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1.
PLoS Negl Trop Dis ; 15(6): e0009473, 2021 06.
Artigo em Inglês | MEDLINE | ID: mdl-34061845

RESUMO

In chronic Chagas disease, Trypanosoma cruzi-specific T-cell function decreases over time, and alterations in the homeostatic IL-7/IL-7R axis are evident, consistent with a process of immune exhaustion. IL-27 is an important immunoregulatory cytokine that shares T-cell signaling with IL-7 and other cytokines of the IL-12 family and might be involved in the transcriptional regulation of T-cell function. Here, we evaluated the expression and function of IL-27R in antigen-experienced T cells from subjects with chronic Chagas disease and assessed whether in vitro treatment with IL-27 and IL-7 might improve T. cruzi-specific polyfunctional T-cell responses. In vitro exposure of PBMCs to T. cruzi induced a downregulation of IL-27R in CD4+ T cells and an upregulation in CD8+ T cells in subjects without heart disease, while IL-27R expression remained unaltered in subjects with more severe clinical stages. The modulation of IL-27R was associated with functional signaling through STAT3 and STAT5 and induction of the downstream genes TBX21, EOMES and CXCL9 in response to IL-27. In vitro treatment of PBMCs with IL-27 and IL-7 improved monofunctional and polyfunctional Th1 responses, accompanied by the induction of IL-10 and Bcl-2 expression in subjects without heart disease but did not improve those in subjects with cardiomyopathy. Our findings support the process of desensitization of the IL-27/IL-27R pathway along with disease severity and that the pro-inflammatory and immunomodulatory mechanisms of IL-27 might be interconnected.


Assuntos
Doença de Chagas/imunologia , Interleucina-27/imunologia , Adulto , Idoso , Linfócitos T CD8-Positivos/imunologia , Doença de Chagas/genética , Doença de Chagas/parasitologia , Doença Crônica , Feminino , Humanos , Interleucina-27/genética , Interleucina-7/genética , Interleucina-7/imunologia , Leucócitos Mononucleares/imunologia , Masculino , Pessoa de Meia-Idade , Receptores de Interleucina/genética , Receptores de Interleucina/imunologia , Fator de Transcrição STAT3/genética , Fator de Transcrição STAT3/imunologia , Trypanosoma cruzi/genética , Trypanosoma cruzi/fisiologia
2.
Methods Mol Biol ; 1955: 339-348, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30868539

RESUMO

Chagas disease is the highest impact parasitic disease in Latin America. In recent years, the use of immune-related biomarkers to predict diagnostic and treatment efficacy or to monitor diseases has been considered a promising tool. Our group has worked for the past 20 years on the characterization of different immunological aspects of the T-cell responses to T. cruzi antigens. We have shown that monitoring of appropriate immunological responses can provide earlier and robust measures of treatment.The Enzyme-Linked ImmunoSPOT (ELISPOT) assays are powerful tools to evaluate antigen-specific immune responses at the single-cell level. Herein, we describe uses of the ELISPOT assay to determine the T. cruzi-specific T-cell populations in PBMCs from chronic chagasic subjects.


Assuntos
Doença de Chagas/diagnóstico , Técnicas Imunoenzimáticas/métodos , Linfócitos T/imunologia , Trypanosoma cruzi/imunologia , Células Cultivadas , Doença de Chagas/tratamento farmacológico , Doença de Chagas/imunologia , Doença de Chagas/parasitologia , Doença Crônica , Humanos , Imunidade Celular , Leucócitos Mononucleares/imunologia , Leucócitos Mononucleares/parasitologia , Nitroimidazóis/farmacologia , Nitroimidazóis/uso terapêutico , Prognóstico , Linfócitos T/parasitologia , Resultado do Tratamento , Tripanossomicidas/farmacologia , Tripanossomicidas/uso terapêutico , Trypanosoma cruzi/efeitos dos fármacos
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