scholarly journals Trypanosoma cruziSSP4 Amastigote Protein Induces Expression of Immunoregulatory and Immunosuppressive Molecules in Peripheral Blood Mononuclear Cells

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Yadira Morán-Utrera ◽  
Aracely López-Monteon ◽  
José Luis Rosales-Encina ◽  
Enrique Méndez-Bolaina ◽  
Angel Ramos-Ligonio

The acute phase of Chagas' disease in mice and human is marked by states of immunosuppression, in whichTrypanosoma cruzireplicates extensively and releases immunomodulatory molecules that delay parasite-specific responses mediated by effector T cells. This mechanism of evasion allows the parasite to spread in the host. Parasite molecules that regulate the host immune response during Chagas’ disease have not been fully identified, particularly proteins of the amastigote stage. In this work, we evaluated the role of the GPI anchored SSP4 protein ofT. cruzias an immunomodulatory molecule in peripheral blood mononuclear cells (PBMCs). rMBP::SSP4 protein was able to stimulate nitric oxide (NO) production. Likewise, rMBP::SSP4 induced the expression of genes and production of molecules involved in the inflammatory process, such as, cytokines, chemokines, and adhesion molecules (CAMs) as determined by RT-PCR and ELISA. These results suggest that the amastigote SSP4 molecule could play a key role in the immunoregulatory and/or immunosuppressive process observed in the acute phase of infection withT. cruzi.

2016 ◽  
Vol 23 (5) ◽  
pp. 417-426 ◽  
Author(s):  
Federico Perdomo-Celis ◽  
Doris M. Salgado ◽  
Diana M. Castañeda ◽  
Carlos F. Narváez

ABSTRACTCryopreserved peripheral blood mononuclear cells (PBMCs) are widely used in studies of dengue. In this disease, elevated frequency of apoptotic PBMCs has been described, and molecules such as soluble tumor necrosis factor (TNF)-related apoptosis-inducing ligands (sTRAIL) are involved. This effect of dengue may affect the efficiency of PBMC cryopreservation. Here, we evaluate the viability (trypan blue dye exclusion and amine-reactive dye staining) and functionality (frequency of gamma interferon [IFN-γ]-producing T cells after polyclonal stimulation) of fresh and cryopreserved PBMCs from children with dengue (in acute and convalescence phases), children with other febrile illnesses, and healthy children as controls. Plasma sTRAIL levels were also evaluated. The frequencies of nonviable PBMCs detected by the two viability assays were positively correlated (r= 0.74;P< 0.0001). Cryopreservation particularly affected the PBMCs of children with dengue, who had a higher frequency of nonviable cells than healthy children and children with other febrile illnesses (P≤ 0.02), and PBMC viability levels were restored in the convalescent phase. In the acute phase, an increased frequency of CD3+CD8+amine-positive cells was found before cryopreservation (P= 0.01). Except for B cells in the acute phase, cryopreservation usually did not affect the relative frequencies of viable PBMC subpopulations. Dengue infection reduced the frequency of IFN-γ-producing CD3+cells after stimulation compared with healthy controls and convalescent-phase patients (P≤ 0.003), and plasma sTRAIL correlated with this decreased frequency in dengue (rho = −0.56;P= 0.01). Natural dengue infection in children can affect the viability and functionality of cryopreserved PBMCs.


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