Evidence map›Paper›PMID 27005810›Full record

ArticleVaccine2016

Sterile inflammation induced by Carbopol elicits robust adaptive immune responses in the absence of pathogen-associated molecular patterns.

Kate H Gartlan, George Krashias, Frank Wegmann, William R Hillson, Erin M Scherer, Philip D Greenberg, Stephanie C Eisenbarth, Amin E Moghaddam, Quentin J Sattentau

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  10. A potent novel vaccine adjuvant based on straight polyacrylate.International journal of pharmaceutics: X · 2020
    Article
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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

9 authors at 3 institutions in 2 countries.

Kate H GartlanSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK. Electronic address: Kate.Gartlan@qimrberghofer.edu.au.
George KrashiasSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Frank WegmannSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
William R HillsonSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Erin M SchererFred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Philip D GreenbergFred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Stephanie C EisenbarthDepartment of Immunobiology, Yale University, New Haven, CT 06519-1612, USA.
Amin E MoghaddamSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Quentin J SattentauSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
University of Oxford · GBFred Hutch Cancer Center · USYale University · US

Funding

Medical Research Council G0000635
6 · The paper itself

Abstract

Carbopol is a polyanionic carbomer used in man for topical application and drug delivery purposes. However parenteral administration of Carbopol in animal models results in systemic adjuvant activity including strong pro-inflammatory type-1 T-cell (Th1) polarization. Here we investigated potential pathways of immune activation by Carbopol by comparison with other well-characterized adjuvants. Carbopol administration triggered rapid and robust leukocyte recruitment, pro-inflammatory cytokine secretion and antigen capture largely by inflammatory monocytes. The induction of antigen specific Th1 cells by Carbopol was found to occur via a non-canonical pathway, independent of MyD88/TRIF signaling and in the absence of pattern-recognition-receptor (PRR) activation typically associated with Th1/Ig2a induction. Using multispectral fluorescence imaging (Imagestream) and electron microscopy we demonstrated that phagocytic uptake of Carbopol particles followed by entry into the phagosomal/lysosomal pathway elicited conformational changes to the polymer and reactive oxygen species (ROS) production. We therefore conclude that Carbopol may mediate its adjuvant activity via novel mechanisms of antigen presenting cell activation and Th1 induction, leading to enhanced IgG2a responses independent of microbial pattern recognition.

Indexed as

Adaptive ImmunityPathogen-Associated Molecular Pattern MoleculesAcrylic ResinsAdjuvants, ImmunologicAnimalsAntigen-Presenting CellsCell LineChemokinesCytokinesHumansImmunoglobulin GInflammationMice, 129 StrainMice, Inbred BALB CMice, Inbred C57BLPhagocytosisAcrylic ResinsAdjuvants, ImmunologiccarboxypolymethyleneChemokinesCytokinesImmunoglobulin GPathogen-Associated Molecular Pattern MoleculesAntibodiesHIV-1Polyanionic carbomerTh1 immune responsesVaccine adjuvant

Identifiers

PMID27005810
PMCPMC4850248
OpenAlexW2304140687

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.