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dc.contributor.authorGottstein, Bruno
dc.contributor.authorSchneeberger, Marianne
dc.contributor.authorBoubaker, Ghalia
dc.contributor.authorMerkle, Bernadette
dc.contributor.authorHuber, Cristina
dc.contributor.authorSpiliotis, Markus
dc.contributor.authorMüller, Norbert
dc.contributor.authorGarate, Teresa 
dc.contributor.authorDoherr, Marcus G
dc.date.accessioned2018-12-19T10:44:33Z
dc.date.available2018-12-19T10:44:33Z
dc.date.issued2014-06-12
dc.identifier.citationPLoS Negl Trop Dis. 2014 Jun 12;8(6):e2860es_ES
dc.identifier.issn1935-2735es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/6899
dc.description.abstractTwo recombinant Fasciola hepatica antigens, saposin-like protein-2 (recSAP2) and cathepsin L-1 (recCL1), were assessed individually and in combination in enzyme-linked immunosorbent assays (ELISA) for the specific serodiagnosis of human fasciolosis in areas of low endemicity as encountered in Central Europe. Antibody detection was conducted using ProteinA/ProteinG (PAG) conjugated to alkaline phosphatase. Test characteristics as well as agreement with results from an ELISA using excretory-secretory products (FhES) from adult stage liver flukes was assessed by receiver operator characteristic (ROC) analysis, specificity, sensitivity, Youdens J and overall accuracy. Cross-reactivity was assessed using three different groups of serum samples from healthy individuals (n=20), patients with other parasitic infections (n=87) and patients with malignancies (n=121). The best combined diagnostic results for recombinant antigens were obtained using the recSAP2-ELISA (87% sensitivity, 99% specificity and 97% overall accuracy) employing the threshold (cut-off) to discriminate between positive and negative reactions that maximized Youdens J. The findings showed that recSAP2-ELISA can be used for the routine serodiagnosis of chronic fasciolosis in clinical laboratories; the use of the PAG-conjugate offers the opportunity to employ, for example, rabbit hyperimmune serum for the standardization of positive controls.es_ES
dc.description.sponsorshipThe authors received no specific funding for this study.es_ES
dc.language.isoenges_ES
dc.publisherPublic Library of Science (PLOS) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAdolescent es_ES
dc.subject.meshAdult es_ES
dc.subject.meshAged es_ES
dc.subject.meshAged, 80 and over es_ES
dc.subject.meshAnimals es_ES
dc.subject.meshAntibodies, Helminth es_ES
dc.subject.meshEnzyme-Linked Immunosorbent Assay es_ES
dc.subject.meshEurope es_ES
dc.subject.meshFasciola hepatica es_ES
dc.subject.meshFascioliasis es_ES
dc.subject.meshFemale es_ES
dc.subject.meshHumans es_ES
dc.subject.meshMale es_ES
dc.subject.meshMiddle Aged es_ES
dc.subject.meshRecombinant Proteins es_ES
dc.subject.meshSensitivity and Specificity es_ES
dc.subject.meshSerologic Tests es_ES
dc.subject.meshYoung Adult es_ES
dc.subject.meshAntigens, Helminth es_ES
dc.titleComparative assessment of ELISAs using recombinant saposin-like protein 2 and recombinant cathepsin L-1 from Fasciola hepatica for the serodiagnosis of human Fasciolosises_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID24922050es_ES
dc.format.volume8es_ES
dc.format.number6es_ES
dc.format.pagee2860es_ES
dc.identifier.doi10.1371/journal.pntd.0002860es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1935-2735es_ES
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pntd.0002860es_ES
dc.identifier.journalPLoS neglected tropical diseaseses_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES


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Atribución 4.0 Internacional
Este Item está sujeto a una licencia Creative Commons: Atribución 4.0 Internacional