Evidence map›Paper›PMID 32389496›Full record

ArticleVaccine2020

Dissociation of TRIF bias and adjuvanticity.

Katharina Richard, Darren J Perkins, Erin M Harberts, Yang Song, Archana Gopalakrishnan, Kari Ann Shirey, Wendy Lai, Alexandra Vlk, Anup Mahurkar, Shreeram Nallar and 3 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  5. Neutrophil diversity and function in health and disease.Signal transduction and targeted therapy · 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 3 institutions in 1 country.

Katharina RichardDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States.
Darren J PerkinsDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States.
Erin M HarbertsDepartment of Microbial Pathogenesis, University of Maryland School of Dentistry (UMSOD), Baltimore, MD, United States.
Yang SongGenome Informatics Core, Institute for Genome Sciences (IGS), UMSOM, Baltimore, MD, United States.
Archana GopalakrishnanDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States.
Kari Ann ShireyDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States.
Wendy LaiDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States.
Alexandra VlkDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States.
Anup MahurkarGenome Informatics Core, Institute for Genome Sciences (IGS), UMSOM, Baltimore, MD, United States.
Shreeram NallarDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States.
Lynn D HawkinsG2D2, Eisai Inc., Cambridge, MA, United States.
Robert K ErnstDepartment of Microbial Pathogenesis, University of Maryland School of Dentistry (UMSOD), Baltimore, MD, United States.
Stefanie N VogelDepartment of Microbiology and Immunology, University of Maryland School of Medicine (UMSOM), Baltimore, MD, United States. Electronic address: svogel@som.umaryland.edu.
University of Maryland, Baltimore · USHuman Genome Sciences (United States) · USEisai (United States) · US

Funding

Signaling Pathways in Innate ImmunityT32AI095190 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Stefanie N. Vogel · 2012 to 2026
$4.7M
Targeting TLR Signaling Pathways to Blunt Pathogen-mediated Acute Lung InjuryR01AI125215 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BLANCO, JORGE C, VOGEL, STEFANIE N. · 2017 to 2021
$2.7M
Macrophage differentiation and disease outcome in influenza infectionR01AI123371 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, STEFANIE N. · 2017 to 2021
$2.7M
Analysis of Cellular Metabolism using Seahhorse TechnologyS10OD025101 · OD · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, STEFANIE N. · 2019 to 2019
$205k
NIAID NIH HHS R01 AI123371NIAID NIH HHS R01 AI125215NIAID NIH HHS T32 AI095190NIH HHS S10 OD025101
6 · The paper itself

Abstract

Toll-like receptors (TLRs), a family of "pattern recognition receptors," bind microbial and host-derived molecules, leading to intracellular signaling and proinflammatory gene expression. TLR4 is unique in that ligand-mediated activation requires the co-receptor myeloid differentiation 2 (MD2) to initiate two signaling cascades: the MyD88-dependent pathway is initiated at the cell membrane, and elicits rapid MAP kinase and NF-κB activation, while the TIR-domain containing adaptor inducing interferon-β (TRIF)-dependent pathway is initiated from TLR4-containing endosomes and results in IRF3 activation. Previous studies associated inflammation with the MyD88 pathway and adjuvanticity with the TRIF pathway. Gram-negative lipopolysaccharide (LPS) is a potent TLR4 agonist, and structurally related molecules signal through TLR4 to differing extents. Herein, we compared monophosphoryl lipid A (sMPL) and E6020, two synthetic, non-toxic LPS lipid A analogs used as vaccine adjuvants, for their capacities to activate TLR4-mediated innate immune responses and to enhance antibody production. In mouse macrophages, high dose sMPL activates MyD88-dependent signaling equivalently to E6020, while E6020 exhibits significantly more activation of the TRIF pathway (a "TRIF bias") than sMPL. Eritoran, a TLR4/MD2 antagonist, competitively inhibited sMPL more strongly than E6020. Despite these differences, sMPL and E6020 adjuvants enhanced antibody responses to comparable extents, with balanced immunoglobulin (Ig) isotypes in two immunization models. These data indicate that a TRIF bias is not necessarily predictive of superior adjuvanticity.

Indexed as

Myeloid Differentiation Factor 88Toll-Like Receptor 4Adaptor Proteins, Vesicular TransportAnimalsDissociative DisordersLipopolysaccharidesMiceToll-Like ReceptorsAdaptor Proteins, Vesicular TransportLipopolysaccharidesMyeloid Differentiation Factor 88Toll-Like Receptor 4Toll-Like ReceptorsAdjuvantE6020LipopolysaccharideSynthetic monophosphoryl lipid AToll-like receptor 4TRIF bias

Identifiers

PMID32389496
PMCPMC7302928
OpenAlexW3023938897

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.