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首页> 外文期刊>Frontiers in Pediatrics >Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome
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Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome

机译:NFKB2中的新型杂合突变与早期发作CVID和NK细胞中的功能缺陷,通过弥散的CMV感染和严重的肾病综合征复杂化

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Nuclear factor kappa-B subunit 2 (NF-κB2/p100/p52), encoded by NFKB2 (MIM: 164012) belongs to the NF-κB family of transcription factors that play a critical role in inflammation, immunity, cell proliferation, differentiation and survival. Heterozygous C-terminal mutations in NFκB2 have been associated with early-onset common variable immunodeficiency (CVID), central adrenal insufficiency and ectodermal dysplasia. Only two previously reported cases have documented decreased natural killer (NK) cell cytotoxicity, and little is known about the role of NF-κB2 in NK cell maturation and function. Here we report a 13-year-old female that presented at 6 years of age with a history of early onset recurrent sinopulmonary infections, progressive hair loss, and hypogamaglobulinemia consistent with a clinical diagnosis of CVID. At 9 years of age she had cytomegalovirus (CMV) pneumonia that responded to ganciclovir treatment. Functional NK cell testing demonstrated decreased NK cell cytotoxicity despite normal NK cell numbers, consistent with a greater susceptibility to systemic CMV infection. Research exome sequencing (ES) was performed and revealed a novel de novo heterozygous nonsense mutation in NFKB2 (c.2611CT, p.Gln871*) that was not carried by either of her parents, the variant was Sanger sequenced and confirmed to be de novo in the patient. At age 12, she presented with a reactivation of the systemic CMV infection that was associated with severe and progressive nephrotic syndrome with histologic evidence of pedicellar effacement and negative immunofluorescence. To our knowledge, this is the third NF-κB2 deficient patient in which an abnormal NK cell function has been observed, suggesting a role for non-canonical NF-κB2 signaling in NK cell cytotoxicity. NK cell function should be assessed in patients with mutations in the non-canonical NF-κB pathway to explore the risk for systemic viral infections that may lead to severe complications and impact patient survival. Similarly NF-κB2 should be considered in patients with combined immunodeficiency who have aberrant NK cell function. Further studies are needed to characterize the role of NF-κB2 in NK cell cytotoxic function.
机译:由NFKB2(MIM:164012)编码的核因子Kappa-B亚基2(NF-κB2/ p100 / p52)属于NF-κB的转录因子系列,其在炎症,免疫,细胞增殖,分化和分化中发挥着关键作用生存。 NFκB2中的杂合性C末端突变与早发常见可变免疫缺陷(CVID),中央肾上腺功能不全和异常发育不良相关有关。只有两个先前报道的病例记录了天然杀伤(NK)细胞毒性下降,并且关于NK细胞成熟和功能中NF-κB2的作用很少。在这里,我们举报了一名13岁的女性,在6岁时呈现出早期发病的历史,其发作复发性中断,渐进式脱发和低阿巴比肝癌血症与CVID的临床诊断一致。在9岁时,她患有患有Ganciclovir治疗的胞嘧啶(CMV)肺炎。尽管正常的NK细胞数,功能性NK细胞测试证明了NK细胞细胞毒性降低,这与对系统性CMV感染的更大易感性一致。进行了研究exome测序(ES),并揭示了NFKB2(C.2611C​​> T,P.GLN871 *)中的新型Novo杂合子突变,这些父母未携带,该变异是Sanger测序并证实是De Novo在患者身上。在12岁时,她提出了与严重和渐进性肾病综合征有关的全身CMV感染的重新激活,所述肾病综合征与细胞学患病和负免疫荧光的组织学证据有关。据我们所知,这是已经观察到异常NK细胞功能的第三个NF-κB2缺陷患者,这表明在NK细胞细胞毒性中的非规范NF-κB2信号传导的作用。 NK细胞功能应在非规范NF-κB途径中的突变患者中进行评估,以探索可能导致严重并发症和影响患者存活的全身病毒感染的风险。类似地,应在具有异常NK细胞功能的患者中考虑NF-κB2。需要进一步的研究来表征NF-κB2在NK细胞毒性功能中的作用。

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