Skewed V<sub>β</sub> TCR repertoire of CD8<sup>+</sup> T cells in murine <i>Trypanosoma cruzi</i> infection

dc.contributor.authorMaria Leite‐de‐Moraes
dc.contributor.authorAntónio Coutinho
dc.contributor.authorMirellle Hontebeyrle-Joskowicz
dc.contributor.authorPaola Minóprio
dc.contributor.authorHarvey Eisen
dc.contributor.authorAntónio Bandeira
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T15:40:53Z
dc.date.available2026-03-22T15:40:53Z
dc.date.issued1994
dc.descriptionCitaciones: 24
dc.description.abstractWe have followed CD4 and CD8 TCR V beta repertoires during the acute phase of Trypanosoma cruzi infection in a resistant mouse strain (C57BL/6). No major changes were found in the V beta TCR distributions analyzed (covering roughly 40% of the TCR repertoire) in peripheral CD4 T lymphocytes, confirming the polyclonal nature of CD4 T cell responses. In contrast, in most animals, an over-representation of V beta 5 and V beta 14 TCR families was disclosed in the CD8 T cell compartment, superimposed on a predominantly polyclonal response. The preferential expansion of V beta 5+CD8+ T cells was also observed after infection of sensitive (C3H/HeJ, BALB/c) mouse strains. These observations suggest the existence of CD8 T cell-directed superantigenic activities associated with parasites.
dc.identifier.doi10.1093/intimm/6.3.387
dc.identifier.urihttps://doi.org/10.1093/intimm/6.3.387
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/53786
dc.language.isoen
dc.publisherOxford University Press
dc.relation.ispartofInternational Immunology
dc.sourceInstitut Pasteur
dc.subjectT-cell receptor
dc.subjectCD8
dc.subjectTrypanosoma cruzi
dc.subjectPolyclonal antibodies
dc.subjectBiology
dc.subjectT cell
dc.subjectBETA (programming language)
dc.subjectMolecular biology
dc.subjectT lymphocyte
dc.subjectVirology
dc.titleSkewed V<sub>β</sub> TCR repertoire of CD8<sup>+</sup> T cells in murine <i>Trypanosoma cruzi</i> infection
dc.typearticle

Files