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Modulation of monocyte-derived dendritic cell antigen presentation using different HIV antigenic: potential use in therapeutic vaccine.

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Author(s):
Guilherme Gomes Silveira
Total Authors: 1
Document type: Master's Dissertation
Press: São Paulo.
Institution: Universidade de São Paulo (USP). Instituto de Ciências Biomédicas (ICB/SDI)
Defense date:
Examining board members:
Gil Benard; Jose Alexandre Marzagao Barbuto; Jorge Simão do Rosário Casseb
Advisor: Gil Benard
Abstract

Despite more than 20 years of effort, the design of an effective HIV-1 vaccine remains an enormous challenge. In this scenario, new immunological approaches must be considered. Monocytes from HIV-serodiscordant couples and non HIV exposed controls were differentiated in vitro into dendritic cells (MoDC), pulsed with different virus antigens and cultured with autologous lymphocytes. The T lymphocyte immunological response and the MoDC phenotype and function were determined. MoDCs were shown to be fully matured and activated in all antigen-pulsing protocols. Lymphocytes stimulated by DC pulsed with inactivated HIV or p55Gag protein showed greater activation, proliferation and IFN<font face=\"Symbol\">&#947 production in comparison to those stimulated by non pulsed MoDC. Nonetheless, T cells from non-exposed controls elicited the same response, except for the IFN<font face=\"Symbol\">&#947 production. This MoDC vaccine model may represent a viable and promising alternative of therapeutic vaccination against HIV. (AU)