Plasma cells are cellular factories devoted entirely to the manufacture and
export of a single product: soluble immunoglobulin (Ig). As the final medi
ators of a humoral response, plasma cells play a critical role in adaptive
immunity. Although intense effort has been devoted to studying the regulati
on and requirements for early B cell development, little information has be
en available on plasma cells. However, more recent work-including studies o
n genetically altered mice and data from microarray analyses-has begun to i
dentify the regulatory cascades that initiate and maintain the plasma cell
phenotype. This review will summarize our current understanding of the mole
cules that regulate commitment to a plasma cell fate and those that mediate
plasma cell function.