THE EXPRESSION OF COMPLEMENT PROTEIN-4 AND IGG3 IN LUMINAL SECRETIONS

Citation
Sm. Riordan et al., THE EXPRESSION OF COMPLEMENT PROTEIN-4 AND IGG3 IN LUMINAL SECRETIONS, Scandinavian journal of gastroenterology, 31(11), 1996, pp. 1098-1102
Citations number
25
Categorie Soggetti
Gastroenterology & Hepatology
ISSN journal
00365521
Volume
31
Issue
11
Year of publication
1996
Pages
1098 - 1102
Database
ISI
SICI code
0036-5521(1996)31:11<1098:TEOCPA>2.0.ZU;2-I
Abstract
Background: Factors regulating proximal small-intestinal luminal conce ntrations of IgG3, the predominant IgG subclass at this site, are uncl ear. This study determined whether luminal IgG3 concentrations are rel ated to those of complement protein 4 (C4), an acute-phase reactant pr edominantly derived from local mucosa. Methods: Proximal small-intesti nal luminal and peripheral blood Ige subclass and C4 concentrations we re measured by radial immunodiffusion in 30 adult subjects without pre disposition to disturbed mucosal immunity. Mucosal C4 immunoreactivity and the presence or absence of small-intestinal bacterial overgrowth were determined in all subjects. Caecal luminal concentrations of IgG3 and C4 were measured in a separate cohort of eight asymptomatic subje cts. Results: Proximal small-intestinal luminal C4 and IgG subclass co ncentrations were not significantly influenced by the presence or abse nce of small-intestinal bacterial overgrowth (P > 0.2). Nor did plasma C4 levels significantly influence C4 concentrations in small-intestin al luminal secretions (P > 0.2). Mucosal immunoreactivity for C4 was p resent in every subject. A significant correlation was found between C 4 and IgG3 concentrations in proximal smalt-intestinal luminal secreti ons (P < 0.0005) and also in caecal secretions (P < 0.05) but not in p eripheral brood (P > 0.1). Conclusions: Common factors, not including the presence or absence of small-intestinal bacterial overgrowth, regu late luminal concentrations of C4 and IgG3. Local investigation is man datory when assessing mucosal immune mechanisms.