Evidence map›Paper›PMID 19017955›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Targeting poly(I:C) to the TLR3-independent pathway boosts effector CD8 T cell differentiation through IFN-alpha/beta.

Soo M Ngoi, Michael G Tovey, Anthony T Vella

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

36 citing papers in PubMed, 73 citations in OpenAlex.

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  13. Exploration of Pattern Recognition Receptor Agonists as Candidate Adjuvants.Frontiers in cellular and infection microbiology · 2021
    Review
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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

3 authors at 2 institutions in 2 countries.

Soo M NgoiDepartment of Immunology, University of Connecticut Health Center, Farmington, CT 06030, USA.
Michael G Tovey
Anthony T Vella
UConn Health · USCentre National pour la Recherche Scientifique et Technique (CNRST) · MA

Funding

PROINFLAMMATORY CYTOKINES BLOCK T CELL DEATH IN VIVOR01AI042858 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T · 1999 to 2016
$4.9M
Understanding the Mechanism of 4-1BB ConstimulatiuonR01AI052108 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T · 2003 to 2007
$1.4M
Understanding the mechanism of 4-1BB costimulationR21AI052108 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T. · 2002 to 2002
$326k
NIAID NIH HHS AI52108NIAID NIH HHS R01 AI042858NIAID NIH HHS R01 AI052108NIAID NIH HHS R01 AI428585NIAID NIH HHS R21 AI052108
6 · The paper itself

Abstract

Poly(I:C) is an adjuvant used for antitumor treatment and vaccines because of its prominent effects on CD8 T cells and NK cells. Poly(I:C) binds TLR3 and this interaction is thought to be central for driving cell-mediated immune responses. We investigated the importance of TLR3 in poly(I:C)-mediated endogenous CD8 T cell responses using the pathogenic T cell stimulant Staphylococcus aureus enterotoxin A. While the responsive CD8 T cells expanded comparably in both wild-type and TLR3(-/-) mice, differentiation of effector CD8 T cells was enhanced by poly(I:C) in the TLR3(-/-) mice. A higher percentage of Ag-specific CD8 T cells became IFN-gamma and TNF-alpha producers in the absence of TLR3 signaling. Consistent with this boosted response was the observation that TLR3-deficient cells synthesized less IL-10 compared with TLR3-sufficient cells in response to poly(I:C). Ultimately, however, the fundamental mechanism of CD8 effector T cell differentiation through the TLR3-independent pathway was shown to be completely IFN-alpha/beta-dependent. Administration of IFN-alpha/beta-neutralizing Abs abolished the poly(I:C) effects in TLR3(-/-) mice. These findings reveal specific roles of how dsRNA receptors shape CD8 T cell responses, which should be considered as poly(I:C) is authenticated as a therapeutic adjuvant used in vaccines.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodiesCancer VaccinesCD8-Positive T-LymphocytesCell DifferentiationEnterotoxinsInterferon-alphaInterferon-betaInterferon-gammaInterleukin-10Killer Cells, NaturalMiceMice, KnockoutPoly I-CRNA, Double-StrandedAdjuvants, ImmunologicAntibodiesCancer Vaccinesenterotoxin A, StaphylococcalEnterotoxinsInterferon-alphaInterferon-betaInterferon-gammaInterleukin-10Poly I-CRNA, Double-StrandedTLR3 protein, mouseToll-Like Receptor 3Tumor Necrosis Factor-alpha

Identifiers

PMID19017955
PMCPMC2676428
OpenAlexW2153164882

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.