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1.
Mem. Inst. Oswaldo Cruz ; 115: e200110, 2020. tab, graf
Article in English | LILACS, SES-SP | ID: biblio-1135276

ABSTRACT

We aimed to investigate the association of CD14 -260C/T (rs2569190) polymorphism and Chagas cardiomyopathy and the functional characteristics of CD14+ and CD14- monocytes upon infection with Trypanosoma cruzi. We observed an association between the T- genotype (absence of allele -260T) related to low CD14 expression and the dilated cardiomyopathy type of Chagas disease. Furthermore, we observed that CD14- monocytes showed a more activated profile upon in vitro infection with T. cruzi than CD14+ monocytes. Our findings suggest that T- genotype is associated with susceptibility to develop Chagas dilated cardiomyopathy, likely linked to the T. cruzi-induced inflammatory profile of CD14- monocytes.


Subject(s)
Humans , Cardiomyopathy, Dilated/genetics , Chagas Cardiomyopathy/genetics , Lipopolysaccharide Receptors/genetics , Trypanosoma cruzi , Chagas Disease , Ventricular Dysfunction, Left , Genotype , Heart Failure
2.
Mem. Inst. Oswaldo Cruz ; 104(supl.1): 208-218, July 2009. ilus
Article in English | LILACS | ID: lil-520881

ABSTRACT

Perhaps one of the most intriguing aspects of human Chagas disease is the complex network of events that underlie the generation of protective versus pathogenic immune responses during the chronic phase of the disease. While most individuals do not develop patent disease, a large percentage may develop severe forms that eventually lead to death. Although many efforts have been devoted to deciphering these mechanisms, there is still much to be learned before we can fully understand the pathogenesis of Chagas disease. It is clear that the host's immune response is decisive in this process. While characteristics of the parasite influence the immune response, it is becoming evident that the host genetic background plays a fundamental role in the establishment of pathogenic versus protective responses. The involvement of three complex organisms, host, parasite and vector, is certainly one of the key aspects that calls for multidisciplinary approaches towards the understanding of Chagas disease. We believe that now, one hundred years after the discovery of Chagas disease, it is imperative to continue with highly interactive research in order to elucidate the immune response associated with disease evolution, which will be essential in designing prophylactic or therapeutic interventions.


Subject(s)
Humans , Chagas Disease/parasitology , Trypanosoma cruzi , Acute Disease , Chronic Disease , Chagas Disease/immunology , Immunity, Cellular , Trypanosoma cruzi/genetics , Trypanosoma cruzi/immunology , Trypanosoma cruzi/pathogenicity
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