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A systematic review and meta-analysis of the validation of serological methods for detecting anti-Toxoplasma gondii antibodies in humans and animals

dc.contributor.authorHuertas López, Ana
dc.contributor.authorCantos Barreda, Ana
dc.contributor.authorMartínez-Carrasco, Carlos
dc.contributor.authorIbáñez López, Francisco Javier
dc.contributor.authorMartínez Subiela, Silvia
dc.contributor.authorCerón, José Joaquín
dc.contributor.authorSánchez Sánchez, Roberto
dc.contributor.authorÁlvarez García, Gema
dc.date.accessioned2024-04-22T18:28:19Z
dc.date.available2024-04-22T18:28:19Z
dc.date.issued2024-03-26
dc.description.abstractToxoplasma gondii is a paradigmatic zoonotic parasite from the One Health perspective, since it is broadly distributed and virtually infects all warm-blooded species. A wide variety of serological techniques have been developed to detect T. gondii infection in humans and animals. Our aim was to describe and compare the main characteristics of these serological tests and validation processes and to critically analyze whether these tests meet the standards required to ensure an accurate serological diagnosis. The current systematic review and meta-analysis included 134 studies that were published from 2013 to 2023. QUADAS 2 tool was used to evaluate the quality of the included studies. A total of 52 variables related to the characteristics of the techniques and analytical and diagnostic validation parameters were studied. A wider panel of tests was developed for humans, including techniques exclusively developed for humans that involve costly equipment and the measurement of different Ig isotypes that are considered biomarkers of congenital toxoplasmosis. Studies conducted in humans frequently employed commercial techniques as reference tests, measured different immunoglobulin isotypes with a predominance for IgG (>50%) and discriminated between acute and chronic infections. In animals, the most commonly used reference techniques were in-house tests, which almost exclusively detected IgG. Common limitations identified in a large number of studies were some misunderstandings of the terms “gold standard” and “reference test” and the absence of information about the negative and positive control sera used or the exact cutoff employed, which were independent of the quality of the study. There is a lack of analytical validation, with few evaluations of cross-reactivity with other pathogens. Diagnostic odds ratio values showed that indirect ELISA based on native or chimeric antigens performed better than other tests. The reproducibility of serological test results in both humans and animals is not guaranteed due to a lack of relevant information and analytical validation. Thus, several key issues should be considered in the future, including interlaboratory ring trials.
dc.description.departmentDepto. de Sanidad Animal
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipUniversidad de Murcia
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipFundación Séneca-Agencia de Ciencia y Tecnología de la Región de Murcia
dc.description.statuspub
dc.identifier.citationHuertas-López A, Cantos-Barreda A, Sánchez-Sánchez R, Martínez-Carrasco C, Ibáñez-López FJ, Martínez-Subiela S, Cerón JJ, Álvarez-García G. A systematic review and meta-analysis of the validation of serological methods for detecting anti-Toxoplasma gondii antibodies in humans and animals. Vet Parasitol. 2024 Mar 21;328:110173. doi: 10.1016/j.vetpar.2024.110173. Epub ahead of print. PMID: 38537410.
dc.identifier.doi10.1016/j.vetpar.2024.110173
dc.identifier.essn1873-2550
dc.identifier.issn0304-4017
dc.identifier.officialurlhttps://doi.org/10.1016/j.vetpar.2024.110173
dc.identifier.pmid38537410
dc.identifier.urihttps://hdl.handle.net/20.500.14352/103353
dc.issue.number110173
dc.journal.titleVeterinary Parasitology
dc.language.isoeng
dc.page.final17
dc.page.initial1
dc.publisherElsevier
dc.relation.projectIDUniversidad de Murcia/R-1207/2017
dc.relation.projectIDUniversidad de Murcia/R-1593/2022
dc.relation.projectIDEuropean Union’s Horizon 2020 Research and Innovation Programme/TOXOSOURCESconsortium/One Health European Joint Programme/773830
dc.relation.projectIDSeneca Foundation of Murcia Region/21327/PDGI/19
dc.relation.projectIDSeneca Foundation of Murcia Region/19894/GERM/15
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu616.993.19
dc.subject.keywordMeta-analysis
dc.subject.keywordOne health
dc.subject.keywordSerological techniques
dc.subject.keywordToxoplasma gondii
dc.subject.keywordValidation
dc.subject.ucmParasitología (Veterinaria)
dc.subject.ucmParasitología (Medicina)
dc.subject.ucmSanidad animal
dc.subject.ucmSalud pública (Medicina)
dc.subject.unesco3212 Salud Publica
dc.subject.unesco3207.12 Parasitología
dc.subject.unesco3109.99 Otras
dc.subject.unesco3109 Ciencias Veterinarias
dc.titleA systematic review and meta-analysis of the validation of serological methods for detecting anti-Toxoplasma gondii antibodies in humans and animals
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number328
dspace.entity.typePublication
relation.isAuthorOfPublication2eb795e6-6289-414d-904a-2699a570b874
relation.isAuthorOfPublication7a652f61-dd56-4eaa-b148-f4355647bad6
relation.isAuthorOfPublication.latestForDiscovery2eb795e6-6289-414d-904a-2699a570b874

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