Trypanosoma cruzi Experimental Infection Impacts on the Thymic Regulatory T Cell Compartment

dc.citation.titlePLOS Neglected Tropical Diseaseses
dc.creatorGonzález, Florencia Belén
dc.creatorCalmon-Hamaty, Flavia
dc.creatorCordeiro, Synara Nô Seara
dc.creatorFernández Bussy, Rodrigo
dc.creatorSpinelli, Silvana Virginia
dc.creatorD'Attilio, Luciano
dc.creatorBottasso, Oscar
dc.creatorSavino, Wilson
dc.creatorCotta-de-Almeida, Vinícius
dc.creatorRaquel Villar, Silvina
dc.creatorPérez, Ana Rosa
dc.date.accessioned2017-05-23T19:35:55Z
dc.date.available2017-05-23T19:35:55Z
dc.date.issued2016-01
dc.descriptionThe dynamics of regulatory T cells in the course of Trypanosoma cruzi infection is still debated. We previously demonstrated that acute murine T. cruzi infection results in an impaired peripheral CD4+Foxp3+ T cell differentiation due to the acquisition of an abnormal Th1-like phenotype and altered functional features, negatively impacting on the course of infection. Moreover, T. cruzi infection induces an intense thymic atrophy. As known, the thymus is the primary lymphoid organ in which thymic-derived regulatory T cells, known as tTregs, differentiate. Considering the lack of available data about the effect of T. cruzi infection upon tTregs, we examined tTreg dynamics during the course of disease. We confirmed that T. cruzi infection induces a marked loss of tTreg cell number associated to cell precursor exhaustion, partially avoided by glucocorticoid ablation- and IL-2 survival factor depletion. At the same time, tTregs accumulate within the CD4 single-positive compartment, exhibiting an increased Ki-67/Annexin V ratio compared to controls. Moreover, tTregs enhance after the infection the expression of signature markers (CD25, CD62L and GITR) and they also display alterations in the expression of migration-associated molecules (α chains of VLAs and chemokine receptors) such as functional fibronectin-driven migratory disturbance. Taken together, we provide data demonstrating profound alterations in tTreg compartment during acute murine T. cruzi infection, denoting that their homeostasis is significantly affected. The evident loss of tTreg cell number may compromise the composition of tTreg peripheral pool, and such sustained alteration over time may be partially related to the immune dysregulation observed in the chronic phase of the disease.es
dc.description.filFil: González, Florencia Belén. Instituto de Inmunología. Facultad de Ciencias Médicas (IDICER CONICET-UNR). Rosario; Argentinaes
dc.description.sponsorship: This work was supported by grants from ANPCyT-FONCyT PICT 2008-0980, EcosSUD A10S01 (Argentine), IOC/Fiocruz, Faperj and CNPq (Brazil) and Focem/Mercosures
dc.formatapplication/pdf
dc.format.extent1-21es
dc.identifier.issn1935-2735es
dc.identifier.urihttp://hdl.handle.net/2133/7385
dc.language.isoenges
dc.publisherPLoSes
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pntd.0004285es
dc.rightsopenAccesses
dc.rights.holder© 2016 González et al.es
dc.rights.texthttps://creativecommons.org/licenses/by/4.0/es
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectTrypanosoma cruzies
dc.subjectThymocyteses
dc.subjectThymuses
dc.titleTrypanosoma cruzi Experimental Infection Impacts on the Thymic Regulatory T Cell Compartmentes
dc.typearticle
dc.typeartículo
dc.typepublishedVersion
dc.type.collectionarticulo
dc.type.versionpublishedVersiones

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