Evidence map›Paper›PMID 29769270›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Effective Combination Adjuvants Engage Both TLR and Inflammasome Pathways To Promote Potent Adaptive Immune Responses.

Emilie Seydoux, Hong Liang, Natasha Dubois Cauwelaert, Michelle Archer, Nicholas D Rintala, Ryan Kramer, Darrick Carter, Christopher B Fox, Mark T Orr

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 49 citations in OpenAlex.

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  15. TBK1 and IKKε act like an OFF switch to limit NLRP3 inflammasome pathway activation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. NLRP3 inflammasome activation and cell death.Cellular & molecular immunology · 2021
    Review
  17. Pharmacological Activities forFoods (Basel, Switzerland) · 2021
    Review
  18. Review
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  20. Article
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 1 institution in 1 country.

Emilie SeydouxInfectious Disease Research Institute, Seattle, WA 98102; and.
Hong LiangInfectious Disease Research Institute, Seattle, WA 98102; and.ORCID 0000-0003-0940-7723
Natasha Dubois CauwelaertInfectious Disease Research Institute, Seattle, WA 98102; and.
Michelle ArcherInfectious Disease Research Institute, Seattle, WA 98102; and.
Nicholas D RintalaInfectious Disease Research Institute, Seattle, WA 98102; and.ORCID 0000-0002-1655-9189
Ryan KramerInfectious Disease Research Institute, Seattle, WA 98102; and.
Darrick CarterInfectious Disease Research Institute, Seattle, WA 98102; and.ORCID 0000-0001-5901-3402
Christopher B FoxInfectious Disease Research Institute, Seattle, WA 98102; and.
Mark T OrrInfectious Disease Research Institute, Seattle, WA 98102; and mark.orr@idri.org.
Infectious Disease Research Institute · US

Funding

NIAID NIH HHS HHSN272201400041C
6 · The paper itself

Abstract

The involvement of innate receptors that recognize pathogen- and danger-associated molecular patterns is critical to programming an effective adaptive immune response to vaccination. The synthetic TLR4 agonist glucopyranosyl lipid adjuvant (GLA) synergizes with the squalene oil-in-water emulsion (SE) formulation to induce strong adaptive responses. Although TLR4 signaling through MyD88 and TIR domain-containing adapter inducing IFN-β are essential for GLA-SE activity, the mechanisms underlying the synergistic activity of GLA and SE are not fully understood. In this article, we demonstrate that the inflammasome activation and the subsequent release of IL-1β are central effectors of the action of GLA-SE, as infiltration of innate cells into the draining lymph nodes and production of IFN-γ are reduced in ASC

Indexed as

Adaptor Proteins, Vesicular TransportAdenosine TriphosphateAdjuvants, ImmunologicAnimalsAntigensB-LymphocytesCARD Signaling Adaptor ProteinsFemaleGlucosidesImmunity, HumoralInflammasomesInterferon-betaInterferon-gammaInterleukin-1betaInterleukin-2Lipid AAdaptor Proteins, Vesicular TransportAdenosine TriphosphateAdjuvants, ImmunologicAntigensCARD Signaling Adaptor Proteinsglucopyranosyl lipid-AGlucosidesIFNG protein, mouseIL1B protein, mouseIL1R1 protein, mouseInflammasomesInterferon-betaInterferon-gammaInterleukin-1betaInterleukin-2Lipid AMyd88 protein, mouseMyeloid Differentiation Factor 88NLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousePycard protein, mouseReceptors, Interleukin-1 Type ISqualeneTicam1 protein, mouseToll-Like Receptor 4Tumor Necrosis Factor-alphaVaccines

Identifiers

PMID29769270
PMCPMC6008227
OpenAlexW2803462995

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.