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- W1736123631 abstract "C rohn's disease is a chronic inflammatory bowel disease of unknown aetiology. Mucosal inflammatory dysregulation is likely important, with increased production of pro‐inflammatory cytokines, including tumour necrosis factor alpha ( TNF α). The chimeric monoclonal antibody, infliximab, inhibits TNF α and promotes intestinal mucosal healing. Despite this, many patients still require surgical intervention. Patients who have undergone colonic resection post‐infliximab therapy, show markedly variable morphological response to treatment. FOXP3 + CD4 + regulatory T ‐cells have been shown to have a protective role in autoimmune/inflammatory diseases and their sequestration to the bowel is found in those treated with infliximab. We examined the immunohistochemical profile of lymphoid aggregates in tissue sections from post‐infliximab C rohn's colitis resection specimens, classified as morphological responders or non‐responders, defined in relation to the absence/presence of mucosal ulceration and active inflammation, and a control group. Results indicated no significant diffences in CD68 ‐positive cell counts but increased FOXP3 ‐positive ( P = 0.02) and CD4 ‐positive ( P = 0.05) cell counts in responders versus non‐responders. Untreated control scores were similar to non‐responders. Although based on small study numbers, our results suggest an association between upregulation of FOXP3 +/ CD4 + regulatory T ‐cells and morphological response to infliximab therapy. This represents a possible quantitative methodology for monitoring therapeutic response to infliximab therapy, based on immunohistochemical evaluation of endoscopic biopsy specimens." @default.
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- W1736123631 date "2014-10-30" @default.
- W1736123631 modified "2023-10-09" @default.
- W1736123631 title "<scp>FOXP3</scp>+ regulatory <scp>T</scp>‐cell counts correlate with histological response in <scp>C</scp>rohn's colitis treated with infliximab" @default.
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- W1736123631 doi "https://doi.org/10.1111/pin.12219" @default.
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