Evidence map›Paper›PMID 27793997›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Age-Specific Adjuvant Synergy: Dual TLR7/8 and Mincle Activation of Human Newborn Dendritic Cells Enables Th1 Polarization.

Simon D van Haren, David J Dowling, Willemina Foppen, Dennis Christensen, Peter Andersen, Steven G Reed, Robert M Hershberg, Lindsey R Baden, Ofer Levy

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

72 citing papers in PubMed, 96 citations in OpenAlex.

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  15. Precision adjuvants for pediatric vaccines.Science translational medicine · 2024
    Review
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12 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

9 authors at 4 institutions in 2 countries.

Simon D van HarenDivision of Infectious Diseases, Department of Medicine, Boston Children's Hospital, Boston, MA 02115.ORCID 0000-0002-1791-0161
David J DowlingDivision of Infectious Diseases, Department of Medicine, Boston Children's Hospital, Boston, MA 02115.
Willemina FoppenDivision of Infectious Diseases, Department of Medicine, Boston Children's Hospital, Boston, MA 02115.
Dennis ChristensenDepartment of Infectious Disease Immunology, Statens Serum Institut, Copenhagen, DK-2300, Denmark.
Peter AndersenPrecision Vaccines Program, Division of Infectious Diseases, Boston Children's Hospital, Boston, MA 02115.
Steven G ReedPrecision Vaccines Program, Division of Infectious Diseases, Boston Children's Hospital, Boston, MA 02115.
Robert M HershbergVentiRx Pharmaceuticals, Inc., Seattle, WA 98101; and.
Lindsey R BadenPrecision Vaccines Program, Division of Infectious Diseases, Boston Children's Hospital, Boston, MA 02115.
Ofer LevyDivision of Infectious Diseases, Department of Medicine, Boston Children's Hospital, Boston, MA 02115; ofer.levy@childrens.harvard.edu.
Boston Children's Hospital · USStatens Serum Institut · DKBrigham and Women's Hospital · USPDX Pharmaceuticals (United States) · US

Funding

Dissecting the mechanism of age-specific adjuvant synergy in vitro and in vivoU01AI124284 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI LEVY, OFER · 2016 to 2020
$2.9M
Modeling distinct neonatal purine metabolism to inform vaccine developmentR01AI100135 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI LEVY, OFER · 2012 to 2016
$2.5M
Adenosine Shapes Neonatal Toll-like Receptor FunctionR01AI067353 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI LEVY, OFER · 2006 to 2010
$2.1M
NIAID NIH HHS HHSN272201400052CNIAID NIH HHS R01 AI067353NIAID NIH HHS R01 AI100135NIAID NIH HHS U01 AI124284
6 · The paper itself

Abstract

Due to functionally distinct cell-mediated immunity, newborns and infants are highly susceptible to infection with intracellular pathogens. Indeed, neonatal Ag-presenting dendritic cells (DCs) demonstrate impaired Th1 responses to many candidate adjuvants, including most TLR agonists (TLRAs). Combination adjuvantation systems may provide enhanced immune activation but have typically been developed without regard to the age of the target population. We posited that distinct combinations of TLRAs and C-type lectin receptor agonists may enhance Th1 responses of newborn DCs. TLRA/C-type lectin receptor agonist combinations were screened for enhancement of TNF production by human newborn and adult monocyte-derived DCs cultured in 10% autologous plasma or in newborn cord, infant, adult, and elderly whole blood. Monocyte-derived DC activation was characterized by targeted gene expression analysis, caspase-1 and NF-κB studies, cytokine multiplex and naive autologous CD4

Indexed as

Adjuvants, ImmunologicAdolescentAdultAgedAgingCaspase 1Dendritic CellsFemaleHumansInfant, NewbornLectins, C-TypeMaleNF-kappa BReceptors, ImmunologicTh1 CellsToll-Like Receptor 7Adjuvants, ImmunologicCaspase 1CLEC4D protein, humanLectins, C-TypeNF-kappa BReceptors, ImmunologicTLR7 protein, humanTLR8 protein, humanToll-Like Receptor 7Toll-Like Receptor 8

Identifiers

PMID27793997
PMCPMC7386828
OpenAlexW2548306936

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.