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儿童普通可变免疫缺陷中的淋巴细胞特征。

Lymphocyte characteristics in children with common variable immunodeficiency.

机构信息

Department of Pediatric Immunology and Infectious Diseases, Wilhelmina Children's Hospital, Utrecht, The Netherlands.

出版信息

Clin Immunol. 2010 Apr;135(1):63-71. doi: 10.1016/j.clim.2009.11.010. Epub 2009 Dec 16.

Abstract

The diagnosis of common variable immunodeficiency (CVID) is reserved for patients who suffer from undefined B cell dysfunction. Division of the CVID population into subgroups enables research for underlying disease causes. We studied clinical features and lymphocyte characteristics in 38 children with CVID and compared them to 30 children with less severe antibody deficiencies (e.g. specific antibody deficiency combined with IgG subclass deficiency) and with 65 pediatric controls. Most pediatric immune phenotypes were comparable to adult CVID phenotypes, including a selective increase in newly formed B cells and a decrease in memory B cells and CD4(+) T cells. Eighteen percent of pediatric patients had a mutation in the TNFRSF13B gene, which requires further investigation. Finally, pediatric patients with decreased class-switched memory B cells had significantly more complications. A pediatric classification for CVID may enable prediction and early diagnosis of disease related complications and provide a framework for further etiologic research.

摘要

普通可变免疫缺陷症(CVID)的诊断仅限于患有未明确的 B 细胞功能障碍的患者。将 CVID 人群分为亚组,可用于研究潜在的疾病原因。我们研究了 38 名 CVID 儿童的临床特征和淋巴细胞特征,并将其与 30 名抗体缺乏症较轻的儿童(例如特异性抗体缺乏症合并 IgG 亚类缺乏症)和 65 名儿科对照进行了比较。大多数儿科免疫表型与成人 CVID 表型相似,包括新形成的 B 细胞选择性增加,记忆 B 细胞和 CD4(+)T 细胞减少。18%的儿科患者存在 TNFRSF13B 基因突变,需要进一步研究。最后,类转换记忆 B 细胞减少的儿科患者并发症明显更多。CVID 的儿科分类可能能够预测和早期诊断与疾病相关的并发症,并为进一步的病因学研究提供框架。

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