasisImmunologic MemoryInterleukin-7Lymphocyte ActivationLymphocytic ChoriomeningitisMiceMice, Inbred C57BLTime FactorsTumor Necrosis Factor-alphaVaccines, DNAViral VaccinesInterleukin-7Tumor Necrosis Factor-alphaVaccines, DNAViral Vaccines

Identifiers

PMID18246202
PMCPMC2214844
OpenAlexW2157598971

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.