全外显子组测序用于吞噬细胞性淋巴组织增生症突变筛选

E. S. Rahmani, M. Fathi, M. Abazari, Hojat Shahraki, Vahid Ziaee Fellow, H. Rahimi, Arshad Hosseini
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引用次数: 0

摘要

背景:噬血细胞性淋巴组织细胞增多症(HLH)是一种免疫系统疾病,其特征是由活化但无效的细胞毒性细胞引起的高细胞素血症引起的不受控制的高炎症。由于这种疾病与恶性淋巴瘤和白血病等其他疾病的相似性以及两种形式的相似性,对HLH患者进行正确的诊断是困难的,而且并不总是成功的。此外,由于基因座和等位基因的异质性,HLH的分子特征是一个具有挑战性的问题。材料和方法:在本实验研究中,采用全外显子组测序(WES)对一个伊朗四口家庭进行突变检测,该家庭的儿童患有HLH病的体征和症状。在Linux操作系统上使用多步骤的内部WES方法进行数据分析。结果:本研究在UNC13D基因第6外显子中检测到一个纯合核苷酸替代突变(c.551G> a:p.W184*)。W184*驱动到一个过早终止密码子,因此产生一个截断的蛋白。这种突变从父母遗传给一个4个月大的女婴,具有常染色体隐性模式。亲本携带W184*杂合型,无任何症状。患者临床表现为发热、腹泻、肝脾肿大、高铁蛋白水平,有HLH家族史。W184*对细胞毒性T淋巴细胞和自然杀伤细胞具有破坏作用。这两种没有UNC13D基因健康产物的免疫系统细胞将无法将有毒颗粒排入突触空间,因此免疫反应中的炎症并没有消失。结论:根据本研究,WES是一种可靠、快速、经济的HLH患者分子特征分析方法。此外,本研究引入的WES专用数据分析平台可能提供高速分析步骤。这个免费的平台不需要在线提交数据。
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Whole Exome Sequencing for Mutation Screening in Hemophagocytic Lymphohistiocytosis
Background: Hemophagocytic lymphohistiocytosis (HLH) is an immune system disorder characterized by uncontrolled hyper-inflammation owing to hypercytokinemia from the activated but ineffective cytotoxic cells. Establishing a correct diagnosis for HLH patients due to the similarity of this disease with other conditions like malignant lymphoma and leukemia and similarity among its two forms is difficult and not always a successful procedure. Besides, the molecular characterization of HLH due to the locus and allelic heterogeneity is a challenging issue. Materials and Methods: In this experimental study, whole exome sequencing (WES) was used for mutation detection in a four-member Iranian family with children suffering from signs and symptoms of HLH disease. Data analysis was performed by using a multi-step in-house WES approach on Linux OS. Result: In this study, a homozygous nucleotide substitution mutation (c.551G>A:p.W184*) was detected in exon number six of the UNC13D gene. W184* drives to a premature stop codon, so produce a truncated protein. This mutation inherited from parents to a four-month female infant with an autosomal recessive pattern. Parents were carrying out the heterozygous form of W184* without any symptoms. The patient showed clinical signs such as fever, diarrhea, hepatosplenomegaly, high level of ferritin, and a positive family history of HLH disease. W184* has a damaging effect on cytotoxic T lymphocytes, and natural killer cells. These two types of immune system cells without a healthy product of the UNC13D gene will be unable to discharge toxic granules into the synaptic space, so the inflammation in the immune response does not disappear. Conclusion: According to this study, WES can be a reliable, fast, and cost-effective approach for the molecular characterization of HLH patients. Plus, WES specific data analysis platform introduced by this study potentially offers a high-speed analysis step. This cost-free platform doesn't require online data submission.
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来源期刊
CiteScore
0.80
自引率
33.30%
发文量
33
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