Pachlopnik Schmid Jana M, Junge Sonja A, Hossle Johann Peter, Schneider E Marion, Roosnek Eddy, Seger Reinhard A, Gungor Tayfun
Division of Immunology/Hematology/BMT, University Children's Hospital, Zurich, Switzerland.
Pediatrics. 2006 May;117(5):e1049-56. doi: 10.1542/peds.2005-2062. Epub 2006 Apr 24.
X-linked osteopetrosis, anhydrotic ectodermal dysplasia, and immunodeficiency (XL-O-EDA-ID) is a disorder that is caused by hypomorphic mutations in the nuclear factor kappaB essential modulator (NEMO). These mutations lead to an impaired NF-kappaB activation. In vitro analyses and studies in animal models show that inhibition of NF-kappaB leads to a decrease of cytokine production and T-cell proliferation. Patients classically display poor or delayed inflammatory response to infections. We describe a boy with XL-O-EDA-ID, 1167-1168insC NEMO mutation, and recurrent infections. In early infancy, he experienced hemophagocytosis with transient deficiency of natural killer activity. Increased immunoglobulin M levels in blood resulted from a monoclonal immunoglobulin M gammopathy. Blood T-cell numbers were constantly increased, most probably resulting from a peripheral T-cell expansion. Our observations suggest that patients with hypomorphic NEMO mutations and repeated infections may experience inflammatory dysregulation.
X连锁骨质石化症、无汗性外胚层发育不良和免疫缺陷综合征(XL-O-EDA-ID)是一种由核因子κB必需调节因子(NEMO)的亚效突变引起的疾病。这些突变导致NF-κB激活受损。体外分析和动物模型研究表明,NF-κB的抑制会导致细胞因子产生减少和T细胞增殖受抑。经典的患者对感染表现出炎症反应不良或延迟。我们描述了一名患有XL-O-EDA-ID、携带1167-1168insC NEMO突变且反复感染的男孩。在婴儿早期,他经历了噬血细胞增多症并伴有自然杀伤活性的短暂缺乏。血液中免疫球蛋白M水平升高是由单克隆免疫球蛋白M丙种球蛋白病引起的。血液中T细胞数量持续增加,很可能是外周T细胞扩增所致。我们的观察结果表明,患有NEMO亚效突变且反复感染的患者可能会出现炎症调节异常。