Evidence map›Paper›PMID 23716300›Full record

ArticleEuropean journal of immunology2013

MyD88 and TRIF synergistic interaction is required for TH1-cell polarization with a synthetic TLR4 agonist adjuvant.

Mark T Orr, Malcolm S Duthie, Hillarie Plessner Windish, Elyse A Lucas, Jeffrey A Guderian, Thomas E Hudson, Narek Shaverdian, Joanne O'Donnell, Anthony L Desbien, Steven G Reed and 1 more

Abstract read
In one paragraph

Article in European journal of immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

50 citing papers in PubMed, 75 citations in OpenAlex.

  1. Trial
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  13. Pathological and protective roles of dendritic cells inFrontiers in cellular and infection microbiology · 2022
    Review
  14. Review
  15. Article
  16. Review
  17. Inclusion of an OptimizedJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  18. Advancing Adjuvants forFrontiers in immunology · 2021
    Review
  19. Article
  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

11 authors at 1 institution in 1 country.

Mark T OrrInfectious Disease Research Institute, Seattle, WA, USA.
Malcolm S Duthie
Hillarie Plessner Windish
Elyse A Lucas
Jeffrey A Guderian
Thomas E Hudson
Narek Shaverdian
Joanne O'Donnell
Anthony L Desbien
Steven G Reed
Rhea N Coler
Infectious Disease Research Institute · US

Funding

Development and Manufacture of Adjuvants for Vaccines Targeting MDR TuberculosisU01AI078054 · NIAID · ACCESS TO ADVANCED HEALTH INSTITUTE · PI COLER, RHEA N · 2008 to 2011
$6.2M
NIAID NIH HHS AI-078054NIAID NIH HHS HHSN272200800045CNIAID NIH HHS U01 AI078054
6 · The paper itself

Abstract

Glucopyranosyl lipid adjuvant-stable emulsion (GLA-SE) is a synthetic adjuvant TLR4 agonist that promotes potent poly-functional T(H)1 responses. Different TLR4 agonists may preferentially signal via MyD88 or TIR-domain-containing adapter inducing IFN-beta (TRIF) to exert adjuvant effects; however, the contribution of MyD88 and TRIF signaling to the induction of polyclonal T(H)1 responses by TLR4 agonist adjuvants has not been studied in vivo. To determine whether GLA-SE preferentially signals through MyD88 or TRIF, we evaluated the immune response against a candidate tuberculosis (TB) vaccine Ag following immunization of mice lacking either signaling adapter compared with that of wild-type mice. We find that both MyD88 and TRIF are necessary for GLA-SE to induce a poly-functional T(H)1 immune response characterized by CD4(+) T cells producing IFN-γ, TNF, and IL-2, as well as IgG2c class switching, when paired with the TB vaccine Ag ID93. Accordingly, the protective efficacy of ID93/GLA-SE immunization against aerosolized Mycobacterium tuberculosis was lost when either signaling molecule was ablated. We demonstrate that MyD88 and TRIF must be expressed in the same cell for the in vivo T(H)1-skewing adjuvant activity, indicating that these two signaling pathways cooperate on an intracellular level. Thus engagement of both the MyD88 and TRIF signaling pathways are essential for the effective adjuvant activity of this TLR4 agonist.

Indexed as

Adaptor Proteins, Vesicular TransportAdjuvants, ImmunologicAnimalsCD4-Positive T-LymphocytesDendritic CellsImmunizationImmunoglobulin Class SwitchingInterferon-gammaInterleukin-2MiceMice, Inbred C57BLMice, KnockoutMycobacterium InfectionsMycobacterium tuberculosisMyeloid Differentiation Factor 88Receptors, IgGAdaptor Proteins, Vesicular TransportAdjuvants, ImmunologicIgG2c receptorInterferon-gammaInterleukin-2Myd88 protein, mouseMyeloid Differentiation Factor 88Receptors, IgGTicam1 protein, mouseTlr4 protein, mouseToll-Like Receptor 4Tuberculosis VaccinesTumor Necrosis Factor-alphaAdjuvantCD4+ T cellsGLATLR4Vaccine

Identifiers

PMID23716300
PMCPMC3803998
OpenAlexW1884772424

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.