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P012. The effects of faecal microbiota transplantation on the innate immune system and epithelial tight junction expression in chronic refractory pouchitis

J. Landy1, H. Omar Al-Hassi2, E. Ronde2, E. Mann2, S. Peake1, S. McLaughlin3, Z.L. Perry-Woodford4, P.J. Ciclitira5, R.J. Nicholls6, S.K. Clark7, S. Knight2, A.L. Hart1, 1St Mark's Hospital, IBD Unit, London, United Kingdom, 2Antigen Presentation Research Group, Imperial College, London, United Kingdom, 3Royal Bournemouth and Christchurch NHS Hospitals Trust, Gastroenterology, Bournemouth, United Kingdom, 4St Mark's Hospital, London, United Kingdom, 5St Thomas' Hospital, Gastroenterology, London, United Kingdom, 6Imperial College, Department of Biosurgery and Surgical Technology, London, United Kingdom, 7St Mark's Hospital, Colorectal Surgery, London, United Kingdom


Faecal microbiota transplantation (FMT) may be beneficial in IBD. A durable change in recipients' microbiota following FMT has been demonstrated. No previous study has assessed the immunological effects of FMT. We aimed to assess the immunological effects of FMT in patients with chronic refractory pouchitis.


FMT was performed via nasogastric tube within 6 hours of stool collection from a previously screened healthy donor. Mucosal biopsies samples were collected at pouchoscopy from eight patients with chronic refractory pouchitis before and four weeks after FMT. The epithelium was identified following incubation with EDTA and lamina propria dendritic cells (DCs) were identified following collagenase digestion. Epithelial cells were identified as pancytokeritin positive cells and expression of ZO-1, claudin 1 and claudin 2 were measured by multicolour flow cytometry. DC were identified as an HLA DR+, lineage (CD3, CD14, CD16, CD19, CD34) population. Expression of TLR 2, 4 and 5, β 7 and CCR 9, and CD40 were measured by multicolour flow cytometry. Cytokines were assessed by multiplex ELISA of biopsy supernatants. The t-test was used in statistical analysis.


There were no significant changes in epithelial expression of tight junctions. However, there was a tendency for increased expression of claudin 2 (18.6±11.4% v 39.6±13.4%, p = 0.3). Lower levels in lamina propria DC expression of TLR 4 (45.8±6.5% v 33.6±6.9%) and TLR 5 (35.5±12.2% v 23.3±11.5%) as well as β 7 expression (39.9±7.6% v 31.9±4.5%) were not statistically significant. There were no changes in the levels of IL2, 4, 6, 10, TNF, IFN or IL17 in the supernatant of mucosal biopsies before or 4 weeks after FMT. However, a rise in IL10 (9.1±1.2 pg/ml v 12.5±2.9 pg/ml, p = 0.2) was noted following FMT.


There were no significant alterations in epithelial tight junction expression or immunological factors studied following FMT. However, a non significant increase in the expression of “pore-forming” claudin 2 suggested a possible increase in paracellular transport of microbial signals to lamina propria DC with reduced expression of TLR 4 and 5 and of the gut homing marker β 7. This suggests that transplantation of healthy microbiota in chronic pouchitis might lead to a reduced microbial sensitivity of the lamina propria DC with increased IL10 production.