Background: Mutations in the nucleotide oligomerization domain-2 (NOD2) gene and positive antibodies to microbial antigens have been found to be associated with the Crohn's disease (CD) phenotype, fibrostenosis. The aim of this study was to confirm these relationships in a large cohort of CD patient
Enhanced CBir1-specific innate and adaptive immune responses in Crohn's disease
β Scribed by Chong Shen; Carol J. Landers; Carrie Derkowski; Charles O. Elson; Stephan R. Targan
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 402 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1078-0998
No coin nor oath required. For personal study only.
β¦ Synopsis
Background: CBir1 is a dominant antigen with a role in innate and adaptive immunity in mouse models of colitis and antibodies to CBir1 are associated with severe human Crohn's disease (CD). Our aim was to determine whether CBir1 stimulates innate and antigen-specific T-cell responses in CD. We demonstrate that CBir1 enhanced IL-6 and IL-1β€ production by peripheral blood (PB) monocytes.
Methods:
Real time polymerase chain reaction (PCR) was used for measurement of IL6 and IL1 expression. [ 3 H] thymidine was used to measure T cell proliferation and Elispot assay was used to measure IFNβ₯ production.
Results: IL-6 was significantly increased in monocytes from CD compared to controls and ulcerative colitis (UC). Anti-CBir1 Ο© patients and IL-6 was inversely correlated. A significant increase in CBir1-specific peripheral T-cell proliferation was more evident in cells from CD than controls and UC. CBir1 induced increased numbers of IFN-gamma Ο© cells in lamina propria mononuclear cells (LPMC) from CD compared to UC and controls.
Conclusions: CBir1 induces enhanced peripheral innate and peripheral and mucosal antigen-specific T-cell responses in CD. Consistent with results from the mouse, CBir1 immune activation could play a role in CD.
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