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dc.contributor.authorSánchez-Ovejero, Carlos
dc.contributor.authorAkdur, Eylem
dc.contributor.authorManzano-Román, Raúl
dc.contributor.authorHernandez-Gonzalez, Ana 
dc.contributor.authorGonzález-Sánchez, María
dc.contributor.authorBecerro-Recio, David
dc.contributor.authorGonzález-Miguel, Javier
dc.contributor.authorAkhan, Okan
dc.contributor.authorCretu, Carmen M
dc.contributor.authorVutova, Kamenna
dc.contributor.authorTamarozzi, Francesca
dc.contributor.authorMariconti, Mara
dc.contributor.authorBrunetti, Enrico
dc.contributor.authorVola, Ambra
dc.contributor.authorFabiani, Massimo
dc.contributor.authorCasulli, Adriano
dc.contributor.authorSiles-Lucas, Mar
dc.date.accessioned2021-02-05T08:11:22Z
dc.date.available2021-02-05T08:11:22Z
dc.date.issued2020
dc.identifier.citationPLoS Negl Trop Dis . 2020 Nov 30;14(11):e0008892.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/11806
dc.description.abstractCystic echinococcosis (CE) is a neglected zoonotic disease caused by Echinococcus granulosus sensu lato. Diagnosis and monitoring of CE rely primarily on imaging while serology is used as a confirmatory test. However, imaging is not always conclusive and currently available serological assays have suboptimal sensitivity and specificity, lack standardization, and are not useful for patients´ follow-up. Seroassays for CE are usually based on hydatid fluid (HF), a complex, variable antigenic mixture, and cross-reactivity exists especially with alveolar echinococcosis. Recombinant proteins based on immunogenic antigens most abundant in HF, such as AgB1, AgB2 and Ag5, have been used to overcome these limitations. None of them so far showed potential to replace HF; however, their performance have been largely tested on a limited number of samples, and comparison of different antigens using the same cohort has been rarely performed. The combination of several immunogenic epitopes in a single recombinant protein could enhance test sensitivity. For the diagnosis and follow-up of patients with CE, we compared the performance of the crude HF, previously described recombinant 2B2t antigen, and GST-tagged version of 2B2t, and novel designed recombinants (GST-Ag5t and the GST-DIPOL chimera containing AgB1, AgBB2 and Ag5 epitopes) by IgG-ELISA format. Samples belong to a retrospective cohort of 253 well-characterized patients with CE, previously described for the evaluation of the 2B2t antigen, 92 patients with alveolar echinococcosis, and 82 healthy donors. The reference standard for CE diagnosis was the presence of a CE lesion as diagnosed by ultrasonography. The highest sensitivity was obtained with HF [86.7%, 95% confidence interval (CI): 81.2-91.0], followed by GST-2B2t (70.0%, 95% CI: 63.1-76.2), 2B2t (65.5%, 95% CI: 58.5-72.0), GST-Ag5t (64.5%, 95% CI: 57.5-71.1) and GST-DIPOL (63.1%, 95% CI: 56.0-69.7). The GST-2B2t had the best specificity (95.8%, 95% CI: 88.3-99.1) and the lowest cross-reactivity (38.7%, 95% CI: 27.6-50.6). Good response to treatment also correlated to negative test results in the GST-2B2t ELISA. While none of the tested recombinant antigen appears suitable to replace HF for the diagnosis of CE, GST-2B2t should be further explored as a confirmation test, based on its high specificity and low cross-reactivity, and for the follow-up after treatment in those patients with positive serology for this antigen.es_ES
dc.description.sponsorshipThis work was supported by the European Commission Seventh Framework Programme (FP7) under the HERACLES project (grant agreement n 602051; http://www.heracles-fp7.eu/). RMR, OA, CMC, KV, FT, EB, AC AND MSL were supported by the European Commission Seventh Framework Programme (FP7). JGM is supported by the JIN project “ULYSSES” (RTI2018-093463-J-100) (MCIU/AEI/FEDER, UE). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.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.meshAnimals es_ES
dc.subject.meshAntibodies, Helminth es_ES
dc.subject.meshAntigens, Helminth es_ES
dc.subject.meshCohort Studies es_ES
dc.subject.meshCross Reactions es_ES
dc.subject.meshEchinococcosis es_ES
dc.subject.meshEchinococcus granulosus es_ES
dc.subject.meshEnzyme-Linked Immunosorbent Assay es_ES
dc.subject.meshFemale es_ES
dc.subject.meshHumans es_ES
dc.subject.meshImmunoassay es_ES
dc.subject.meshItaly es_ES
dc.subject.meshMale es_ES
dc.subject.meshRecombinant Proteins es_ES
dc.subject.meshRetrospective Studies es_ES
dc.subject.meshSensitivity and Specificity es_ES
dc.subject.meshSerologic Tests es_ES
dc.titleEvaluation of the sensitivity and specificity of GST-tagged recombinant antigens 2B2t, Ag5t and DIPOL in ELISA for the diagnosis and follow up of patients with cystic echinococcosis.es_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID33253168es_ES
dc.format.volume14es_ES
dc.format.number11es_ES
dc.format.pagee0008892es_ES
dc.identifier.doi10.1371/journal.pntd.0008892es_ES
dc.contributor.funderUnión Europea. Comisión Europea. 7 Programa Marco 
dc.description.peerreviewedes_ES
dc.identifier.e-issn1935-2735es_ES
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pntd.0008892es_ES
dc.identifier.journalPLoS neglected tropical diseaseses_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/602051es_ES
dc.rights.accessRightsopen accesses_ES


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