Literature DB >> 19854145

Benznidazole alters the pattern of Cyclophosphamide-induced reactivation in experimental Trypanosoma cruzi-dependent lineage infection.

Daniela M Santos1, Tassiane A F Martins, Ivo S Caldas, Lívis F Diniz, George L L Machado-Coelho, Cláudia M Carneiro, Riva de P Oliveira, André Talvani, Marta Lana, Maria T Bahia.   

Abstract

The factors involved in the reactivation of chronic Chagas disease infection are not clear enough and may be related to host immune unbalance and/or parasite genetic diversity. To evaluate the role of the Trypanosoma cruzi genetic background in the Chagas disease reactivation, we inoculated Cyclophosphamide-immunosupressed (CyI) Swiss mice with clonal stocks from T. cruzi I (Cuica cl1, P209 cl1, Gamba cl1, SP104 cl1), T. cruzi II (IVV cl4, MVB cl8) and T. cruzi (Bug2148 cl1, MN cl2) lineages. We used the parasitemia as the parameter for Chagas disease reactivation and observed that CyI animals infected with T. cruzi stocks showed no reactivation and those infected with T. cruzi II stocks showed only 5% of reactivation. In contrast, immunosuppressed mice infected with stocks from T. cruzi I lineage showed 77.5 and 51.25% reactivation of the infection when Cyclophosphamide treatment was performed 60 and 180 days after inoculation, respectively. Next, we evaluated the efficacy of the Benznidazole (Bz) pre-treatment in reducing or preventing the recurrence of the infection in these CyI animals. In general, the percentage of the parasite recurrence was not altered among the CyI mice that received the Bz pre-treatment during the acute phase of the infection. Interestingly, when pre-Bz treatment was performed during the chronic phase, we observed two different patterns of response: (i) an increased protection among the animals inoculated with the SP104 cl1 (genotype 19) and Cuica cl1 (genotype 20) stocks; (ii) an increased percentage of parasitemia reactivation among mice inoculated with Gamba cl1 (genotype 19) and P209 cl1 (genotype 20) T. cruzi stocks. Our results corroborate our hypothesis by showing that the T. cruzi genetic background in combination with specific Bz treatment has an important role in the Chagas disease reactivation in immunosuppressed animals. Copyright 2009 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19854145     DOI: 10.1016/j.actatropica.2009.10.007

Source DB:  PubMed          Journal:  Acta Trop        ISSN: 0001-706X            Impact factor:   3.112


  4 in total

1.  Mice Intragastric Infected with Insect and Blood Trypomastigotes of Trypanosoma cruzi IV: Differences and Similarities on the Evolution Profile and Response to Etiological Treatment.

Authors:  Miyoko Massago; Gerson Zanusso Junior; Elaine Schultz Dworak; Elisama Loubak da Silva; Alexandre Tadachi Morey; Mônica Lúcia Gomes; Max Jean de Ornelas Toledo
Journal:  Acta Parasitol       Date:  2021-04-23       Impact factor: 1.440

2.  Nutritional Status Driving Infection by Trypanosoma cruzi: Lessons from Experimental Animals.

Authors:  Guilherme Malafaia; André Talvani
Journal:  J Trop Med       Date:  2011-04-14

3.  Incomplete Recruitment of Protective T Cells Is Associated with Trypanosoma cruzi Persistence in the Mouse Colon.

Authors:  Alexander I Ward; Michael D Lewis; Martin C Taylor; John M Kelly
Journal:  Infect Immun       Date:  2021-11-15       Impact factor: 3.441

4.  Library of Selenocyanate and Diselenide Derivatives as In Vivo Antichagasic Compounds Targeting Trypanosoma cruzi Mitochondrion.

Authors:  Rubén Martín-Escolano; Daniel Molina-Carreño; Daniel Plano; Socorro Espuelas; María J Rosales; Esther Moreno; Carlos Aydillo; Carmen Sanmartín; Manuel Sánchez-Moreno; Clotilde Marín
Journal:  Pharmaceuticals (Basel)       Date:  2021-05-01
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.