Department of Pediatric Pneumonology, Immunology and Intensive Care Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Laboratory of Lymphocyte Activation and Susceptibility to EBV infection, Institut National de la Santé et de la Recherche Médicale UMR 1163, Paris, France.
Front Immunol. 2020 Aug 4;11:1593. doi: 10.3389/fimmu.2020.01593. eCollection 2020.
Most of the few patients with homozygous CD70 deficiency described to date suffered from EBV-related malignancies in early childhood. We present a woman with CD70 deficiency diagnosed in adulthood. She presented in childhood with recurrent airway infections due to encapsulated bacteria, herpes zoster and a fulminant EBV infection followed by chronic EBV infection with mild lymphoproliferation and severe gingivitis/periodontal disease with high EBV viral load in saliva and gingival plaques as an adult. Up to the age of 24 years she developed no malignancy despite constant EBV viremia since primary EBV infection 15 years previously. Immunologic evaluation in childhood showed hypogammaglobulinemia with impaired polysaccharide responsiveness. She has been stable on immunoglobulin substitution with no further severe viral infections and no bacterial airway infections in adulthood. Targeted panel sequencing at the age of 20 years revealed a homozygous missense mutation (ENST00000245903.3:c.2T>C). CD70 deficiency was confirmed by absent CD70 expression of B cells and activated T cell blasts. The patient finished high school, persues an academic career and has rarely sick days at college. The clinical course of our patient may help to counsel parents of CD70-deficient patients with regard to prognosis and therapeutic options including haematopoetic stem cell transplantation.
迄今为止,大多数描述的纯合 CD70 缺乏症患者在幼年时患有 EBV 相关恶性肿瘤。我们介绍一位成年期诊断为 CD70 缺乏症的女性患者。她在儿童时期因包膜细菌、带状疱疹和暴发性 EBV 感染而反复出现呼吸道感染,随后出现慢性 EBV 感染,伴有轻度淋巴增生和严重的牙龈炎/牙周病,唾液和牙龈斑块中的 EBV 病毒载量很高。尽管自 15 年前原发性 EBV 感染以来一直存在 EBV 病毒血症,但直到 24 岁,她仍未发生恶性肿瘤。儿童时期的免疫评估显示免疫球蛋白低下,多糖反应受损。她一直在接受免疫球蛋白替代治疗,成年后没有再发生严重的病毒感染或细菌性呼吸道感染。20 岁时进行的靶向panel 测序显示存在纯合错义突变(ENST00000245903.3:c.2T>C)。B 细胞和激活的 T 细胞母细胞中缺乏 CD70 表达,从而证实存在 CD70 缺乏症。该患者完成了高中学业,从事学术职业,在大学期间很少请病假。我们患者的临床病程可能有助于向 CD70 缺乏症患者的父母提供预后和治疗选择方面的咨询,包括造血干细胞移植。