Evidence map›Paper›PMID 28872828›Full record

ArticleACS nano2017

Bioengineering Bacterially Derived Immunomodulants: A Therapeutic Approach to Inflammatory Bowel Disease.

Lina Herrera Estrada, Huixia Wu, Kevin Ling, Guikai Zhang, Ronen Sumagin, Charles A Parkos, Rheinallt M Jones, Julie A Champion, Andrew S Neish

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Protein and Peptide Nanocluster Vaccines.Current topics in microbiology and immunology · 2021
    Article
  8. Review
  9. Infection and immunity · 2019
    Article
  10. Enzymes as Immunotherapeutics.Bioconjugate chemistry · 2018
    Review
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 2 institutions in 1 country.

Lina Herrera EstradaSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology , 950 Atlantic Drive NW, Atlanta, Georgia 30332, United States.
Huixia WuDepartment of Pathology, Emory University School of Medicine , Whitehead Bldg., 615 Michael Street, Atlanta, Georgia 30322, United States.
Kevin LingSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology , 950 Atlantic Drive NW, Atlanta, Georgia 30332, United States.
Guikai ZhangDepartment of Pathology, Emory University School of Medicine , Whitehead Bldg., 615 Michael Street, Atlanta, Georgia 30322, United States.
Ronen SumaginDepartment of Pathology, Emory University School of Medicine , Whitehead Bldg., 615 Michael Street, Atlanta, Georgia 30322, United States.
Charles A ParkosDepartment of Pathology, Emory University School of Medicine , Whitehead Bldg., 615 Michael Street, Atlanta, Georgia 30322, United States.
Rheinallt M JonesDepartment of Pathology, Emory University School of Medicine , Whitehead Bldg., 615 Michael Street, Atlanta, Georgia 30322, United States.
Julie A ChampionSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology , 950 Atlantic Drive NW, Atlanta, Georgia 30332, United States.ORCID 0000-0002-0260-9392
Andrew S NeishDepartment of Pathology, Emory University School of Medicine , Whitehead Bldg., 615 Michael Street, Atlanta, Georgia 30322, United States.
Emory University · USGeorgia Institute of Technology · US

Funding

Neutrophil interactions with apical ICAM-1 regulate intestinal epithelial homeostK01DK101675 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SUMAGIN, RONEN · 2014 to 2018
$710k
Engineering bacterially derived immunomodulants:a novel IBD therapeutic approachR56DK095074 · NIDDK · GEORGIA INSTITUTE OF TECHNOLOGY · PI CHAMPION, JULIE, NEISH, ANDREW S · 2012 to 2012
$162k
NIDDK NIH HHS K01 DK101675NIDDK NIH HHS R56 DK095074
6 · The paper itself

Abstract

Bacterial enteric pathogens have evolved efficient mechanisms to suppress mammalian inflammatory and immunoregulatory pathways. By exploiting the evolutionary relationship between the gut and pathogenic bacteria, we have developed a potential mucosal therapeutic. Our findings suggest that engineered preparations of the Salmonella acetyltransferase, AvrA, suppress acute inflammatory responses such as those observed in inflammatory bowel disease (IBD). We created 125 nm diameter cross-linked protein nanoparticles directly from AvrA and carrier protein to deliver AvrA in the absence of Salmonella. AvrA nanoparticles are internalized in vitro and in vivo into barrier epithelial and lamina propria monocytic cells. AvrA nanoparticles inhibit inflammatory signaling and confer cytoprotection in vitro, and in murine colitis models, we observe decreased clinical and histological indices of inflammation. Thus, we have combined naturally evolved immunomodulatory proteins with modern bioengineering to produce AvrA nanoparticles, a potential treatment for IBD.

Indexed as

ImmunomodulationProtein EngineeringAnimalsBacterial ProteinsColitisDisease Models, AnimalHumansInflammationInflammatory Bowel DiseasesMiceMice, Inbred C57BLNanoparticlesParticle SizeRatsAvrA protein, Salmonella entericaBacterial Proteinsanti-inflammatorycolitiseffector proteinintracellular deliverynanoparticles

Identifiers

PMID28872828
PMCPMC7653663
OpenAlexW2750748886

What OpenQuestion holds

Textmetadata
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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.