Volume 9 Supplement 2
Early presentation of HIV-1 KF11Gag and KK10Gag protective epitopes facilitate rapid CD8+ T cell activation and killing of virus infected cells
© Kløverpris et al; licensee BioMed Central Ltd. 2012
Published: 13 September 2012
CD8+ T cells are major players for the antiviral immunity against HIV-1 through recognition of viral epitopes presented on the surface of infected cells. However, the kinetics and timing of HIV-1 epitope presentation remains poorly understood but nonetheless crucial for development of a successful CD8+ T cell based vaccine.
Epitope presentation and killing of virus infected cells was assessed in HIV-1 susceptible T cell lines, H9, U937, primary CD4+, and B cell lines expressing HLA-B*5701 or B*2705 by synchronized infection with HIV-1 or VSV-HIV-1 to determined the contribution of incoming particles to epitope presentation. Infected cells were co-cultured with CD8+ T cell lines specific for the epitopes KF11Gag, KK10Gag, KY9Pol and VL9Vpr. Kinetics of epitope presentation were monitored by the production of CD107b and MiP1ß in the co-culture at 0, 3, 6, 18 and 24 hours post-infection. In addition, killing of infected cells was determined in paralleled by the decrease of CD4+/p24 Gag+ cells.
We comprehensively studied the kinetics of antigen presentation of the KF11Gag and KK10Gag epitopes, restricted by protective HLA alleles B*5701 and B*2705, and compared these to KY9Pol and VL9Vpr epitopes, in a single cycle of virus replication. We observed differences in epitope presentation kinetics with early presentation within 3 hours post-infection, for KF11Gag, KK10Gag and KY9Pol epitopes, but only late presentation for VL9Vpr. In addition, we illustrate how early presentation relies on antigen processing from incoming virus, which correlates with rapid CD8+ T cell activation and clearance of virus-infected cells.
Our data strongly support the importance of identifying early-presented HIV-1 epitopes to eliminate infected cells before the release of new infectious viral particles.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.