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首页> 外文期刊>Frontiers in Immunology >Prospective Study of a Cohort of Russian Nijmegen Breakage Syndrome Patients Demonstrating Predictive Value of Low Kappa-Deleting Recombination Excision Circle (KREC) Numbers and Beneficial Effect of Hematopoietic Stem Cell Transplantation (HSCT)
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Prospective Study of a Cohort of Russian Nijmegen Breakage Syndrome Patients Demonstrating Predictive Value of Low Kappa-Deleting Recombination Excision Circle (KREC) Numbers and Beneficial Effect of Hematopoietic Stem Cell Transplantation (HSCT)

机译:一组俄罗斯尼梅尔断裂综合征患者的前瞻性研究,这些患者显示出低κ-缺失重组切除环(KREC)值的预测价值和造血干细胞移植(HSCT)的有益作用

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Background Nijmegen breakage syndrome (NBS) is a combined primary immunodeficiency with DNA repair defect, microcephaly, and other phenotypical features. It predominantly occurs in Slavic populations that have a high frequency of carriers with the causative NBN gene c.657_661del5 mutation. Due to the rarity of the disease in the rest of the world, studies of NBS patients are few. Here, we report a prospective study of a cohort of Russian NBS patients. Methods 35 Russian NBS patients of ages 1–19?years, referred to our Center between years 2012 and 2016, were prospectively studied. Results Despite the fact that in 80% of the patients microcephaly was diagnosed at birth or shortly thereafter, the average delay of NBS diagnosis was 6.5?years. Though 80% of the patients had laboratory signs of immunodeficiency, only 51% of the patients experienced significant infections. Autoimmune complications including interstitial lymphocytic lung disease and skin granulomas were noted in 34%, malignancies—in 57% of the patients. T-cell excision circle (TREC)/kappa-deleting recombination excision circle (KREC) levels were low in the majority of patients studied. Lower KREC levels correlated with autoimmune and oncological complications. Fifteen patients underwent hematopoietic stem cell transplantation (HSCT), 10 of them were alive and well, with good graft function. Three patients in the HSCT group and five non-transplanted patients died; tumor progression being the main cause of death. The probability of the overall survival since NBS diagnosis was 0.76 in the HSCT group and 0.3 in the non-transplanted group. Conclusion Based on our findings of low TRECs in most NBS patients, independent of their age, TREC detection can be potentially useful for detection of NBS patients during neonatal screening. KREC concentration can be used as a prognostic marker of disease severity. HSCT is a viable treatment option in NBS and should be especially considered in patients with low KREC numbers early on, before development of life-threatening complications.
机译:背景奈梅亨断裂综合症(NBS)是具有DNA修复缺陷,小头畸形和其他表型特征的原发性免疫缺陷综合症。它主要发生在斯拉夫族人群中,这些斯拉夫族人群的携带者携带高频率的NBN基因c.657_661del5突变。由于该疾病在世界其他地区很少见,因此对NBS患者的研究很少。在这里,我们报告了对俄罗斯NBS患者队列的前瞻性研究。方法对2012年至2016年间转诊至我们中心的35例1-19岁的俄罗斯NBS患者进行前瞻性研究。结果尽管有80%的患者在出生时或此后不久被诊断出小头畸形,但平均NBS诊断延迟时间为6.5年。尽管80%的患者有免疫缺陷的实验室征兆,但只有51%的患者经历了严重感染。在34%的恶性肿瘤中,有57%的患者注意到包括间质性淋巴细胞性肺病和皮肤肉芽肿在内的自身免疫并发症。在大多数研究的患者中,T细胞切除环(TREC)/κ缺失重组切除环(KREC)的水平较低。较低的KREC水平与自身免疫和肿瘤并发症相关。 15例患者接受了造血干细胞移植(HSCT),其中10例存活良好,移植功能良好。 HSCT组有3例患者和5例未移植的患者死亡。肿瘤进展是死亡的主要原因。自NBS诊断以来,总体存活率在HSCT组为0.76,在非移植组为0.3。结论基于我们对大多数NBS患者低TREC的发现,与他们的年龄无关,TREC检测对于新生儿筛查期间NBS患者的检测可能具有潜在的帮助。 KREC浓度可以用作疾病严重程度的预后指标。 HSCT在NBS中是一种可行的治疗选择,尤其是对于KREC值低的患者,应在威胁生命的并发症发生之前及早考虑。

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