I am a PhD candidate in the Immunology Program at the University of Chicago. My project is focused on characterizing the B cell response to influenza following vaccination with a universal influenza virus vaccine candidate. In my spare time, I enjoy painting to depict our laboratory’s scientific findings about how antibodies protect us from influenza virus.
Influenza HA-reactive antibodies
Influenza HA-reactive antibodies
Works on Paper
This image depicts epitopes on one of the major surface proteins on the influenza virus, hemagglutinin (HA). It highlights a paper published in the Journal of Virology: Vol 93, issue 21, in which the Wilson laboratory compared two types of current seasonal influenza vaccine: Flublok (a recombinant HA vaccine) and Flucelvax (a mammalian cell grown vaccine). The results show these two vaccines are similarly immunogenic but may differ in the preferences of the elicited antibodies toward the receptor-binding domain on the HA head (yellow-colored on the picture). The frequency of antibodies targeting conserved epitopes on the HA stalk domain (white-colored) was similar between both vaccines.
Phylogenetic trees of influenza viruses
Phylogenetic trees of influenza viruses
Works on Paper
This watercolor painting uses phylogenetic trees to depict the constant genetic changes of influenza viruses. Due to the limitations of current seasonal influenza virus vaccines, they typically elicit a strain-specific response and lose efficacy because of virus mutation in a process known as antigenic drift and shift. Scientists are developing a new generation of influenza vaccines that are able to induce antibodies with a broad protection and show high efficacy against homologous, drifted, and shifted influenza virus strains. “Antigenic drift” refers to small genetic changes, mostly in hemagglutinin (trimer, as shown in image), that lead to seasonal epidemics. It can be illustrated by the location of viruses close together on a phylogenetic tree. “Antigenic shift” indicates marked change in influenza A viruses where genomic segments are exchanged, resulting in a new influenza A subtype or a virus with a new hemagglutinin and/or neuraminidase (tetramer) combination.