Division of Pediatrics, Department of Reproductive and Developmental Medicine, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
J Clin Immunol. 2012 Feb;32(1):39-49. doi: 10.1007/s10875-011-9600-0. Epub 2011 Oct 13.
X-linked anhidrotic ectodermal dysplasia with immunodeficiency (X-EDA-ID) is caused by hypomorphic mutations in the gene encoding nuclear factor-κB essential modulator protein (NEMO). Patients are susceptibile to diverse pathogens due to insufficient cytokine and frequently show severe chronic colitis. An 11-year-old boy with X-EDA-ID was hospitalized with autoimmune symptoms and severe chronic colitis which had been refractory to immunosuppressive drugs. Since tumor necrosis factor (TNF) α is responsible for the pathogenesis of NEMO colitis according to intestinal NEMO and additional TNFR1 knockout mice studies, and high levels of TNFα-producing mononuclear cells were detected in the patient due to the unexpected gene reversion mosaicism of NEMO, an anti-TNFα monoclonal antibody was administered to ameliorate his abdominal symptoms. Repeated administrations improved his colonoscopic findings as well as his dry skin along with a reduction of TNFα-expressing T cells. These findings suggest TNF blockade therapy is of value for refractory NEMO colitis with gene reversion.
X 连锁无汗性外胚层发育不良伴免疫缺陷(X-EDA-ID)是由编码核因子-κB 必需调节剂蛋白(NEMO)的基因突变引起的。由于细胞因子不足,患者易感染多种病原体,并经常出现严重的慢性结肠炎。一名 11 岁男孩因自身免疫症状和严重的慢性结肠炎住院,该结肠炎对免疫抑制药物有抗药性。由于 TNF-α在肠道 NEMO 和其他 TNFR1 敲除小鼠研究中负责 NEMO 结肠炎的发病机制,并且由于 NEMO 的意外基因回复嵌合体,患者体内检测到高水平产生 TNFα的单核细胞,因此给予抗 TNFα单克隆抗体来改善他的腹部症状。重复给药改善了他的结肠镜检查结果,以及他的干燥皮肤,同时减少了 TNFα表达的 T 细胞。这些发现表明,TNF 阻断疗法对具有基因回复的难治性 NEMO 结肠炎具有价值。