Evidence map›Paper›PMID 21098221›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

A role for IL-15 in the migration of effector CD8 T cells to the lung airways following influenza infection.

Katherine C Verbist, Charles J Cole, Mary B Field, Kimberly D Klonowski

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.8field-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

45 citing papers in PubMed, 65 citations in OpenAlex.

  1. CD8MedComm · 2026
    Review
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  9. Responsiveness to interleukin-15 therapy is shared between tissue-resident and circulating memory CD8Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Review
  11. Review
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  15. Article
  16. Control of memory CD8Molecular immunology · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. CD4Journal of immunology (Baltimore, Md. : 1950) · 2018
    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

4 authors at 1 institution in 1 country.

Katherine C VerbistDepartment of Cellular Biology, University of Georgia, Athens, GA 30602, USA.
Charles J Cole
Mary B Field
Kimberly D Klonowski
University of Georgia · US

Funding

Cytokine regulation of memory CD8 T cell responsesR01AI081800 · NIAID · UNIVERSITY OF GEORGIA · PI KLONOWSKI, KIMBERLY D. · 2009 to 2013
$1.4M
Memory Cell Migration Following Influenza virus InfectionR21AI077038 · NIAID · UNIVERSITY OF GEORGIA · PI KLONOWSKI, KIMBERLY D. · 2007 to 2008
$401k
NIAID NIH HHS AI077038NIAID NIH HHS AI081800NIAID NIH HHS R01 AI081800NIAID NIH HHS R21 AI077038
6 · The paper itself

Abstract

The cytokines generated locally in response to infection play an important role in CD8 T cell trafficking, survival, and effector function, rendering these signals prime candidates for immune intervention. In this paper, we show that localized increases in the homeostatic cytokine IL-15 induced by influenza infection is responsible for the migration of CD8 effector T cells to the site of infection. Moreover, intranasal delivery of IL-15-IL-15Rα soluble complexes (IL-15c) specifically restores the frequency of effector T cells lost in the lung airways of IL-15-deficient animals after influenza infection. Exogenous IL-15c quantitatively augments the respiratory CD8 T cell response, and continued administration of IL-15c throughout the contraction phase of the anti-influenza CD8 T cell response magnifies the resultant CD8 T cell memory generated in situ. This treatment extends the ability of these cells to protect against heterologous infection, immunity that typically depreciates over time. Overall, our studies describe what to our knowledge is a new function for IL-15 in attracting effector CD8 T cells to the lung airways and suggest that adjuvanting IL-15 could be used to prolong anti-influenza CD8 T cell responses at mucosal surfaces to facilitate pathogen elimination.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell DifferentiationCell MovementImmunologic MemoryInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInterleukin-15LungMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicOrthomyxoviridae InfectionsPneumonia, ViralRespiratory Tract InfectionsInterleukin-15

Identifiers

PMID21098221
PMCPMC3050553
OpenAlexW2103125003

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.