Related Experiment Video
Updated: Dec 29, 2025

Sexual Transmission of American Trypanosomes from Males and Females to Naive Mates
Published on: January 27, 2019
Signaling pathways that regulate Trypanosoma cruzi infection and immune response
Fabio Marcelo Cerbán1, Cinthia Carolina Stempin1, Ximena Volpini2
1Universidad Nacional de Córdoba, Facultad de Ciencias Químicas, Departamento de Bioquímica Clínica, Córdoba, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Centro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI), Córdoba, Argentina.
Abstract:
Current understanding of key cellular pathways, which are activated by the interaction between T. cruzi and host immunity, is crucial for controlling T. cruzi infection and also for limiting the development of the immunopathological symptoms of Chagas´ disease. Here, we focus on recent advances in the knowledge of modulation of innate receptors such as TLRs and NLRs, especially NLRP3, by T. cruzi in different cells of the immune system. On the other hand, the modulation of macrophage activation may be instrumental in allowing parasite persistence and long-term host survival. In this sense, we discuss the importance of the metabolism of two amino acids: L-arginine and tryptophan, and evaluate the role of iNOS, arginase and IDO enzymes in the regulation of innate and adaptive immune response during this infection; and, finally, we also discuss how T. cruzi exploits the AhR, mTOR and Wnt signaling pathways to promote their intracellular replication in macrophages, thus evading the host's immune response.
Insights
Toxoplasma cruzi manipulates host immune cells by altering innate receptors and amino acid metabolism. Understanding these pathways is key to controlling Chagas disease and its symptoms.
Area of Science:
- Immunology
- Molecular Biology
- Parasitology
Background:
- Chagas disease, caused by Trypanosoma cruzi, presents complex immunopathology.
- Understanding host-parasite interactions is vital for disease control.
Purpose of the Study:
- To review recent advances in T. cruzi's modulation of host innate immunity.
- To explore parasite evasion strategies within macrophages.
Main Methods:
- Focus on Toll-like receptors (TLRs) and NOD-like receptors (NLRs), particularly NLRP3.
- Discussion of L-arginine and tryptophan metabolism via iNOS, arginase, and IDO.
- Analysis of T. cruzi exploitation of AhR, mTOR, and Wnt signaling pathways.
Main Results:
- T. cruzi modulates innate receptors like TLRs and NLRs (NLRP3) in immune cells.
- Macrophage activation is influenced by amino acid metabolism (L-arginine, tryptophan) and associated enzymes (iNOS, arginase, IDO).
- Parasite utilizes host signaling pathways (AhR, mTOR, Wnt) for intracellular replication and immune evasion.
Conclusions:
- T. cruzi actively manipulates host immune pathways for its survival and persistence.
- Targeting these modulated pathways offers potential therapeutic strategies for Chagas disease.
More Related Videos
13:21Establishment of Larval Zebrafish as an Animal Model to Investigate Trypanosoma cruzi Motility In Vivo
Published on: September 30, 2017
08:17Quantitative 3D Imaging of Trypanosoma cruzi-Infected Cells, Dormant Amastigotes, and T Cells in Intact Clarified Organs
Published on: June 23, 2022
Related Concept Videos
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
NF-κB-dependent Signaling Pathway
NF-κB-dependent Signaling Mechanism
The...
Inflammatory Response
Inflammation can be triggered by various stimuli, such as impact, abrasion, chemical irritation, infections, and extreme hot or cold temperatures. These can damage cells and connective tissue fibers,...
T Cell Types and Functions
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...