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X连锁淋巴增生综合征(XLP)男孩中的爱泼斯坦-巴尔病毒诱导疾病:登记研究的最新进展

Epstein-Barr virus-induced diseases in boys with the X-linked lymphoproliferative syndrome (XLP): update on studies of the registry.

作者信息

Purtilo D T, Sakamoto K, Barnabei V, Seeley J, Bechtold T, Rogers G, Yetz J, Harada S

出版信息

Am J Med. 1982 Jul;73(1):49-56. doi: 10.1016/0002-9343(82)90923-8.

Abstract

Analyses of 100 subjects with the X-linked lymphoproliferative syndrome (XLP) in 25 kindreds revealed four major interrelated phenotypes: infectious mononucleosis, malignant B-cell lymphoma, aplastic anemia, and hypogammaglobulinemia. Eighty-one of the patients died. Two male subjects were asymptomatic but showed immunodeficiency to Epstein-Barr virus (EBV). Seventy-five subjects had the infectious mononucleosis phenotype and concurrently, 17 subjects of this group had aplastic anemia. All subjects with aplastic anemia died within a week. Aplastic anemia did not accompany hypogammaglobulinemia or malignant lymphoma phenotypes. Hypogammaglobulinemia had been detected before infectious mononucleosis in three subjects, after infectious mononucleosis in five subjects, and was not associated with infectious mononucleosis in 11 boys with hypogammaglobulinemia. In nine subjects infectious mononucleosis appeared to have evolved into malignant lymphoma; however, the majority of patients with malignant lymphoma showed no obvious antecedent infectious mononucleosis. One subject had infectious mononucleosis following recurrent malignant lymphoma. Twenty-six of 35 lymphomas were in the terminal ileum. Results of immunologic and virologic studies of 15 survivors revealed combined variable immunodeficiency and deficient antibody responses to EBV-specific antigens. Mothers of boys with XLP exhibited abnormally elevated titers of antibodies of EBV. Subjects of both sexes with phenotypes of XLP should be investigated for immunodeficiency to EBV. Persons with inherited or acquired immunodeficiency may be vulnerable to life-threatening EBV-induced diseases.

摘要

对25个家族中100名患有X连锁淋巴增生综合征(XLP)的受试者进行分析后发现了四种主要的相互关联的表型:传染性单核细胞增多症、恶性B细胞淋巴瘤、再生障碍性贫血和低丙种球蛋白血症。81名患者死亡。两名男性受试者无症状,但对爱泼斯坦-巴尔病毒(EBV)表现出免疫缺陷。75名受试者具有传染性单核细胞增多症表型,同时,该组中有17名受试者患有再生障碍性贫血。所有再生障碍性贫血患者均在一周内死亡。再生障碍性贫血不伴有低丙种球蛋白血症或恶性淋巴瘤表型。在3名受试者中,低丙种球蛋白血症在传染性单核细胞增多症之前被检测到,在5名受试者中在传染性单核细胞增多症之后被检测到,在11名患有低丙种球蛋白血症的男孩中与传染性单核细胞增多症无关。在9名受试者中,传染性单核细胞增多症似乎已演变成恶性淋巴瘤;然而,大多数恶性淋巴瘤患者没有明显的前期传染性单核细胞增多症病史。一名受试者在复发性恶性淋巴瘤后出现传染性单核细胞增多症。35例淋巴瘤中有26例位于回肠末端。对15名幸存者进行的免疫学和病毒学研究结果显示,存在联合可变免疫缺陷以及对EBV特异性抗原的抗体反应不足。患有XLP的男孩的母亲表现出EBV抗体滴度异常升高。患有XLP表型的男女受试者均应接受针对EBV免疫缺陷的检查。患有遗传性或获得性免疫缺陷的人可能易患危及生命的EBV诱导疾病。

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