The capacity of mucosal IgA Abs to serve as an excretory immune system in v
ivo was investigated. Mire expressing a transgenic TCR mere immunized intra
gastrically with the cognate Ag to elicit a vigorous mucosal IgA Ab respons
e. Soon after i.v. challenge, Ag was detected within the epithelial cells o
f the small intestinal crypts and to a lesser degree within the epithelial
cells higher up the villi, paralleling the gradient in expression of the po
lymeric Ig receptor and the transport of its ligand, oligomeric IgA. Uptake
of Ag into the epithelial cells occurred only from the basolateral aspect
and only when Ag complexed to IgA Ab could be present in the lamina propria
, The results support the concept that local IgA Abs can excrete Ags from t
he body by transporting them directly through mucosal epithelial cells, usi
ng the same mechanism that transports free IgA into the mucosal secretions.