dc.creatorVolta, Bibiana J.
dc.creatorBustos, Patricia L.
dc.creatorCardoni, Rita L.
dc.creatorDe Rissio, Ana María
dc.creatorLaucella, Susana A.
dc.creatorBua, Jacqueline
dc.date2019-12-04T19:31:43Z
dc.date2019-12-04T19:31:43Z
dc.date2016-06-01
dc.date.accessioned2023-08-29T20:06:23Z
dc.date.available2023-08-29T20:06:23Z
dc.identifier1550-6606
dc.identifierhttp://sgc.anlis.gob.ar/handle/123456789/1435
dc.identifier10.4049/jimmunol.1502504
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8519129
dc.descriptionFil: Volta, Bibiana J. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología; Argentina.
dc.descriptionFil: Bustos, Patricia L. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología; Argentina.
dc.descriptionFil: Cardoni, Rita L. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología; Argentina.
dc.descriptionFil: De Rissio, Ana María. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología; Argentina.
dc.descriptionFil: Laucella, Susana A. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología; Argentina.
dc.descriptionFil: Bua, Jacqueline. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología; Argentina.
dc.descriptionTrypanosoma cruzi, the causing agent of Chagas disease, leads to an activation of the immune system in congenitally infected infants. In this study, we measured a set of cytokines/chemokines and the levels of parasitemia by quantitative PCR in the circulation of neonates born to T. cruzi-infected mothers to evaluate the predictive value of these mediators as biomarkers of congenital transmission. We conducted a retrospective cohort study of 35 infants with congenital T. cruzi infection, of which 15 and 10 infants had been diagnosed by detection of parasites by microscopy in the first and sixth month after delivery, respectively, and the remaining 10 had been diagnosed by the presence of T. cruzi-specific Abs at 10-12 mo old. Uninfected infants born to either T. cruzi-infected or uninfected mothers were also evaluated as controls. The plasma levels of IL-17A, MCP-1, and monokine induced by IFN-γ were increased in infants congenitally infected with T. cruzi, even before they developed detectable parasitemia or seroconversion. Infants diagnosed between 6 and 12 mo old also showed increased levels of IL-6 and IL-17F at 1 mo of age. Conversely, infants who did not develop congenital T. cruzi infection had higher levels of IFN-γ than infected infants born to uninfected mothers. Monokine induced by IFN-γ, MCP-1, and IFN-γ production induced in T. cruzi-infected infants correlated with parasitemia, whereas the plasma levels of IL-17A, IL-17F, and IL-6 were less parasite load dependent. These findings support the existence of a distinct profile of cytokines and chemokines in the circulation of infants born to T. cruzi-infected mothers, which might predict congenital infection.
dc.formatpdf
dc.languageen
dc.publisherAmerican Association of Immunologists
dc.relationJournal of immunology (Baltimore, Md. : 1950)
dc.rightsopen
dc.sourceJournal of immunology 2016; 196(11):4596-602.
dc.subjectTrypanosoma Cruzi
dc.subjectEnfermedad de Chagas
dc.titleSerum Cytokines as Biomarkers of Early Trypanosoma cruzi infection by Congenital Exposure
dc.typeArtículo


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