Baert F J, D'Haens G R, Peeters M, Hiele M I, Schaible T F, Shealy D, Geboes K, Rutgeerts P J
Department of Gastroenterology, University Hospital Gasthuisberg, Leuven, Belgium.
Gastroenterology. 1999 Jan;116(1):22-8. doi: 10.1016/s0016-5085(99)70224-6.
BACKGROUND & AIMS: Anti-tumor necrosis factor alpha monoclonal antibody treatment (infliximab) reduces clinical signs and symptoms in patients with Crohn's disease. The effects of infliximab on mucosal histopathologic abnormalities in Crohn's ileocolitis were studied.
Thirteen patients with steroid-refractory Crohn's disease were treated with a single infusion of infliximab (5-20 mg/kg), and 5 were treated with placebo. Ileal and colonic biopsy specimens of all patients were collected before and 4 weeks after therapy. Severity of inflammation was assessed by a histological score. Immunohistochemical stainings with antibodies against HLA-DR, CD68, tumor necrosis factor alpha, intercellular adhesion molecule 1, lymphocyte function-associated antigen, CD4, CD8, and interleukin 4 were performed.
Total histological activity score was reduced significantly in both ileitis and colitis after infliximab. This is caused by a virtual disappearance of the neutrophils and a reduction of mononuclear cells. Mucosal architecture returned to normal in 4 patients at 4 weeks. The number of lamina propria mononuclear cells decreased because of a global reduction of CD4(+) and CD8(+) T lymphocytes and CD68(+) monocytes. Aberrant colonic epithelial HLA-DR expression completely disappeared. The percentage of intercellular adhesion molecule 1 and lymphocyte function-associated antigen 1-expressing and interleukin 4- and tumor necrosis factor-positive lamina propria mononuclear cells sharply decreased.
Infliximab dramatically decreases histological disease activity in Crohn's ileocolitis. Signs of active inflammation nearly disappear accompanied by a profound down-regulation of mucosal inflammatory mediators.
抗肿瘤坏死因子α单克隆抗体治疗(英夫利昔单抗)可减轻克罗恩病患者的临床体征和症状。本研究探讨了英夫利昔单抗对克罗恩病回结肠炎症黏膜组织病理学异常的影响。
13例激素抵抗型克罗恩病患者接受单次英夫利昔单抗输注(5 - 20mg/kg)治疗,5例接受安慰剂治疗。所有患者在治疗前及治疗后4周采集回肠和结肠活检标本。通过组织学评分评估炎症严重程度。采用抗HLA - DR、CD68、肿瘤坏死因子α、细胞间黏附分子1、淋巴细胞功能相关抗原、CD4、CD8和白细胞介素4抗体进行免疫组织化学染色。
英夫利昔单抗治疗后,回肠炎和结肠炎的组织学总活性评分均显著降低。这是由于中性粒细胞几乎消失和单核细胞减少所致。4周时4例患者的黏膜结构恢复正常。固有层单核细胞数量减少,原因是CD4(+)和CD8(+) T淋巴细胞及CD68(+)单核细胞整体减少。异常的结肠上皮HLA - DR表达完全消失。表达细胞间黏附分子1和淋巴细胞功能相关抗原1以及白细胞介素4和肿瘤坏死因子阳性的固有层单核细胞百分比急剧下降。
英夫利昔单抗可显著降低克罗恩病回结肠炎症的组织学疾病活性。活跃炎症迹象几乎消失,同时黏膜炎症介质显著下调。