Each T cell expresses unique T cell receptors (TCRs) on its surface which recognize a specific peptide fragment of an antigen, called epitopes, that are presented on the antigen presenting cell by human leukocyte antigen (HLA) molecules. HLA molecules are among the most complex molecules in our bodies and are highly diverse across populations. Class I HLA molecules present peptides from inside a cell and activate CD8+ T cells, allowing them to kill cancer cells, for example. Class II HLA molecules present antigens taken up from the outside of the cell, process them, and present them to CD4+ T cells. This activation of CD4+ T cells drives a number of cascading immune responses, including production of inflammatory cytokines and activation of B cells and macrophages.
The ability to identify all the components of the immune synapse represents one of the greatest opportunities for innovation in medical science and would allow us to create medicines that benefit patients across populations and with a variety of diseases. However, developing medicines based on an understanding of the immune synapse has been limited by its complexity, including the diversity of HLAs, the billions of potential epitopes they present, and the hundreds of millions of TCRs they can activate.