Exogenous antigens can impinge upon the luminal surface of mucous memb
ranes and to a limited degree, can even penetrate into the lamina prop
ria. As a result of infection, microbial antigens can be present in mu
cosal epithelium or lamina propria. ill all three levels (lumen, epith
elium, lamina propria), locally produced antibodies, principally immun
oglobulin A (IgA), can combine with antigens. As a result, antigens ca
n be prevented from attaching to the epithelium, viruses can be neutra
lized inside epithelial cells and immune complexes in the lamina propr
ia can be excreted into the lumen. As the Fc portion of IgA is special
ized to facilitate epithelial transport of IgA rather than to activate
inflammatory mediator systems (as is the case with other classes of i
mmunoglobulin), the predominance of IgA among mucosal antibodies serve
s to limit the degree of local inflammation following antigen-antibody
reactions.