Evidence map›Paper›PMID 21436066›Full record

ArticleBlood2011

Immunotherapeutic effects of IL-7 during a chronic viral infection in mice.

Som G Nanjappa, Eui Ho Kim, M Suresh

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. 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
1.7field-weighted citation impact, top 16% 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, 57 citations in OpenAlex.

  1. Trial
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  3. Article
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  7. CD8Immunity · 2023
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. CBLB Constrains Inactivated Vaccine-Induced CD8Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  15. 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
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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.

Som G NanjappaDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Eui Ho Kim
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

Viral persistence during chronic viral infections is associated with a progressive loss of T-cell effector function called functional exhaustion. There is therefore a need to develop immunotherapies to remediate the functional deficits of T cells during these infections. We investigated the immunotherapeutic effects of IL-7 during chronic lymphocytic choriomeningitis virus infection in mice. Our results showed that the effects of IL-7 on T cells depend on the viral load, timing, and duration of treatment during the course of the infection. We document that the effectiveness of IL-7 was constrained by high viral load early in the infection, but treatment for at least 3 weeks during declining viral titers mitigated the programmed contraction of CD8 T cells, markedly enhanced the number of high-quality polyfunctional virus-specific CD8 T cells with a nonexhausted phenotype, and accelerated viral control. Mechanistically, the enhancement of CD8 T-cell responses by IL-7 was associated with increased proliferation and induction of Bcl-2, but not with altered levels of PD-1 or Cbl-b. In summary, our results strongly suggest that IL-7 therapy is a potential strategy to bolster the quality and quantity of T-cell responses in patients with chronic viral infections.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell SeparationChronic DiseaseFlow CytometryImmunologic FactorsInterleukin-7Lymphocytic ChoriomeningitisMiceMice, Inbred C57BLImmunologic FactorsInterleukin-7

Identifiers

PMID21436066
PMCPMC3109537
OpenAlexW2039876970

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.