Evidence map›Paper›PMID 30242254›Full record

ArticleMucosal immunology2019

E. coli Nissle 1917 is a safe mucosal delivery vector for a birch-grass pollen chimera to prevent allergic poly-sensitization.

P J Sarate, S Heinl, S Poiret, M Drinić, C Zwicker, I Schabussova, C Daniel, U Wiedermann

Erratum issuedOpen access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Mucosal immunology, 2019. 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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

P J SarateInstitute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria.
S HeinlDepartment of Biotechnology, University of Natural Resources and Life Sciences VIBT, Vienna, Austria.
S PoiretUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-Centre d'Infection et d'Immunité de Lille, 59000, Lille, France.
M DrinićInstitute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria.
C ZwickerInstitute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria.
I SchabussovaInstitute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria.
C Daniel *Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-Centre d'Infection et d'Immunité de Lille, 59000, Lille, France. catherine.daniel@ibl.cnrs.fr.
U Wiedermann *Institute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria. ursula.wiedermann@meduniwien.ac.at.
Medical University of Vienna · ATCenter for Infection and Immunity of Lille · FRBOKU University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allergic poly-sensitization affects a large number of allergic patients and poses a great challenge for their treatment. In this study we evaluated the effects of the probiotic Escherichia coli Nissle 1917 (EcN) expressing a birch and grass pollen allergen chimera 'Bet v 1, Phl p 1 and Phl p 5' (EcN-Chim) on allergy prevention after oral or intranasal application in poly-sensitized mice. In contrast to oral application, intranasal pretreatment with EcN-Chim prior to poly-sensitization led to a significant reduction of lung inflammation (eosinophils, IL-5, and IL-13 in bronchoalveolar lavage) along with suppressed levels of allergen-specific serum IgE. The suppression was associated with increased levels of allergen-specific IgA in lungs and serum IgG2a along with increased Foxp3, TGF-β, and IL-10 mRNA in bronchial lymph nodes. In vitro EcN induced high levels of IL-10 and IL-6 in both lung and intestinal epithelial cells. Importantly, using in vivo imaging techniques we demonstrated that intranasally applied EcN do not permanently colonize nose, lung, and gut and this strain might therefore be a safe delivery vector against allergy in humans. In conclusion, our data show that intranasal application of recombinant EcN expressing a multiallergen chimera presents a novel and promising treatment strategy for prevention of allergic poly-sensitization.

Indexed as

AllergensAnimalsAntigens, PlantBetulaCross ReactionsCytokinesEscherichia coliFemaleGenetic VectorsHumansHypersensitivityImmunizationImmunoglobulin EMiceMice, Inbred BALB CMicroorganisms, Genetically-ModifiedAllergensAntigens, PlantBet v 1 allergen, BetulaCytokinesImmunoglobulin EPHLPI protein, Phleum pratensePhl p V protein, Phleum pratensePlant ProteinsRecombinant Fusion Proteins

Identifiers

PMID30242254
OpenAlexW2891208612

What OpenQuestion holds

Textmetadata
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.