Helper T cell-regulated B cell responses constitute a major component of th
e primary immune response to many pathogens. The subsequent development of
antigen-specific immune memory is one critical outcome of this primary adap
tive immune response. Antigen-specific immunity develops through a series o
f intercellular information exchanges organized around cognate T cell recep
torpeptide/MHC interactions. Here, we discuss these complex molecular event
s and their cellular consequences in a serial synapsis model of adaptive im
munity. Our laboratory has developed strategies to isolate antigen-specific
Th cells and B cells to analyze gene expression and cellular function in s
ingle responding lymphocytes directly ex vivo. These studies provide insigh
t into the regulation and cellular organization of antigen-specific immune
responses in vivo.