| Literature DB >> 15246319 |
Gonzalo Peluffo1, Lucía Piacenza, Florencia Irigoín, María Noel Alvarez, Rafael Radi.
Abstract
Trypanosoma cruzi invades a diversity of nucleated cells in the mammalian host. Macrophages are among the first cells to be parasitized and, after activation by inflammatory stimuli, they participate in the control of infection. However, some parasites manage to evade the immune response and establish a chronic infection in differentiated cells. L-arginine is located at the crossroads of divergent routes that produce metabolites, including nitric oxide and polyamines, which influence the outcome (i.e. resolution or progression) of infection. This article discusses the fate and actions of L-arginine-derived biomolecules formed both in the host and in the parasite during T. cruzi-host-cell interactions.Entities:
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Year: 2004 PMID: 15246319 DOI: 10.1016/j.pt.2004.05.010
Source DB: PubMed Journal: Trends Parasitol ISSN: 1471-4922