Evidence map›Paper›PMID 23467936›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Exosome-like nanoparticles from intestinal mucosal cells carry prostaglandin E2 and suppress activation of liver NKT cells.

Zhong-Bin Deng, Xiaoying Zhuang, Songwen Ju, Xiaoyu Xiang, Jingyao Mu, Yuelong Liu, Hong Jiang, Lifeng Zhang, James Mobley, Craig McClain and 6 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

49 citing papers in PubMed, 81 citations in OpenAlex.

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  14. Intestinal extracellular vesicles are altered by vertical sleeve gastrectomy.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Article
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  20. Strategies for the use of Extracellular Vesicles for the Delivery of Therapeutics.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Zhong-Bin DengDepartment of Microbiology and Immunology, Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Xiaoying Zhuang
Songwen Ju
Xiaoyu Xiang
Jingyao Mu
Yuelong Liu
Hong Jiang
Lifeng Zhang
James Mobley
Craig McClain
Wenke Feng
William Grizzle
Jun Yan
Donald Miller
Mitchell Kronenberg
Huang-Ge Zhang
University of Louisville · USUniversity of Alabama at Birmingham · USLa Jolla Institute for Immunology · USLouisville VA Medical Center · US

Funding

Plant exosomes non-coding RNA-mediated anti-inflammatory mechanismsR01AT008617 · NCCIH · UNIVERSITY OF LOUISVILLE · PI HUANG-GE ZHANG · 2016 to 2026
$5.7M
Curcumin reverses tumor exosomes-mediated inhibition of myeloid differentiationR01AT004294 · NCCIH · UNIVERSITY OF LOUISVILLE · PI ZHANG, HUANG-GE · 2007 to 2010
$1.4M
Breast tumor exosomal Jak3BP mediated immunosuppressionR01CA116092 · NCI · UNIVERSITY OF LOUISVILLE · PI ZHANG, HUANG-GE · 2005 to 2011
$1.3M
Age related ubiquitin defect on T-cell response to tumorR01CA107181 · NCI · UNIVERSITY OF LOUISVILLE · PI ZHANG, HUANG-GE · 2005 to 2009
$1.1M
Fruit exosome-like particles for therapeutic delivery of extracellular miRNAsUH2TR000875 · NCATS · UNIVERSITY OF LOUISVILLE · PI GUO, PEIXUAN, ZHANG, HUANG-GE · 2013 to 2014
$867k
lung tumor exosome-mediated inflammation promotes tumor progression and growthR01CA137037 · NCI · UNIVERSITY OF LOUISVILLE · PI ZHANG, HUANG-GE · 2009 to 2010
$616k
Exosomal TRAF2-CSN5 complex mediated inflammation promotes tumor growthI01BX000962 · VA · LOUISVILLE VA MEDICAL MEDICAL CENTER · PI ZHANG, HUANG-GE · 2011 to 2014
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BLRD VA I01 BX000962NCATS NIH HHS UH2 TR000875NCCIH NIH HHS R01 AT004294NCCIH NIH HHS R01AT004294NCCIH NIH HHS R01 AT008617NCI NIH HHS R01 CA107181NCI NIH HHS R01CA107181NCI NIH HHS R01 CA116092NCI NIH HHS R01CA116092NCI NIH HHS R01 CA137037NCI NIH HHS R01CA137037
6 · The paper itself

Abstract

Regulation and induction of anergy in NKT cells of the liver can inhibit autoimmune and antitumor responses by mechanisms that are poorly understood. We investigated the effects of PGE2, delivered by intestinal, mucus-derived, exosome-like nanoparticles (IDENs), on NKT cells in mice. In this study, we demonstrate that IDENs migrate to the liver where they induce NKT cell anergy. These effects were mediated by an IDENs' PGE2. Blocking PGE2 synthesis attenuated IDENs inhibition of induction of IFN-γ and IL-4 by α-galactosylceramide (α-GalCer)-stimulated liver NKT cells in a PGE2 E-type prostanoid 2/E-type prostanoid 4 receptor-mediated manner. Proinflammatory conditions enhanced the migration of IDENs to the liver where α-GalCer and PGE2 induced NKT anergy in response to subsequent α-GalCer stimulation. These findings demonstrate that IDENs carrying PGE2 can be transferred from the intestine to the liver, where they act as immune modulators, inducing an anergic-like state of NKT cells. These reagents might be developed as therapeutics for autoimmune liver diseases.

Indexed as

AnimalsCell-Derived MicroparticlesClonal AnergyCyclic AMPCyclic AMP-Dependent Protein KinasesDinoprostoneDisease Models, AnimalExosomesGalactosylceramidesHepatitis, AutoimmuneHumansIntestinal MucosaLiverLymphocyte ActivationMaleMicealpha-galactosylceramideCyclic AMPCyclic AMP-Dependent Protein KinasesDinoprostoneGalactosylceramides

Identifiers

PMID23467936
PMCPMC4396634
OpenAlexW2156717016

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.