Sm. Riordan et al., Serum immunoglobulin and soluble IL-2 receptor levels in small intestinal overgrowth with indigenous gut flora, DIG DIS SCI, 44(5), 1999, pp. 939-944
Murine studies have demonstrated that the presence of indigenous gut flora
is crucial for the induction of systemic immune hyporesponsiveness to antig
ens initially encountered within the gastrointestinal lumen. This study inv
estigated whether increased titers of such flora, as occur in human small i
ntestinal bacterial overgrowth, may be associated with increased suppressio
n of systemic immune responsiveness and the possible relation between syste
mic and mucosal immunity in this setting. Serum total immunoglobulin (Ig),
immunoglobulin subclass, and soluble interleukin-2 receptor levels and lami
na propria IgA plasma cell counts were determined in 50 consecutive subject
s with (N = 30) and without (N = 20) small intestinal bacterial overgrowth.
Luminal IgA levels were measured in 35 of these subjects. Serum concentrat
ions of IgG(3), but not of other immunoglobulin isotypes or soluble interle
ukin-2 receptors, were significantly reduced in subjects with bacterial ove
rgrowth (P < 0.0005). Small intestinal lamina propria IgA plasma cell count
s (P < 0.0005) and luminal IgA concentrations (P = 0.001) were significantl
y increased in this group. Serum IgG, levels were significantly inversely c
orrelated with luminal IgA levels (P < 0.01) and fell below the lower limit
of normal (0.41 g/liter) in 17/30 (56.7%) subjects with bacterial overgrow
th compared to 1/20 (5.0%) subjects without (P < 0.0005). These findings do
cument an association between small intestinal bacterial overgrowth with in
digenous gut flora and reduced serum IgG, reactivity in humans, possibly vi
a an interaction with mucosa-related immunoregulatory mechanisms. The possi
bility of underlying small intestinal bacterial overgrowth should be consid
ered in patients with serum IgG(3) deficiency, especially those with compat
ible symptoms and/or known predisposition.