Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/34826
Title: Pathogen-Induced Proapoptotic Phenotype and High CD95 (Fas) Expression Accompany a Suboptimal CD8(+) T-Cell Response: Reversal by Adenoviral Vaccine
Authors: Vasconcelos, Jose Ronnie Carvalho de [UNIFESP]
Bruna-Romero, Oscar
Araujo, Adriano F. [UNIFESP]
Dominguez, Mariana R. [UNIFESP]
Ersching, Jonatan [UNIFESP]
Alencar, Bruna C. G. de [UNIFESP]
Machado, Alexandre V.
Gazzinelli, Ricardo T.
Bortoluci, Karina R. [UNIFESP]
Amarante-Mendes, Gustavo P.
Lopes, Marcela F.
Rodrigues, Mauricio Martins [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Universidade Federal de Minas Gerais (UFMG)
Fiocruz MS
Univ Massachusetts
Universidade de São Paulo (USP)
Universidade Federal do Rio de Janeiro (UFRJ)
Issue Date: 1-May-2012
Publisher: Public Library Science
Citation: Plos Pathogens. San Francisco: Public Library Science, v. 8, n. 5, 16 p., 2012.
Abstract: MHC class la-restricted CD8(+) T cells are important mediators of the adaptive immune response against infections caused by intracellular microorganisms. Whereas antigen-specific effector CD8(+) T cells can clear infection caused by intracellular pathogens, in some circumstances, the immune response is suboptimal and the microorganisms survive, causing host death or chronic infection. Here, we explored the cellular and molecular mechanisms that could explain why CD8(+) T-cell-mediated immunity during infection with the human protozoan parasite Trypanosoma cruzi is not optimal. for that purpose, we compared the CD8(+) T-cell mediated immune responses in mice infected with T. cruzi or vaccinated with a recombinant adenovirus expressing an immunodominant parasite antigen. Several functional and phenotypic characteristics of specific CD8(+) T cells overlapped. Among few exceptions was an accelerated expansion of the immune response in adenoviral vaccinated mice when compared to infected ones. Also, there was an upregulated expression of the apoptotic-signaling receptor CD95 on the surface of specific T cells from infected mice, which was not observed in the case of adenoviral-vaccinated mice. Most importantly, adenoviral vaccine provided at the time of infection significantly reduced the upregulation of CD95 expression and the proapoptotic phenotype of pathogen-specific CD8(+) cells expanded during infection. in parallel, infected adenovirus-vaccinated mice had a stronger CD8(+) T-cell mediated immune response and survived an otherwise lethal infection. We concluded that a suboptimal CD8(+) T-cell response is associated with an upregulation of CD95 expression and a proapoptotic phenotype. Both can be blocked by adenoviral vaccination.
URI: http://repositorio.unifesp.br/handle/11600/34826
ISSN: 1553-7374
Other Identifiers: http://dx.doi.org/10.1371/journal.ppat.1002699
Appears in Collections:Em verificação - Geral

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