| Literature DB >> 12405158 |
Barbara Lotti1, Thomas Wendland, Hansjakob Furrer, Nikhil Yawalkar, Salome von Greyerz, Karin Schnyder, Marlène Brandes, Pietro Vernazza, Ralf Wagner, Thi Nguyen, Eric Rosenberg, Werner J Pichler, Christian Brander.
Abstract
CD4+ T-helper cells appear to be essential in sustaining immune responses in chronic viral infections, as the maintenance of CD8+ cytotoxic T-lymphocyte responses and the control of viremia were demonstrated to depend on CD4+ T cell help. In order to investigate the function of HIV-specific CD4+ T cells in chronic HIV-1-infection, 49 chronically HIV-infected patients were analyzed before and 3 and 6 months after initiation of antiviral treatment. Ten patients showed a substantial, although weak, proliferative response to HIV-1-p55gag protein for which no improvement was observed upon initiation of HAART. From one individual, HIV-1-p55gag-specific CD4-positive T-cell clones were generated that were heterogeneous in their TCR Vbeta gene usage and HLA-DRB1*13 and DRB1*03 restricted, respectively. In addition, some CD4+ TCC produced substantial amounts of IFN-gamma and MIP-1alpha/beta were perforin-positive, and showed cytotoxic activity. These diverse functional features of HIV-specific CD4+ T cells suggest that they may exert direct antiviral activity.Entities:
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Year: 2002 PMID: 12405158 DOI: 10.1023/a:1020066404226
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317