Olsen Trine, Cui Guanglin, Goll Rasmus, Husebekk Anne, Florholmen Jon
Laboratory of Gastroenterology, Institute of Clinical Medicine, University of Tromsø, Tromsø, Norway.
Scand J Gastroenterol. 2009;44(6):727-35. doi: 10.1080/00365520902803507.
The mechanisms of action of infliximab (IFX) in the treatment of ulcerative colitis (UC) are poorly understood. The aim of the study was to investigate the changes in tissue expression of tumor necrosis factor-alpha (TNF-alpha) and other cytokines in UC patients receiving IFX treatment.
The levels of TNF-alpha, interleukin (IL)-10, IL-4, and interferon-gamma (IFN-gamma) mRNA in colonic biopsies from 32 UC patients during IFX treatment were measured by real-time polymerase chain reaction (PCR) and compared with those of 19 controls. Immunohistochemistry was performed to characterize the changes of inflammatory cells during treatment.
IFX reduced the expression of TNF-alpha and IFN-gamma mRNA, but not that of IL-10 and IL-4 mRNA. Reductions in TNF-alpha mRNA were correlated to clinical and endoscopic improvements, and normalization of TNF-alpha mRNA was obtained in patients with healed mucosa. The numbers of T lymphocytes and macrophages were significantly decreased in patients with healed mucosa after IFX treatment, although compared to normal controls, there were still increased levels of TNF-alpha-positive cells after treatment.
IFX induced down-regulation of the mucosal TNF-alpha and IFN-gamma mRNA expression in UC patients. The numbers of T lymphocytes and macrophages were significantly decreased in patients with endoscopically healed mucosa after IFX treatment.
英夫利昔单抗(IFX)治疗溃疡性结肠炎(UC)的作用机制尚不清楚。本研究旨在调查接受IFX治疗的UC患者组织中肿瘤坏死因子-α(TNF-α)和其他细胞因子表达的变化。
采用实时聚合酶链反应(PCR)检测32例接受IFX治疗的UC患者结肠活检组织中TNF-α、白细胞介素(IL)-10、IL-4和干扰素-γ(IFN-γ)mRNA的水平,并与19例对照者进行比较。采用免疫组织化学方法观察治疗期间炎症细胞的变化。
IFX降低了TNF-α和IFN-γ mRNA的表达,但未降低IL-10和IL-4 mRNA的表达。TNF-α mRNA的降低与临床和内镜改善相关,黏膜愈合患者的TNF-α mRNA恢复正常。IFX治疗后黏膜愈合患者的T淋巴细胞和巨噬细胞数量显著减少,尽管与正常对照相比,治疗后TNF-α阳性细胞水平仍升高。
IFX可诱导UC患者黏膜TNF-α和IFN-γ mRNA表达下调。IFX治疗后内镜下黏膜愈合患者的T淋巴细胞和巨噬细胞数量显著减少。