| Literature DB >> 31358581 |
Ana Fernández-Villegas1, Elena Pérez-Antón1, Inmaculada Gómez1, Adriana Egui1, M Carmen Thomas2, Bartolomé Carrilero3, Ángel Del Pozo4, Maialen Ceballos5, Eduardo Andrés-León1, Miguel Ángel López-Ruz6, Eusebio Gainza4, Enrique Oquiñena5, Manuel Segovia3, Manuel Carlos López2.
Abstract
One of the current greatest challenges of Chagas disease is the establishment of biomarkers to assess the efficacy of drugs in a short period of time. In this context, the reactivity of sera from 66 adults with chronic indeterminate Chagas disease (IND) for a set of four Trypanosoma cruzi antigens (KMP11, PFR2, HSP70, and 3973d) was analyzed before and after benznidazole treatment. The results showed that the reactivity against these antigens decreased at 9, 24, and 48 months after treatment. Moreover, the 42.4% and 68.75% of IND patients met the established standard criteria of therapeutic efficacy (STEC) at 24 and 48 months posttreatment, respectively. Meeting the STEC implied that there was a continuous decrease in the reactivity of the patient sera against the four antigens after treatment and that there was a substantial decrease in the reactivity for at least two of the antigens. This important decrease in reactivity may be associated with a drastic reduction in the parasite load, but it is not necessarily associated with a parasitological cure. After treatment, a positive PCR result was only obtained in patients who did not meet the STEC. The percentage of granzyme B+/perforin+ CD8+ T cells was significantly higher in patients who met the STEC than in those who did not meet the STEC (35.2% versus 2.2%; P < 0.05). Furthermore, the patients who met the STEC exhibited an increased quality of the multifunctional response of the antigen-specific CD8+ T cells compared with that in the patients who did not meet the STEC.Entities:
Keywords: Chagas disease; Trypanosoma cruzi; antibodies; benznidazole; biomarkers; cellular response; cytokines; cytotoxic molecules; seroconversion; therapeutic response
Year: 2019 PMID: 31358581 PMCID: PMC6761566 DOI: 10.1128/AAC.02436-18
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191