The role of inhibitory receptors and their ligands in immune escape from CD8+ T cells and the establishment of chronic virus infection

• Antragsteller: Dr. Gennadiy Zelinskyy, seit 7/2015
• Fachliche Zuordnung: Virologie
• Förderung: Förderung von 2013 bis 2015
• Projektkennung: Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 229125353

CD8+ T cells are critical for the control of most virus infections but they cannot eliminate virus in chronic infections. Several studies imply that functional exhaustion of CD8+ T cells induced by inhibitory receptors is associated with chronic infection. However, we and others have recently shown that effector CD8+ T cells express high levels of inhibitory receptors during acute viral infections but are highly functional at this time point. These results indicate that inhibitory receptors are not necessarily associated with T cell exhaustion. We hypothesize that during acute infections with chronic viruses inhibitory receptor/ligand interaction might be more important for immune escape of virus-infected cells, which can then result in chronic infection. This is in line with our preliminary finding that Friend retrovirus-infected cells express high levels of inhibitory ligands during acute infection. We will use the Friend retrovirus model to define the mechanisms of immune escape by inhibitory receptors/ligands during the late phase of acute retroviral infection. In addition, we will block this interaction to prevent the establishment of viral chronicity.

• DFG-Verfahren: Sachbeihilfen
• Ehemalige Antragstellerin: Dr. Kirsten K. Dietze, bis 6/2015