Evidence map›Paper›PMID 35597168›Full record

ArticleBiomaterials2022

Robust tolerogenic dendritic cells via push/pull pairing of toll-like-receptor agonists and immunomodulators reduces EAE.

Peter Deak, Hannah Riley Knight, Aaron Esser-Kahn

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Peter DeakPritzker School of Molecular Engineering, University of Chicago, Chicago, IL, 60637, United States. Electronic address: pdeak@uchicago.edu.
Hannah Riley KnightPritzker School of Molecular Engineering, University of Chicago, Chicago, IL, 60637, United States. Electronic address: hrknight@uchicago.edu.
Aaron Esser-KahnPritzker School of Molecular Engineering, University of Chicago, Chicago, IL, 60637, United States. Electronic address: aesserkahn@uchicago.edu.
University of Chicago · US

Funding

Discovery of adjuvants via novel modulation of innate immune pathways for vaccines against influenza75N93019C00041 · NIAID · UNIVERSITY OF CHICAGO · PI ESSER-KAHN, AARON · 2019 to 2024
$10.0M
Determining the Molecular Mechanism of Covalently Linked TLR AgonistsU01AI124286 · NIAID · UNIVERSITY OF CHICAGO · PI ESSER-KAHN, AARON P · 2016 to 2020
$3.2M
Immunoengineering Postdoctoral Training Program - Resubmission - 1T32AI153020 · NIAID · UNIVERSITY OF CHICAGO · PI ALEGRE, MARIA-LUISA, SWARTZ, MELODY ANN · 2021 to 2025
$2.1M
Microparticle Induced Synergistic Toll-Like Receptor Activation Effect on Dendritic Cell Hyper-Responsive Sub-PopulationsF32AI147517 · NIAID · UNIVERSITY OF CHICAGO · PI DEAK, PETER · 2019 to 2020
$127k
NIAID NIH HHS 75N93019C00041NIAID NIH HHS F32 AI147517NIAID NIH HHS T32 AI153020NIAID NIH HHS U01 AI124286
6 · The paper itself

Abstract

A failure of central immune tolerance driven by autoantigen specific T regulatory (Treg) cells is a major cause of many autoimmune diseases. Restoration of proper autoantigen Treg specific response holds promise as a highly effective, long-term therapy for a wide variety of autoimmune diseases. Generating autoantigen specific Tregs remains a challenge due to the non-specific nature of most tolerizing agents and the complexities of generating Tregs in vivo. Here we show a new push/pull method for inducing antigen-specific Treg tolerance via induction of tolerogenic dendritic cells (tolDCs). We identified a combination of three tolerogenic drugs, dexamethasone, simvastatin and SC-514, which when used in combination with toll-like-receptor (TLR) agonists induces an active tolDC phenotype. When the tolerogenic combination was packaged into a liposome with a model antigen such as ovalbumin (OVA), these tolDCs induce differentiation of OVA specific Tregs both ex vivo and in vivo. We examined the tolerizing potential of the combination in an experimental autoimmune encephalomyelitis (EAE) disease model. Given the antigen specificity of this technique, this paper presents an attractive preclinical autoimmune therapy.

Indexed as

Encephalomyelitis, Autoimmune, ExperimentalAdjuvants, ImmunologicAnimalsAutoantigensDendritic CellsImmune ToleranceImmunologic FactorsMiceMice, Inbred C57BLT-Lymphocytes, RegulatoryAdjuvants, ImmunologicAutoantigensImmunologic FactorsAutoimmunityDendritic cellsLiposomeT regulatory cells

Identifiers

PMID35597168
PMCPMC10152544
OpenAlexW4280556946

What OpenQuestion holds

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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.