Bovine immunoglobulin concentrate Clostridium difficile retains C-difficile toxin neutralising activity after passage through the human stomach and small intestine

Citation
M. Warny et al., Bovine immunoglobulin concentrate Clostridium difficile retains C-difficile toxin neutralising activity after passage through the human stomach and small intestine, GUT, 44(2), 1999, pp. 212-217
Citations number
31
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
GUT
ISSN journal
00175749 → ACNP
Volume
44
Issue
2
Year of publication
1999
Pages
212 - 217
Database
ISI
SICI code
0017-5749(199902)44:2<212:BICCDR>2.0.ZU;2-V
Abstract
Background-Bovine immunoglobulin concentrate (BIC)-Clostridium difficile is prepared from the colostrum of cows immunised against C difficile toxins a nd contains high concentrations of neutralising IgG antitoxin. Aims-To determine the proportion of BIC-C difficile which survives passage through the human stomach and small intestine. Methods-Six volunteers with an end ileostomy took 5 g of BIC-C difficile co ntaining 2.1 g of bovine IgG on four occasions: alone, with an antacid, dur ing treatment with omeprazole, and within enteric coated capsules. Results-When BIC-C difficile was taken alone, a mean (SEM) of 1033 (232) mg of bovine IgG was recovered in the ileal fluid representing 49% of the tot al ingested dose. Bovine IgG recovery was not significantly increased by an tacid (636 (129) mg) or omeprazole (1052 (268) mg). The enteric capsules fr equently remained intact or only partially opened in the ileal effluent and free bovine IgG levels were low in this treatment group (89 (101) mg). Bov ine IgG recovery was higher in volunteers with shorter (less than two hours ) mouth to ileum transit times (68% versus 36%, p<0.05). Specific bovine Ig e against C difficile toxin A was detected in ileal fluid following oral BI G. Toxin neutralising activity was also present and correlated closely with bovine IgG levels (r=0.95, p<0.001). Conclusion-BIC-C difficile resists digestion in the human upper gastrointes tinal tract and specific anti-C difficile toxin A binding and neutralising activity was retained. Passive oral immunotherapy with anti-C difficile BIC may be a useful non-antibiotic approach to the prevention and treatment of C difficile antibiotic associated diarrhoea and colitis.