Salt Bryn H, Niemela Julie E, Pandey Rahul, Hanson Eric P, Deering Raquel P, Quinones Ralph, Jain Ashish, Orange Jordan S, Gelfand Erwin W
Department of Pediatrics, National Jewish Medical and Research Center, Denver, CO 80206, USA.
J Allergy Clin Immunol. 2008 Apr;121(4):976-82. doi: 10.1016/j.jaci.2007.11.014. Epub 2008 Jan 7.
Patients with hypomorphic nuclear factor-kappaB essential modulator (NEMO) mutations have extensive phenotypic variability that can include atypical infectious susceptibility.
This study may provide important insight into immunologic mechanisms of host defense.
Immunologic evaluation, including studies of Toll-like receptor (TLR) function, was performed in a 6-month-old boy with normal ectodermal development who was diagnosed with Pneumocystis pneumonia and cytomegalovirus sepsis.
Genomic and cDNA sequencing demonstrated a novel NEMO missense mutation, 337G->A, predicted to cause a D113N (aspartic acid to asparagine) substitution in the first coiled-coil region of the NEMO protein. Quantitative serum immunoglobulins, lymphocyte subset numbers, and mitogen-induced lymphocyte proliferation were essentially normal. The PBMC responses to TLR ligands were also surprisingly normal, whereas natural killer cell cytolytic activity, T-cell proliferative responses to specific antigens, and T-cell receptor-induced NF-kappaB activation were diminished.
Unlike the unique NEMO mutation described here, the most commonly reported mutations are clustered at the 3' end in the tenth exon, which encodes a zinc finger domain. Because specific hypomorphic variants of NEMO are associated with distinctive phenotypes, this particular NEMO mutation highlights a dispensability of the region including amino acid 113 for TLR signaling and ectodysplasin A receptor function. This region is required for certain immunoreceptor functions as demonstrated by his susceptibility to infections as well as natural killer cell and T-cell defects.
低功能核因子-κB必需调节因子(NEMO)突变患者具有广泛的表型变异性,可包括非典型感染易感性。
本研究可能为宿主防御的免疫机制提供重要见解。
对一名6个月大、外胚层发育正常、被诊断为肺孢子菌肺炎和巨细胞病毒败血症的男孩进行了免疫评估,包括Toll样受体(TLR)功能研究。
基因组和cDNA测序显示了一种新的NEMO错义突变,337G→A,预计会在NEMO蛋白的第一个卷曲螺旋区域导致D113N(天冬氨酸变为天冬酰胺)替代。血清定量免疫球蛋白、淋巴细胞亚群数量和丝裂原诱导的淋巴细胞增殖基本正常。PBMC对TLR配体的反应也出人意料地正常,而自然杀伤细胞的溶细胞活性、T细胞对特定抗原的增殖反应以及T细胞受体诱导的NF-κB激活则减弱。
与本文所述的独特NEMO突变不同,最常报道的突变集中在第十外显子的3'端,该外显子编码一个锌指结构域。由于NEMO的特定低功能变体与独特的表型相关,这种特定的NEMO突变突出了包括氨基酸113在内的区域对于TLR信号传导和外胚层发育不良蛋白A受体功能的非必需性。正如他对感染的易感性以及自然杀伤细胞和T细胞缺陷所表明的,该区域对于某些免疫受体功能是必需的。