Evidence map›Paper›PMID 27847326›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2016

Adsorption of a synthetic TLR7/8 ligand to aluminum oxyhydroxide for enhanced vaccine adjuvant activity: A formulation approach.

Christopher B Fox, Mark T Orr, Neal Van Hoeven, Sarah C Parker, Traci J T Mikasa, Tony Phan, Elyse A Beebe, Ghislain I Nana, Sharvari W Joshi, Mark A Tomai and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

40 citing papers in PubMed, 62 citations in OpenAlex.

  1. Trial
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  6. Design and Synthesis of Polyphenolic Imidazo[4,5-ACS pharmacology & translational science · 2024
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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

13 authors at 4 institutions in 1 country.

Christopher B FoxIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA; Dept of Global Health, University of Washington, Seattle, WA 98104, USA. Electronic address: cfox@idri.org.
Mark T OrrIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA; Dept of Global Health, University of Washington, Seattle, WA 98104, USA.
Neal Van HoevenIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA.
Sarah C ParkerIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA.
Traci J T MikasaIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA.
Tony PhanIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA.
Elyse A BeebeIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA.
Ghislain I NanaIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA.
Sharvari W JoshiIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA.
Mark A Tomai3M Drug Delivery Systems, 3M Center, 275-3E-10, St. Paul, MN 55144, USA.
James Elvecrog3M Drug Delivery Systems, 3M Center, 275-3E-10, St. Paul, MN 55144, USA.
Timothy R FoutsProfectus Biosciences, Inc., Baltimore, MD 21224, USA.
Steven G ReedIDRI, 1616 Eastlake Ave, Seattle, WA 98102, USA; Dept of Global Health, University of Washington, Seattle, WA 98104, USA.
Infectious Disease Research Institute · USKindeva Drug Delivery (United States) · USUniversity of Washington · USProfectus Biosciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For nearly a century, aluminum salts have been the most widely used vaccine adjuvant formulation, and have thus established a history of safety and efficacy. Nevertheless, for extremely challenging disease targets such as tuberculosis or HIV, the adjuvant activity of aluminum salts may not be potent enough to achieve protective efficacy. Adsorption of TLR ligands to aluminum salts facilitates enhanced adjuvant activity, such as in the human papilloma virus vaccine Cervarix®. However, some TLR ligands such as TLR7/8 agonist imidazoquinolines do not efficiently adsorb to aluminum salts. The present report describes a formulation approach to solving this challenge by developing a lipid-based nanosuspension of a synthetic TLR7/8 ligand (3M-052) that facilitates adsorption to aluminum oxyhydroxide via the structural properties of the helper lipid employed. In immunized mice, the aluminum oxyhydroxide-adsorbed formulation of 3M-052 enhanced antibody and TH1-type cellular immune responses to vaccine antigens for tuberculosis and HIV.

Indexed as

Adjuvants, ImmunologicAdsorptionAIDS VaccinesAluminum HydroxideAluminum OxideAnimalsDrug StabilityHumansImidazolesImmunity, CellularImmunity, HumoralLigandsLipidsMiceMice, Inbred C57BLNanoparticlesAdjuvants, ImmunologicAIDS VaccinesAluminum HydroxideAluminum Oxidealuminum oxide hydroxideImidazolesLigandsLipidsQuinolinesToll-Like Receptor 7Toll-Like Receptor 8Tuberculosis Vaccines

Identifiers

PMID27847326
PMCPMC5176129
OpenAlexW2555426966

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.