Effects of appendectomy and oral tolerance on dextran sulfate sodium colitis

AIM: To evaluate the concomitant effects of appendec- tomy and oral tolerance on colitis.METHODS: Delayed-type hypersensitivity (DTH) was investigated at a 7-d interval after ovalbumin (OVA) ad- ministration and immunization under normal and colitis conditions in appendectomized or sham-operated mic...

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Veröffentlicht in:World journal of gastroenterology : WJG 2011-05, Vol.17 (19), p.2437-2445
Hauptverfasser: Yue, Min, Shen, Zhe, Yu, Chao-Hui, Ye, Hua, Ye, Yue-Fang, Li, You-Ming
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Sprache:eng
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Zusammenfassung:AIM: To evaluate the concomitant effects of appendec- tomy and oral tolerance on colitis.METHODS: Delayed-type hypersensitivity (DTH) was investigated at a 7-d interval after ovalbumin (OVA) ad- ministration and immunization under normal and colitis conditions in appendectomized or sham-operated mice. Pathological scores for the colon were graded after in- gestion of colon-extracted protein (CEP) and induction of dextran sulfate sodium (DSS) colitis in appendecto- mized or sham-operated mice. Thereafter, Thl and Th2 in Peyer's patches and spleen lymphocytes were de- tected in CEP-treated and bovine serum albumin (BSA)-treated control mice.RESULTS: In appendectomized mice, DTH was not inhibited at day 7 after OVA administration and at the initial phase of DSS colitis, whereas it was inhibited at day 14 and day 21. However, in sham-operated mice, it was inhibited during the whole procedure and the onset of DSS colitis. The protective role of CEP against DSScolitis was present in sham-operated mice, with pre- dominant improvement of colonic pathological changes, while vanished in the appendectomized mice. A shift from Thl to Th2 in Peyer's patches resulted from a de- crease of Thl cells with the ingestion of CEP. Compared with BSA in the sham-operated group, no predominant changes were observed in the appendectomized mice.CONCLUSION: Appendectomy interferes with the pro- tective role of CEP in DSS colitis via a shift from Th2 to Thl during oral tolerance induction.
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v17.i19.2437