Immunodominance in CD4 T Cell Responses
The defining feature of the immune system is its ability to distinguish self from non-self. The major component of the immune system responsible for this self / non-self discrimination is the diverse repertoire of antigen-specific T lymphocytes. T cell receptors can only recognize antigens derived from pathogens or transformed cells if these antigens in the derived peptide fragments of pathogenic protieins combine with Major Histocompatibility Complex (MHC) molecules.
The research in my laboratory centers around the molecular events that regulate MHC class II-restricted antigen presentation and CD4 T cell activation in vivo. Our long term goal is to make connections between the mechanisms involved in peptide acquisition by class II molecules and those aspects of immunology that critically depend on the specific peptides presented by the class II molecule and then to use this insight to enhance human vaccine design and evaluation.
Recent Publications
- (2012 May 01). The utility and limitations of current web-available algorithms to predict peptides recognized by CD4 T cells in response to pathogen infection. J Immunol. 188, 4235-48.
- (2011 Dec 01). Infection with seasonal influenza virus elicits CD4 T cells specific for genetically conserved epitopes that can be rapidly mobilized for protective immunity to pandemic H1N1 influenza virus. J Virol. 85, 13310-21.
- (2011 Jun 01). The memory phase of the CD4 T-cell response to influenza virus infection maintains its diverse antigen specificity. Immunology. 133, 246-56.





