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M. Susana Leguizamón

Researcher at University of Buenos Aires

Publications -  10
Citations -  545

M. Susana Leguizamón is an academic researcher from University of Buenos Aires. The author has contributed to research in topics: Trypanosoma cruzi & Sialic acid. The author has an hindex of 9, co-authored 10 publications receiving 523 citations.

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Thymocyte depletion in Trypanosoma cruzi infection is mediated by trans-sialidase-induced apoptosis on nurse cells complex

TL;DR: Supporting evidence is reported that TS is the virulence factor from T. cruzi responsible for the thymic alterations via apoptosis induction on the nurse cell complex, and that TS-neutralizing Abs elicitation during infection is associated with the reversion to thymi normal parameters.
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trans-Smlidase from Tvypanosoma cvuzi Induces Apoptosis in Cells from the Immune System In Vivo

TL;DR: In dose-response assays, apoptosis was observed even when an amount of trans-sialidase was administered that was enzymatically undetectable in blood, suggesting a role for sialic acid mobilization in T. cruzi-induced apoptosis of immune system cells.
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The trans-sialidase from Trypanosoma cruzi triggers apoptosis by target cell sialylation.

TL;DR: Lactitol, a competitive inhibitor that precluded the transference of the sialyl residue to endogenous acceptors but not the hydrolase activity of the enzyme, prevented ex vivo and in vivo the apoptosis caused by the trans‐sialidase.
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Evaluation of Brucella abortus Phosphoglucomutase (pgm) Mutant as a New Live Rough-Phenotype Vaccine

TL;DR: Vaccination with the Δpgm strain induced protection levels comparable to those induced by S19 and generated a proliferative splenocyte response and a cytokine profile typical of a Th1 response, while being unable to detect a specific anti-O-antigen antibody response by using the fluorescence polarization assay.
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Trypanosoma cruzi surface mucins with exposed variant epitopes.

TL;DR: It is shown that the hypervariable region is indeed present in the exposed mature N termini of the mucins because sera from infected hosts recognized peptides having sequences from this region.