MASKED DEFICIENCY OF C4 COMPONENT OF COMPLEMENT IN PATIENT S WITH CHRONIC GASTROINTESTINAL TRACT DISEASES OF DIFFERENT ETIOLOGY

Aim. Frequency of occurrence detection of C4A and C4B complement system deficiency in patients with chronic gastrointestinal tract (GIT) diseases including gastric ulcer (GU) and duodenal ulcer (DU). Materials and methods. 74 patients with chronic GIT diseases were examined. Endoscopy with stomach mucosa condition evaluation based on histobacterio- scopic examination of gastroduodenal biopsy samples was used. Intestine microbiocenosis evaluation was performed by using microflora degree of manifestation according to Federal Standard of Russian Ministry of Health № 231 —91500.11.0004-2003. C4A and C4B isotypes in blood sera of patients were measured by using enzyme immunoassay. Results. Chronic gastroduodenitis was diagnosed in 35.1%, pangastritis B — in 41.9%, GU and DU — in 23% of patients. Histological evaluation of biopsy samples revealed marked inflammatory changes in stomach and duodenum mucosa in 77% of patients. Stomach mucosa infec- tion rate by Helicobacter pylori reached 85%. Microbiological disorders manifestation in microflora of patients matched endoscopic and histobacteriscopic changes in it and was the highest for GU and DU. In 76.0% of cases C4A and C4B isotype deficiency in blood sera matches the development of erosive-ulcerous process in stomach and duodenum mucosa with marked background dysbiotic GIT microbiota disorders. Conclusion. Patients with functional deficiency of C4A and C4B isotypes have a genetic burden to susceptibility to chronic GIT diseases whereas H.pylori infection deteriorate the disease

Helicobacter pylori, complement system, enzyme immu- noassay, C4A, C4B isotypes, gastrointestinal tract, ulcer, Helicobacter pylori, intestine microflora