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Heterogeneity of humoral immune abnormalities in children with Nijmegen breakage syndrome: an 8-year follow-up study in a single centre

机译:奈梅亨断裂综合征患儿体液免疫异常的异质性:在单个中心进行的为期8年的随访研究

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摘要

During an 8-year period of observation, defects of immune responses were characterized and monitored in 40 of 50 Polish children with Nijmegen breakage syndrome referred to the Children's Memorial Health Institute in Warsaw. The following parameters were determined at diagnosis: (1) concentrations of serum IgM, IgG, IgA; (2) concentrations of IgG subclasses; and (3) lymphocyte subpopulations. In addition, naturally acquired specific antibodies against Streptococcus pneumoniae were determined in 20 patients with a history of recurrent respiratory infections. During follow-up, total serum immunoglobulins and IgG subclasses were monitored systematically in 17 patients who did not receive immunomodulatory therapy. Moreover, anti-HBs antibody response was measured after vaccination of 20 children against HBV. We found that the immune deficiency in NBS is profound, highly variable, with a tendency to progress over time. Systematic monitoring of the humoral response, despite good clinical condition, is essential for early medical intervention.
机译:在为期8年的观察中,对50名患有奈梅亨断裂综合征的波兰儿童中的40名儿童进行了免疫反应缺陷的表征和监测,这些儿童被提交给华沙儿童纪念健康研究所。在诊断时确定以下参数:(1)血清IgM,IgG,IgA的浓度; (2)IgG亚类的浓度; (3)淋巴细胞亚群。另外,在20例有反复呼吸道感染史的患者中,确定了天然获得的抗肺炎链球菌特异性抗体。在随访期间,系统地监测了17例未接受免疫调节治疗的患者的血清总免疫球蛋白和IgG亚类。此外,在对20名儿童进行HBV疫苗接种后测量了抗HBs​​抗体反应。我们发现,国家统计局的免疫缺陷是深刻的,高度可变的,并且随着时间的推移会发展。尽管临床状况良好,但对体液反应的系统监测对于早期医学干预至关重要。

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