The oral and pharyngeal mucosa is an active, immunological microenvironment quite different from other mucosal surfaces between the body and the external environment, such as the gastrointestinal mucosa. It has scant mucous coat and is covered by a thick stratified squamous epithelial cell layer, which expresses neither cell adhesion molecules nor class II MHC antigens. Thus, it has been speculated that the defense mechanism in the oral cavity and pharynx depends mainly on a nonimmunological mechanism which resists mechanical stimuli. Recently, however, squamous cells are identified as producers of a wide variety of cytokines in response to nonspecific stimulation in certain inflammatory diseases of the oral cavity and
in vitro experiments, and intraepithelial Langerhans cells have been in considered to be a unique subpopulation of antigenpresenting dendritic cells, which express class II MHC antigens and cell adhesion molecules such as ICAM-1 (CD54). The submucosal vascular unit, consisting of venule-like blood vessels, continuoresly expresses various cell adhesion molecules, including ICAM-1, E-selectin and P-selectin (CD62), regardless of the presence or absence of inflammatory infiltration. Cytokines released by squamous epithelial cells activated by external antigens upregulate the expression of these cell adhesion molecules. These events promote adhesion of circulating leucocytes, especially memory T cells and neutrophils, to the submucosal interstitium.
In contrast to the oral and pharyngeal mucosa, the intestinal mucosa is covered by a thick mucous coat containing immunoglobulins, such as secretory IgA (sIgA), which may con-tribute to the prevention of adhesion and uptake of microorganisms and dietary antigens in the intestinal tract, thereby forming a mucosal defense mechanism is its preferential utiliza-tion of IgA for its B cell response to antigenic challenge through the mucosa. The intestinal mucosa is equipped with a lymphoid apparatus consisting of organized lymphoid tissues, a diffuse collection of lymphocytes and plasma cells in the lamina propria and lymphocytes within villous epithelial cells which express class II MHC antigens whether or not inflamma-tion is present.
These findings indicate that microenvironmental diversity caused by differences of cover-ing epithelial cells leads changes in the pattern of mucosal defense mechanisms and immune-inflammatory responses.
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