Hat mitgewirkt an:
-
Murine cytomegalovirus induced T cell responses in the context of mucosal infection and as recombinant vectors
-
The viral context instructs the redundancy of costimulatory pathways in driving CD8+ T cell expansion
-
The mouse cytomegalovirus gene m42 targets surface expression of the protein tyrosine phosphatase CD45 in infected macrophages
-
Peptide processing is critical for T-Cell memory inflation and may be optimized to improve immune protection by CMV-based vaccine vectors