<?xml version="1.0"?><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xmlns:wgs84_pos="http://www.w3.org/2003/01/geo/wgs84_pos" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:rdaGr2="http://rdvocab.info/ElementsGr2" xmlns:oai="http://www.openarchives.org/OAI/2.0/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:dcterms="http://purl.org/dc/terms/"><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-CDYB4BI5/e6890f80-6cf5-4766-a6ae-90f15945fee9/PDF"><dcterms:extent>2238 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-CDYB4BI5/ded07dea-c86d-40c4-b341-31db9a42730c/TEXT"><dcterms:extent>0 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="2005-2025"><edm:begin xml:lang="en">2005</edm:begin><edm:end xml:lang="en">2025</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:doc-CDYB4BI5"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/URN:NBN:SI:spr-8ER5ZBJN" /><dcterms:issued>2021</dcterms:issued><dc:creator>Bratkovič, Tomaž</dc:creator><dc:creator>Vencelj, Ana</dc:creator><dc:format xml:lang="sl">številka:3</dc:format><dc:format xml:lang="sl">letnik:72</dc:format><dc:format xml:lang="sl">str. 211-225</dc:format><dc:identifier>ISSN:0014-8229</dc:identifier><dc:identifier>COBISSID_HOST:70328067</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-CDYB4BI5</dc:identifier><dc:language>sl</dc:language><dc:publisher xml:lang="sl">Slovensko farmacevtsko društvo</dc:publisher><dcterms:isPartOf xml:lang="sl">Farmacevtski vestnik</dcterms:isPartOf><dc:subject xml:lang="sl">Cepiva</dc:subject><dc:subject xml:lang="sl">cepivo informacijske RNA</dc:subject><dc:subject xml:lang="sl">Infekcijske bolezni</dc:subject><dc:subject xml:lang="sl">Klinične raziskave</dc:subject><dc:subject xml:lang="sl">mehanizem delovanja</dc:subject><dc:subject xml:lang="sl">mRNA</dc:subject><dcterms:temporal rdf:resource="2005-2025" /><dc:title xml:lang="sl">Profilaktična cepiva na osnovi informacijske rna proti nalezljivim boleznim| Prophylactic messenger rna-based vaccines against infectious diseases|</dc:title><dc:description xml:lang="sl">Messenger RNA (mRNA) vaccines are an extremely promising vaccine platform, as they allow for immediate response to new pathogen threats. mRNA vaccines are based on introducing genetic information for one or more antigens of a pathogen directly into cells of a vaccinated individual. The transfected cells use this genetic information to transiently express the encoded protein antigen and display it on the cell surface in the form of antigenic peptides bound to major histocompatibility complex, thereby activating T lymphocytes. If the encoded intact antigen is directed to the cell surface or the extracellular space, robust humoral response is also observed. In the last decade, important progress has been made in the areas of enzymatic mRNA synthesis, understanding immunomodulatory properties of exogenous mRNA as well as materials for mRNA delivery, and optimizing transfection and in vivo translation efficiency, leading to approval of first mRNA-based vaccines in the European Union and United States. here, we review the mechanisms of actions, production technologies and current clinical experience with prophylactic mRNA vaccines against infectious diseases</dc:description><dc:description xml:lang="sl">Cepiva na osnovi informacijske RNA (mRNA) predstavljajo izjemno obetavno platformo cepiv, saj omogočajo hiter odziv na grožnje novih patogenov. Temeljijo na vnosu genskega zapisa za enega ali več antigenov povzročitelja nalezljive bolezni neposredno v celice vakcinirane osebe. Na podlagi genske informacije transfecirane celice prehodno izrazijo proteinski antigen in ga predstavijo na svoji površini v obliki peptidov, vezanih na poglavitni kompleks tkivne skladnosti. Tako predstavljene jih zaznajo limfociti T. Če usmerimo antigen na celično membrano ali v zunajcelični prostor, pride tudi do robustnega humoralnega imunskega odziva. V zadnjem desetletju beležimo precejšen napredek na področjih encimske sinteze mRNA, razumevanja imunomodulatornih lastnosti same eksogene mRNA in dostavnih sistemov mRNA-cepiv ter doseganja učinkovite transfekcije in translacije in vivo, kar je omogočilo nedavno odobritev prvih tovrstnih cepiv v Evropski uniji in ZDA. V prispevku predstavljamo mehanizme delovanj, način proizvodnje in dosedanje klinične izkušnje s profilaktičnimi mRNA-cepivi proti nalezljivim boleznim</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:doc-CDYB4BI5"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:doc-CDYB4BI5" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:doc-CDYB4BI5/e6890f80-6cf5-4766-a6ae-90f15945fee9/PDF" /><edm:rights rdf:resource="http://rightsstatements.org/vocab/InC/1.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Slovensko farmacevtsko društvo</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:doc-CDYB4BI5/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:doc-CDYB4BI5" /></ore:Aggregation></rdf:RDF>