Th-17 cytokines are associated with severity of Trypanosoma cruzi chronic infection in pediatric patients from endemic areas of Mexico
Por:
De Alba-Alvarado, Mariana, Maria Salazar-Schettino, Paz, Jimenez-Alvarez, Luis, Cabrera-Bravo, Margarita, Garcia-Sancho, Cecilia, Zenteno, Edgar, Vazquez-Antona, Clara, Cruz-Lagunas, Alfredo, Zuniga, Joaquin, Irene Bucio-Torres, Martha
Publicada:
1 feb 2018
Resumen:
In Chagas disease the clinical, acute and chronic manifestations are the result of the interaction between the parasite and the host factors. The balance between inflammatory and anti-inflammatory immune responses is essential for the increase or resolution of the manifestations in individuals infected with T. cruzi. To identify if children with chronic Chagas disease and heart injury is related with non-regulated Th1, Th2 and Th17 responses. We included 31 children with T. cruzi confirmed chronic infection from endemic areas of Mexico. Subsequently, they were separated according to their ECHO and ECG results into three groups according to the severity of cardiac involvement. Circulating Th1, Th2 and Th17 cytokine profiles were performed by Luminex assays and the results were analyzed by bivariate and multivariable analysis. Patients were classified in asymptomatic chronic (group 1, N = 12); individuals with IRBBB in ECG and incipient lesions in ECHO (Group 2, N = 8) and Patients with severe chronic symptomatic disease (Group 3, N = 11). The analysis of immune mediators revealed that patients with severe cardiac manifestations had significant higher levels (p < 0.05) of Th17 related cytokines including IL-17 and IL-6 as well as IFN-? and IL-2. Also patients with severe cardiomyopathy exhibit increased levels of IL-13 (p < 0.05) after multivariate analysis. High levels of Th17 related cytokines including IL-17, IFN-?, IL-6 and IL-2 and pro-fibrotic factors such as IL-13 could be associated to the severity of cardiac involvement in children with chronic T. cruzi infection. These cytokines could be useful as indicators for the early identification of cardiac damage associated to the T. cruzi infection. © 2017
Filiaciones:
Univ Nacl Autonoma Mexico, Fac Med, Dept Microbiol & Parasitol, Edificio A,2 Piso,Ciudad Univ,Circuito Escolar, Mexico City 04510, DF, Mexico
Inst Nacl Enfermedades Resp Ismael Cosio, Lab Inununobiol & Genet, Mexico City, DF, Mexico
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