Our goal is to develop a quantitative framework for the generation, boosting and maintenance of immunological memory. Mathematical models are useful because immunization and infection involve the interaction of rapidly changing populations of virus and multiple populations of immune cells. We first develop and validate models using experiments in mice. We then use these validated models to analyze data from human vaccination studies.
Aim 1 asks how prior immunity affects and potentially limit the boosting of immunity and apply this to influenza. Our approach is to develop models to understand why prior immunity limits boosting of antibodies to conserved regions of the virus. Specifically, we use our models to better understand how prior immunity might limit boosting of antibody responses to conserved regions on the stem of the hemagglutinin molecule that is the focus of universal influenza vaccines.
Aim 2 considers the factors that affect the durability of humoral immune memory, and address questions such as why memory generated by immunization with protein antigens is less durable than immunity generated by virus infection, and how prior immunity can differentially affect the boosting and generation of memory to new strains of influenza.
Aim 3 considers the generation of CD8 T cell memory to influenza and yellow fever. We will determine how repeated exposure to influenza affects the diversity of the CD8 T cell responses generated. We have access to a unique dataset that follows the number of YFV-specific CD8 T cells, changes in their phenotype, and their turnover from heavy water labelling studies for a period of over one year. Our analysis of this dataset will allow us to address an ongoing controversy regarding whether are long-term memory CD8 memory stem cells are generated rapidly after immunization or only gradually over time.
Aim 4 describes computational tools that we will build for B cell receptor sequence analysis and visualization, and for simulation of the dynamics of immune responses. These tools will be widely accessible online, and promoted at workshops and scientific symposia we organize.
Understanding the generation and maintenance of immunological memory is the foundation of effective vaccine development. We will contribute to this understanding by developing quantitative models for how immune responses are generated and boosted, and how immunological memory is maintained. This quantitative framework will help in the development of universal vaccines that provide broad protection against influenza. !
