Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/1451
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dc.contributor.authorArgüello, Rafael Jen_US
dc.contributor.authorVigliano, Carlosen_US
dc.contributor.authorCabeza-Meckert, Patriciaen_US
dc.contributor.authorViotti, Rodolfoen_US
dc.contributor.authorGarelli, Fernandoen_US
dc.contributor.authorFavaloro, Liliana Een_US
dc.contributor.authorFavaloro, Roberto Ren_US
dc.contributor.authorLaguens, Rubénen_US
dc.contributor.authorLaucella, Susana A.en_US
dc.date.accessioned2019-12-05T19:15:39Z-
dc.date.available2019-12-05T19:15:39Z-
dc.date.issued2014-08-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/1451-
dc.description.abstractThe main consequence of chronic Trypanosoma cruzi infection is the development of myocarditis in approximately 20-30% of infected individuals but not until 10-20 years after the initial infection. We have previously shown that circulating interferon-γ-secreting T cells responsive to Trypanosoma cruzi antigens in chronic Chagas disease patients display a low grade of differentiation and the frequency of these T lymphocytes decreases along with the severity of heart disease. This study thought to explore the expression of inhibitory receptors, transcription factors of type 1 or regulatory T cells, and markers of T cell differentiation, immunosenescence or active cell cycle in cardiac explants from patients with advanced Chagas disease myocarditis.en_US
dc.language.isoenen_US
dc.relation.ispartofPLoS neglected tropical diseasesen_US
dc.titlePresence of antigen-experienced T cells with low grade of differentiation and proliferative potential in chronic Chagas disease myocarditisen_US
dc.typeArtículoen_US
dc.identifier.doi10.1371/journal.pntd.0002989-
item.openairetypeArtículo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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