The essential protective structure against the heavy enteric antigenic
burden, the gut mucosa, prevents penetration of noxious agents, but a
llows a minimal exchange of large molecules and particles between the
gut lumen and the 'milieu interieur' of the body. M cells in the folli
cle-associated epithelium of the gut, ideal gateways for the presentat
ion of enteric antigens to the cells of the gut-associated lymphoid ti
ssue (GALT), are also weak links in the mucosal barrier, and may provi
de access for various microorganisms. The afferent limb of the GALT co
nsists of distinct aggregates of lymphoid cells located in Peyer's pat
ches, the vermiform appendix and the solitary lymphatic follicles, and
of the mesenteric lymph nodes. The efferent limb subsumes the diffuse
ly scattered mucosal leukocytes, mainly lymphocytes and plasma cells.
Intraepithelial and mucosal T lymphocytes are instrumental in launchin
g local immune responses, producing lymphokines, and in the specific l
ysis of virally infected cells. Antigenic stimulation of the GALT resu
lts in local secretion of antibodies, or in suppression of systemic im
munologic responses to ingested antigens ('oral tolerance'). Poorly co
ntrolled mucosal immune responses result in organ-specific diseases. E
xtranodal lymphomas that mimic structures of the GALT may arise on a b
ackground of inflammatory or immunologic (autoimmune) disorders.