Evidence map›Paper›PMID 27322555›Full record

ArticleOncotarget2016

IL-2 and IL-6 cooperate to enhance the generation of influenza-specific CD8 T cells responding to live influenza virus in aged mice and humans.

Xin Zhou, Jacob W Hopkins, Chongkai Wang, Vinayak Brahmakshatriya, Susan L Swain, George A Kuchel, Laura Haynes, Janet E McElhaney

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  14. Coenzyme Q10 in acute influenza.Influenza and other respiratory viruses · 2019
    Observational
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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

8 authors at 2 institutions in 2 countries.

Xin ZhouUConn Center on Aging and Department of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
Jacob W HopkinsUConn Center on Aging and Department of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
Chongkai WangUConn Center on Aging and Department of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
Vinayak BrahmakshatriyaDepartment of Pathology, University of Massachusetts Medical School, North Worcester, MA, USA.
Susan L SwainDepartment of Pathology, University of Massachusetts Medical School, North Worcester, MA, USA.
George A KuchelUConn Center on Aging and Department of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
Laura HaynesUConn Center on Aging and Department of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
Janet E McElhaneyUConn Center on Aging and Department of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
UConn Health · USUniversity of Massachusetts Chan Medical School · US

Funding

MOLECULAR BIOLOGY COREP01AG021600 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI HAYNES, LAURA · 2003 to 2016
$24.4M
T cell and transgenic core U19AI109858 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HUSEBY, ERIC S · 2014 to 2018
$11.9M
High-resolution single cell profiling of vaccine responsiveness in the elderlyR01AI142086 · NIAID · JACKSON LABORATORY · PI UCAR, DUYGU · 2019 to 2023
$2.9M
T-Cell Responses Predict Influenza Risk in Older AdultsR01AI068265 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MCELHANEY, JANET E. · 2005 to 2010
$2.3M
Immune Response to High-Dose vs. Standard Dose Influenza VaccineR01AG048023 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KUCHEL, GEORGE A, MCELHANEY, JANET E. · 2014 to 2018
$2.1M
NIAID NIH HHS R01 AI068265NIAID NIH HHS R01 AI142086NIAID NIH HHS U19 AI109858NIA NIH HHS P01 AG021600NIA NIH HHS R01 AG048023
6 · The paper itself

Abstract

An age-related decline in cytolytic activity has been described in CD8+ T cells and we have previously shown that the poor CD8+ effector T cell responses to influenza A/H3N2 challenge result from a decline in the proportion and function of these cytolytic T lymphocytes (CTL). Here, we describe that addition of exogenous cytokines to influenza-stimulated PBMC from both aged mice and humans, enhances the generation of influenza specific CD8 CTL by increasing their proliferation and survival. Our data show that the addition of IL-2 and IL-6 to splenocytes from mice previously infected with influenza virus restores the aged CD8+ T cell response to that observed in young mice. In humans, IL-2 plus IL-6 also reduces the proportion of apoptotic effector CD8+ T cells to levels resembling those of younger adults. In HLA-A2+ donors, MHC Class I tetramer staining showed that adding both exogenous IL-2 and IL-6 resulted in greater differentiation into influenza-specific effector CD8+ T cells. Since this effect of IL-2/IL-6 supplementation can be reproduced with the addition of Toll-like receptor agonists, it may be possible to exploit this mechanism and design new vaccines to improve the CD8 T cell response to influenza vaccination in older adults.

Indexed as

AgingAnimalsApoptosisCD8-Positive T-LymphocytesCell ProliferationGranzymesHumansInfluenza A Virus, H3N2 SubtypeInfluenza, HumanInfluenza VaccinesInterleukin-2Interleukin-6Leukocytes, MononuclearMaleMiceMice, Inbred C57BLGranzymesIL2 protein, humanIL6 protein, humanInfluenza VaccinesInterleukin-2Interleukin-6interleukin-6, mouseagingCD8 T cellGerotargetgranzyme Binterleukin-2interleukin-6

Identifiers

PMID27322555
PMCPMC5129923
OpenAlexW2425675432

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.