Effect of infliximab on IFN-γ and IL-4 expression in peripheral blood and inflamed intestinal mucosa of patients with Crohn's disease

被引:0
|
作者
Ferkolj, Ivan
Markovic, Sasa
Veceric, Zeljka
Ihan, Alojz
Pohar, Maja
机构
[1] Univ Ljubljana, Ctr Med, Div Internal Med, Dept Gastroenterol, Ljubljana, Slovenia
[2] Univ Ljubljana, Fac Med, Inst Microbiol & Immunol, Ljubljana, Slovenia
[3] Univ Ljubljana, Fac Med, Inst Biomed Informat, Ljubljana, Slovenia
关键词
Crohn's disease; infliximab; interferon-gamma; interleukin-4;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Background: Infliximab, a monoclonal anti-tumor necrosis factor alpha (TNF-alpha) antibody, is an effective treatment for Crohn's disease without prior response to conventional therapy. It binds with high affinity to soluble and membrane-bound TNF-alpha, neutralizing its biological activity and reducing TNF-alpha production by mucosal cells. Its influence on other cytokines has been investigated to a much smaller extent. Aim: The aim of the study was to establish the influence of infliximab on cells containing the proinflammatory cytokine interferon-gamma (IFN-gamma) and the anti-inflammatory cytokine interleukin- 4 (IL-4) in peripheral blood and inflamed intestinal mucosa. Methods: Twenty-five patients with Crohn's disease (11 with the luminal and 14 with the fistular form) underwent treatment with infliximab. IFN-gamma and IL-4 containing cells in peripheral blood and inflamed intestinal mucosa were analysed by flow cytometry before and 14 days after the treatment. Results: Twenty-two patients (88%) showed a clinical response to the drug and three (12%) had no response. In the group of responders, the proportion of cells containing IFN-gamma and IL-4 in peripheral blood and inflamed intestinal mucosa remained unchanged after the treatment. Conclusions: Infliximab has no direct influence on cells containing IFN-gamma and IL-4 in peripheral blood and inflamed intestinal mucosa. The insignificant changes in the proportions of these cells observed after the treatment may be attributed to its direct effect on TNF-alpha, which resulted in silencing of the inflammation.
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页码:301 / 307
页数:7
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