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dc.contributor.authorZegeye, Ephrem Debebe
dc.contributor.authorGovasli Larsen, Morten Andreas
dc.contributor.authorSommerfelt, Halvor
dc.contributor.authorPuntervoll, Pål
dc.date.accessioned2022-07-25T13:09:50Z
dc.date.available2022-07-25T13:09:50Z
dc.date.created2018-11-09T12:10:25Z
dc.date.issued2018
dc.identifier.citationHuman Vaccines & Immunotherapeutics. 2018, .
dc.identifier.issn2164-5515
dc.identifier.urihttps://hdl.handle.net/11250/3008246
dc.description.abstractInfection with enterotoxigenic Escherichia coli (ETEC) is an important cause of diarrhea-related illness and death among children under 5 years of age in low– and middle-income countries (LMIC). Recent studies have found that it is the ETEC subtypes that produce the heat-stable enterotoxin (ST), irrespective of whether they also secrete the heat-labile enterotoxin (LT), which contribute most importantly to the disease burden in children from LMIC. Therefore, adding an ST toxoid would importantly complement ongoing ETEC vaccine development efforts. The ST’s potent toxicity, its structural similarity to the endogenous peptides guanylin and uroguanylin, and its poor immunogenicity have all complicated the advancement of ST-based vaccine development. Recent remarkable progress, however, including the unprecedented screening for optimal ST mutants, mapping of cross-reacting ST epitopes and improved ST-carrier coupling strategies (bioconjugation and genetic fusion), enables the rational design of safe, immunogenic, and well-defined ST-based vaccine candidates.
dc.description.abstractDevelopment of an enterotoxigenic Escherichia coli vaccine based on the heat-stable toxin
dc.language.isoeng
dc.relation.urihttps://www.tandfonline.com/doi/pdf/10.1080/21645515.2018.1496768?needAccess=true
dc.titleDevelopment of an enterotoxigenic Escherichia coli vaccine based on the heat-stable toxin
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber11
dc.source.journalHuman Vaccines & Immunotherapeutics
dc.identifier.doi10.1080/21645515.2018.1496768
dc.identifier.cristin1628664
dc.relation.projectNorges forskningsråd: 234364
dc.relation.projectNorges forskningsråd: 260686
dc.relation.projectNorges forskningsråd: 223269
cristin.unitcode7502,0,0,0
cristin.unitnameFolkehelseinstituttet
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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