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Field: Virology and Immunology Research Interest:
T lymphocytes have been reported to
play a major role in regulating other cell populations within the immune
system, while B cell functions have traditionally been associated to antibodies
production. We showed that B lymphocytes also display immune-modulatory
properties during parasitic infections, influencing T cells and macrophages
and more strikingly, controlling themselves. Thus, during Trypanosoma
cruzi (T. cruzi) infection- a chronic and transmissible disease also called
Chagas' disease- highly activated B cells increase the expression of galectin-1,
a beta-galactoside-binding protein. This lectin modulates both T cells
and infected macrophages citokyne secretion and survival, and displays
a biphasic influence on macrophages microbicidal activity. Moreover, we
proved that B cell apoptosis is an ongoing process in vivo during T. cruzi
infection, that it is B cell sufficient, and mediated by the Fas/FasL
pathway. Interestingly, our data indicate that FasL-mediated B cell fratricide
selectively eliminates IgG+ activated B cell reactive against parasite
antigens. Currently we are conducting experiments using bone marrow from
normal and T cruzi infected mice in order to evaluate whether B lymphocytes
are targets and/or effectors of central immune-regulatory mechanisms triggered
in the context of this infectious process. |
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