<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schmid AM</submitter><funding>BioTechMed-Graz Flagship</funding><funding>Austrian Science Fund FWF</funding><funding>European Union</funding><funding>The Government of Lower Austria</funding><funding>OeAD WTZ</funding><funding>OeAD-GmbH</funding><pagination>297</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10588034</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>E. coli O83 (Colinfant Newborn) is a Gram-negative (G-) probiotic bacterium used in the clinic. When administered orally, it reduces allergic sensitisation but not allergic asthma. Intranasal administration offers a non-invasive and convenient delivery method. This route bypasses the gastrointestinal tract and provides direct access to the airways, which are the target of asthma prevention. G- bacteria such as E. coli O83 release outer membrane vesicles (OMVs) to communicate with the environment. Here we investigate whether intranasally administered E. coli O83 OMVs (EcO83-OMVs) can reduce allergic airway inflammation in mice.&lt;h4>Methods&lt;/h4>EcO83-OMVs were isolated by ultracentrifugation and characterised their number, morphology (shape and size), composition (proteins </pubmed_abstract><journal>Cell communication and signaling : CCS</journal><pubmed_title>Extracellular vesicles of the probiotic bacteria E. coli O83 activate innate immunity and prevent allergy in mice.</pubmed_title><pmcid>PMC10588034</pmcid><funding_grant_id>RS 08/2022</funding_grant_id><funding_grant_id>DK W1248-B30</funding_grant_id><funding_grant_id>Project Secretome</funding_grant_id><funding_grant_id>CZ 06/2020</funding_grant_id><funding_grant_id>P 33073</funding_grant_id><funding_grant_id>Danube Allergy Research Cluster</funding_grant_id><funding_grant_id>101066450</funding_grant_id><funding_grant_id>P 34867</funding_grant_id><funding_grant_id>CZ 07/2023</funding_grant_id><pubmed_authors>Schild S</pubmed_authors><pubmed_authors>Schabussova I</pubmed_authors><pubmed_authors>Kerekes D</pubmed_authors><pubmed_authors>Inic-Kanada A</pubmed_authors><pubmed_authors>Wysmolek M</pubmed_authors><pubmed_authors>Thaler M</pubmed_authors><pubmed_authors>Schmidt K</pubmed_authors><pubmed_authors>Wiedermann U</pubmed_authors><pubmed_authors>Kohl P</pubmed_authors><pubmed_authors>Haunstetter M</pubmed_authors><pubmed_authors>Palmfeldt J</pubmed_authors><pubmed_authors>Nejsum P</pubmed_authors><pubmed_authors>Weinmayer T</pubmed_authors><pubmed_authors>Geissler N</pubmed_authors><pubmed_authors>Whitehead B</pubmed_authors><pubmed_authors>Sindelar M</pubmed_authors><pubmed_authors>Hrdy J</pubmed_authors><pubmed_authors>Razim A</pubmed_authors><pubmed_authors>Schmid AM</pubmed_authors><pubmed_authors>Brazhnikov G</pubmed_authors><pubmed_authors>Krcmarova E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Extracellular vesicles of the probiotic bacteria E. coli O83 activate innate immunity and prevent allergy in mice.</name><description>&lt;h4>Background&lt;/h4>E. coli O83 (Colinfant Newborn) is a Gram-negative (G-) probiotic bacterium used in the clinic. When administered orally, it reduces allergic sensitisation but not allergic asthma. Intranasal administration offers a non-invasive and convenient delivery method. This route bypasses the gastrointestinal tract and provides direct access to the airways, which are the target of asthma prevention. G- bacteria such as E. coli O83 release outer membrane vesicles (OMVs) to communicate with the environment. Here we investigate whether intranasally administered E. coli O83 OMVs (EcO83-OMVs) can reduce allergic airway inflammation in mice.&lt;h4>Methods&lt;/h4>EcO83-OMVs were isolated by ultracentrifugation and characterised their number, morphology (shape and size), composition (proteins </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2026-05-28T11:14:31.52Z</modification><creation>2026-05-13T14:22:22.345Z</creation></dates><accession>S-EPMC10588034</accession><cross_references><pubmed>37864211</pubmed><doi>10.1186/s12964-023-01329-4</doi></cross_references></HashMap>