Infliximab regulates lamina propria T lymphocytes in patients with Crohn's disease

O. WATANABE, T. ANDO, R. FURUTA, O. MAEDA, K. ISHIGURO, H. TAKAHASHI, K. INA,  K. KUSUGAMI, H. GOTO
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Abstract

Summary

Background and Aims

The immune system is a major determinant of the pathophysiological inflammation, which may lead to gastrointestinal mucosal injury in patients with Crohn's disease. Cytokines such as tumour necrosis factor-alpha are well-known mediators of the immune system, and treatment with a chimeric anti-tumour necrosis factor-alpha antibody (infliximab) has been shown to be highly effective in patients with Crohn's disease. Recent evidence indicates that infliximab induces apoptosis in lamina propria T lymphocytes in these patients. To better understand the mechanisms of infliximab's effect on gastrointestinal inflammation, we investigated changes in the serum level of cytokines after treatment in these patients, and the effect of infliximab in inducing the apoptosis of T lymphocytes.

Methods

Thirteen patients with Crohn's disease were treated with infliximab at a dosage of 5-mg/kg body weight. Clinical response was evaluated using the Crohn's Disease Activity Index, and serum soluble interleukin-2 receptor, interleukin-6, tumour necrosis factor-alpha levels were analysed by enzyme-linked immunosorbent assay at 0 and 2 weeks after treatment. Apoptosis of peripheral and lamina propria T lymphocytes after culture with infliximab was detected by flow cytometry.

Results

Crohn's Disease Activity Index decreased in 12 of 13 patients, and serum soluble interleukin-2 receptor, interleukin-6 and tumour necrosis factor-alpha levels decreased in most patients after treatment with infliximab. Tumour necrosis factor-alpha level before treatment in the six patients in whom Crohn's Disease Activity Index decreased by more than 70 was <5 ng/mL. Infliximab induced the apoptosis of lamina propria but not of peripheral T lymphocytes.

Conclusion

These findings suggest that a low level of serum tumour necrosis factor-alpha is an indicator for infliximab treatment. The induction of apoptosis of lamina propria T lymphocytes by infliximab may be an important mechanism of its anti-inflammatory effect in patients with Crohn's disease.

英夫利昔单抗调节克罗恩病患者固有层T淋巴细胞
背景与目的免疫系统是病理生理性炎症的主要决定因素,可导致克罗恩病患者胃肠道黏膜损伤。细胞因子如肿瘤坏死因子- α是众所周知的免疫系统介质,嵌合抗肿瘤坏死因子- α抗体(英夫利昔单抗)治疗已被证明对克罗恩病患者非常有效。最近的证据表明,英夫利昔单抗可诱导这些患者固有层T淋巴细胞凋亡。为了更好地了解英夫利昔单抗治疗胃肠道炎症的作用机制,我们研究了这些患者治疗后血清细胞因子水平的变化,以及英夫利昔单抗诱导T淋巴细胞凋亡的作用。方法对13例克罗恩病患者采用英夫利昔单抗治疗,剂量为5mg /kg体重。采用克罗恩病活动性指数评估临床疗效,并在治疗后0周和2周采用酶联免疫吸附法分析血清可溶性白细胞介素-2受体、白细胞介素-6、肿瘤坏死因子- α水平。用流式细胞术检测英夫利昔单抗培养后外周血和固有层T淋巴细胞的凋亡情况。结果13例患者中12例患者克罗恩病活动性指数下降,大多数患者在英夫利昔单抗治疗后血清可溶性白细胞介素-2受体、白细胞介素-6和肿瘤坏死因子- α水平下降。6例克罗恩病活动性指数下降大于70的患者治疗前肿瘤坏死因子α水平为5 ng/mL。英夫利昔单抗诱导固有层细胞凋亡,但不诱导外周T淋巴细胞凋亡。结论血清肿瘤坏死因子- α水平低是英夫利昔单抗治疗的一个指标。英夫利昔单抗诱导克罗恩病患者固有层T淋巴细胞凋亡可能是其抗炎作用的重要机制。
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