As part of the gut epithelial barrier, sIgA is important in the development of immune tolerance for normal, beneficial commensal gut organisms, as well as common molecular epitopes found in foods.
Early studies of sIgA focused on immune exclusion (the prevention of pathological material and organisms from gaining entry into the general circulation). Recent studies also show sIgA plays a role in immune inclusion (delivery of commensal bacteria and their products to the gut and systemic immune system) for recognition. This leads to the development of immune tolerance. Immune inclusion spares beneficial organisms from destruction by the immune system which helps to support the immune system in a noninflammatory way to preserve local homeostasis.
Although secretory IgA is the major antibody in the intestinal mucosa, the prevalence of GI disorders in patients with systemic IgA deficiency is not as high as one might expect. It is thought that the transportation of IgM from the mucosa can compensate for a lack of IgA.
In people with genetic immunodeficiency of systemic sIgA, GI symptoms such as diarrhea have been reported. Systemically IgA-deficient patients more often have airway infections since compensatory sIgM is lacking in the airways (in contrast to the gut). Adaptive sIgA responses may allow the host to respond to fluctuations in commensal bacteria to favor mucosal homeostasis.
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