Inflammatory Bowel Diseases · 2016 · 15 citations · 31 references
Veterinary MedicineImmunologyInfectious DiseasesHost-pathogen InteractionsInflammationMucosal ImmunologyBacterial ToxinsGastrointestinal ImmunologyGastrointestinal InfectionsGastrointestinal InflammationHumoral ImmunityInflammatory Bowel DiseaseClostridium Perfringens InfectionColonic InflammationEnteric InflammationEnterotoxin-mediated DiseaseHost Immune Response MarkersInflammatory Bowel Disease ImmunopathogenesisInflammatory Bowel Disease PathophysiologySubjects
BACKGROUND: Clostridium difficile infection (CDI) affects patients with inflammatory bowel disease (IBD). The aim of this study was to compare humoral response to C. difficile toxins in IBD patients and control outpatients. METHODS: We prospectively followed adult IBD patients and control subjects with serum and stool samples obtained at enrollment and during periods of CDI and tested by PCR. Semiquantitative serum levels of IgM, IgG, and IgA to C. difficile toxins A and B were measured. RESULTS: Overall, 119 stool and 117 serum samples were obtained from 150 subjects. Different levels of IgA to toxin A (P = 0.0016) and toxin B (P = 0.0468) were noted between different IBD groups. Toxin A IgA levels were higher in the Crohn's disease group (P = 0.0321) and ileal pouch anal anastomosis (IPAA) group (P = 0.001) compared with the ulcerative colitis (UC) group, and toxin B IgA levels were higher in the IPAA group compared with the UC group (P = 0.0309). There were lower levels of toxin A IgA in IBD patients compared with those in subjects without new CDI (P = 0.0488) and higher levels in IBD patients with compared with those in subjects without CDI history before enrollment (P = 0.016). There were nonsignificant lower toxin A IgG levels in IBD patients compared with those in subjects without prior CDI (P = 0.095) and higher levels in control subjects with a history of CDI compared with IBD patients with prior CDI (P = 0.049). CONCLUSIONS: Patients with UC have lower IgA levels to C. difficile toxins compared with those with Crohn's disease and those after IPAA. Patients with IBD with prior CDI failed to demonstrate any increase in antitoxin IgG. Our findings suggest that IBD patients may benefit from immunization strategies targeting C. difficile toxins.
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Daniel N. Frank, Allison L. St. Amand, Robert A. Feldman et al. · Proceedings of the National Academy of Sciences · 2007 · 4.6K citations · Full text
Burden of <i>Clostridium difficile</i> Infection in the United States
Fernanda C. Lessa, Yi Mu, Wendy Bamberg et al. · New England Journal of Medicine · 2015 · 2.6K citations · Full text