原发性免疫缺陷的eb病毒感染和肿瘤发生。

AIDS research Pub Date : 1986-12-01
M Okano, T Osato, S Koizumi, S Imai, T Aya, S Fujiwara, F Mizuno, Y Sakiyama, S Matsumoto, O Sugawara
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引用次数: 0

摘要

16例日本共济失调毛细血管扩张症(AT)和Wiskott-Aldrich综合征(WAS)患者中有3例发生淋巴瘤。患者有持续再激活的eb病毒(EBV)感染,病毒特异性细胞免疫力显著下降。在这些患者中,B淋巴细胞对ebv诱导的事件和细胞原癌基因激活比健康人更敏感。这种免疫和遗传背景被认为可以解释这些原发性免疫缺陷疾病的大量淋巴细胞增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epstein-Barr virus infection and oncogenesis in primary immunodeficiency.

Lymphomas occurred in 3 of 16 Japanese patients with ataxia telangiectasia (AT) and Wiskott-Aldrich syndrome (WAS). The patients had a persistently reactivated Epstein-Barr virus (EBV) infection with a remarkable decrease in virus-specific cellular immunity. In these patients, the B lymphocytes were more sensitive to EBV-induced events and to cellular proto-oncogene activation than seen in the healthy counterparts. This immunologic and genetic background was considered to explain the massive lymphoproliferation in these primary immunodeficiency disorders.

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