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Allogeneic hematopoietic stem cell transplantation in two brothers with DNA ligase IV deficiency: a case report and review of the literature

机译:双相造血干细胞移植在两兄弟中的DNA连接酶IV缺乏:案例报告和文学审查

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DNA ligase IV deficiency is a rare autosomal recessive disorder caused by hypomorphic mutations in the DNA ligase IV (LIG4) gene. DNA ligase IV is an essential protein for the development of a healthy immune system as well as for the protection of genomic integrity. Apart from typical stigmata, patients with DNA ligase IV deficiency are characterized by progressive bone marrow failure and a predisposition to malignancy. To our knowledge this reported case is the first description of two brothers with ligase IV deficiency who are treated with different hematopoietic stem cell transplantation (HSCT) regimens resulting in vastly divergent outcomes. The cases of two brothers suffering from severe recurrent infections and growth retardation are described. The laboratory findings showed pancytopenia with significant lymphopenia. The two boys were diagnosed with DNA ligase IV deficiency, associated with severe combined immunodeficiency (SCID). Both patients received HSCT from two different matched unrelated donors (MUD) at the age of 33 and 18?months. The older brother succumbed post-transplant due to fatal side-effects 143?days after allogeneic HSCT. The younger brother – conditioned with a different regimen – received a T cell depleted graft 4 months later. No severe side-effects occurred, neither post-transplant nor in the following years. Ten years after HSCT the patient is well off, living a normal life and attending a regular high school. His immune system is fully reconstituted, resulting in a maximum of T cell receptor (TCR) diversity, which is a prerequisite for immune competence. However, he still suffers from microcephaly, dwarfism and dystrophy. This case report gives an example of a successful HSCT as a treatment option in a genetic disorder such as ligase IV deficiency, using a rather mild conditioning regimen. Further studies are required to determine the viability and efficacy of this treatment option.
机译:DNA连接酶IV缺乏是DNA连接酶IV(Lig4)基因中的低晶体突变引起的稀有常染色体隐性疾病。 DNA连接酶IV是一种基本蛋白质,用于开发健康的免疫系统以及保护基因组完整性。除了典型的柱状,DNA连接酶IV缺陷的患者的特征在于进行骨髓骨髓衰竭和恶性肿瘤的易感性。据我们所知,这一报告的案例是两种兄弟的第一次描述,其中两种患有不同的造血干细胞移植(HSCT)方案治疗,导致巨大发散的结果。描述了两种患有严重的复发感染和生长迟缓的兄弟的病例。实验室发现显示了具有重要淋巴细胞增长的植物特迟。这两个男孩被诊断​​出患有DNA连接酶IV缺乏症,与严重的免疫缺陷(SCID)相关。两名患者在33岁和18岁时接受了两个不同匹配的无关捐助者(泥浆)的HSCT。由于致命的副作用143?同种异体的HSCT后天数,哥哥屈服于移植后。弟弟 - 有不同的方案,4个月后接受了T细胞耗尽的移植物。没有发生严重的副作用,既没有移植后也不是在接下来的几年内。在HSCT患者休息时十年,生活正常生活并参加正常的高中。他的免疫系统完全重构,导致T细胞受体(TCR)多样性,这是免疫能力的先决条件。然而,他仍然患有微微术,侏儒症和营养不良症。本病例报告给出了遗传障碍等治疗选择的成功HSCT,例如连接酶IV缺乏,使用相当温和的调理方案。需要进一步的研究来确定该处理选项的活力和功效。

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