Evidence map›Paper›PMID 23516357›Full record

ArticlePLoS pathogens2013

Cooperativity between CD8+ T cells, non-neutralizing antibodies, and alveolar macrophages is important for heterosubtypic influenza virus immunity.

Brian J Laidlaw, Vilma Decman, Mohammed-Alkhatim A Ali, Michael C Abt, Amaya I Wolf, Laurel A Monticelli, Krystyna Mozdzanowska, Jill M Angelosanto, David Artis, Jan Erikson and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

113 citing papers in PubMed, 148 citations in OpenAlex.

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53 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 1 country.

Brian J LaidlawDepartment of Microbiology and Institute for Immunology, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Vilma Decman
Mohammed-Alkhatim A Ali
Michael C Abt
Amaya I Wolf
Laurel A Monticelli
Krystyna Mozdzanowska
Jill M Angelosanto
David Artis
Jan Erikson
E John Wherry
University of Pennsylvania · USThe Wistar Institute · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
The Impact of Bacterial Co-Infectin on Respiratory Virus-Specific T cell ResponseU19AI083022 · NIAID · WISTAR INSTITUTE · PI SHEN, HAO · 2009 to 2013
$10.7M
PARASITOLOGY: MODERN APPROACHEST32AI007532 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HERBERT, DE'BROSKI R · 1998 to 2022
$5.0M
Memory CD8 T cell subset cooperation via chemokines in protective immunity to infR21AI077098 · NIAID · WISTAR INSTITUTE · PI WHERRY, E. JOHN · 2007 to 2008
$427k
NCI NIH HHS P30 CA016520NIAID NIH HHS AI077098NIAID NIH HHS AI083022NIAID NIH HHS HHSN272201100018CNIAID NIH HHS R21 AI077098NIAID NIH HHS T32 AI007532NIAID NIH HHS U19 AI083022
6 · The paper itself

Abstract

Seasonal epidemics of influenza virus result in ∼36,000 deaths annually in the United States. Current vaccines against influenza virus elicit an antibody response specific for the envelope glycoproteins. However, high mutation rates result in the emergence of new viral serotypes, which elude neutralization by preexisting antibodies. T lymphocytes have been reported to be capable of mediating heterosubtypic protection through recognition of internal, more conserved, influenza virus proteins. Here, we demonstrate using a recombinant influenza virus expressing the LCMV GP33-41 epitope that influenza virus-specific CD8+ T cells and virus-specific non-neutralizing antibodies each are relatively ineffective at conferring heterosubtypic protective immunity alone. However, when combined virus-specific CD8 T cells and non-neutralizing antibodies cooperatively elicit robust protective immunity. This synergistic improvement in protective immunity is dependent, at least in part, on alveolar macrophages and/or other lung phagocytes. Overall, our studies suggest that an influenza vaccine capable of eliciting both CD8+ T cells and antibodies specific for highly conserved influenza proteins may be able to provide heterosubtypic protection in humans, and act as the basis for a potential "universal" vaccine.

Indexed as

Adaptive ImmunityAnimalsAntibodies, NeutralizingAntibodies, ViralAntigens, ViralCD8-Positive T-LymphocytesCell LineCross ProtectionDogsFemaleGlycoproteinsHumansInfluenza A virusInfluenza, HumanInfluenza VaccinesMacrophages, AlveolarAntibodies, NeutralizingAntibodies, ViralAntigens, Viralglycoprotein peptide 33-41, Lymphocytic choriomeningitis virusGlycoproteinsInfluenza VaccinesPeptide FragmentsViral Proteins

Identifiers

PMID23516357
PMCPMC3597515
OpenAlexW2089532164

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.