9 research outputs found
Chagasic patients are able to respond against a viral antigen from influenza virus
<p>Abstract</p> <p>Background</p> <p><it>Trypanosoma cruzi,</it> the etiological agent of Chagasâ disease<it>,</it> is an obligate intracellular parasite which induces a CD8<sup>+</sup> T cell immune response with secretion of cytokines and release of cytotoxic granules. Although an immune-suppressive effect of <it>T. cruzi</it> on the acute phase of the disease has been described, little is known about the capacity of CD8<sup>+</sup> T cell from chronic chagasic patients to respond to a non-<it>T. cruzi</it> microbial antigen.</p> <p>Methods</p> <p>In the present paper, the frequency, phenotype and the functional activity of the CD8<sup>+</sup> T cells specific from Flu-MP*, an influenza virus epitope, were determined in 13 chagasic patients and 5 healthy donors.</p> <p>Results</p> <p>The results show that Flu-MP* peptide specific CD8<sup>+</sup> T cells were found with similar frequencies in both groups. In addition, Flu-MP* specific CD8<sup>+</sup> T cells were distributed in the early or intermediate/late differentiation stages without showing enrichment of a specific sub-population. The mentioned Flu-MP* specific CD8<sup>+</sup> T cells from chagasic patients were predominately T<sub>EM</sub> (CCR7- CD62L-), producing IL-2, IFNÎł, CD107a/b and perforin, and did not present significant differences when compared with those from healthy donors.</p> <p>Conclusions</p> <p>Our results support the hypothesis that there is no CD8<sup>+</sup> T cell nonspecific immune-suppression during chronic Chagas disease infection. Nonetheless, other viral antigens must be studied in order to confirm our findings.</p