Autoimmune diseases result from complex interactions among different T- and
B-lymphocyte subpopulations that target a rapidly growing number of autoan
tigens on different cell types. The etiology of most spontaneous autoimmune
disorders, and both the kinetics and hierarchy of the underlying autoimmun
e responses are poorly understood. However, important advances have been ma
de in recent years in our understanding of how autoreactive lymphocytes cau
se tissue damage, including the discovery that granzyme B binds to a cell s
urface receptor on target cells. This review is an attempt to summarize rec
ent developments in this area.