首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Epstein-Barr serology in immunodeficiencies: an attempt to correlate with immune abnormalities in Wiskott-Aldrich and Chediak-Higashi syndromes and ataxia telangiectasia.
【2h】

Epstein-Barr serology in immunodeficiencies: an attempt to correlate with immune abnormalities in Wiskott-Aldrich and Chediak-Higashi syndromes and ataxia telangiectasia.

机译:免疫缺陷的爱泼斯坦-巴尔血清学:试图与维斯科特-奥尔德里奇和切迪亚克-东综合症以及共济失调毛细血管扩张症的免疫异常相关联。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Epstein-Barr (EB) virus serology was correlated with the results of immunological investigations of three inherited immunodeficiency diseases, in an attempt to understand the immune mechanisms controlling EB virus infection. In nine patients with Wiskott-Aldrich syndrome (WAS), the constant lack of anti-EB virus associated nuclear antigen (EBNA) was accompanied by a consistent impairment of allogeneic cytotoxicity. We confirmed a frequent absence of anti-EBNA antibody in ataxia telangiectasia (AT), and we showed a correlation between the level of anti-EBNA response and the mixed leucocyte response (MLR), i.e., an absence of anti-EBNA antibody correlated with a decreased MLR. In two of three untreated patients with Chediak-Higashi syndrome (CHS), high persistent titres of anti-EA antibodies were observed, which were possibly related to a defective natural killer (NK) cell activity. In spite of previous infection with EB virus, none of the 41 patients exhibited clinical signs attributable to the virus, suggesting that residual or compensatory mechanisms must have limited activation of the virus. In patients with AT and WAS these mechanisms may include NK cell activity, which is not depressed in these syndromes, whereas in patients with CHS, they may involve T cell cytotoxicity.
机译:为了了解控制EB病毒感染的免疫机制,将爱泼斯坦-巴尔(EB)病毒血清学与三种遗传性免疫缺陷疾病的免疫学调查结果相关联。在9名Wiskott-Aldrich综合征(WAS)患者中,抗EB病毒相关核抗原(EBNA)的持续缺乏伴随着同种异体细胞毒性的持续损害。我们证实了共济失调性毛细血管扩张症(AT)中经常缺少抗EBNA抗体,并且我们显示了抗EBNA应答水平与混合白细胞应答(MLR)之间存在相关性,即不存在与EBNA相关的抗EBNA抗体。 MLR降低。在三名患有Chediak-Higashi综合征(CHS)的未经治疗的患者中,有两例观察到高持续滴度的抗EA抗体,这可能与自然杀伤(NK)细胞活性缺陷有关。尽管先前曾感染EB病毒,但41例患者均未显示可归因于该病毒的临床体征,这表明残留或补偿机制必须限制了该病毒的激活。在患有AT和WAS的患者中,这些机制可能包括NK细胞活性,而在这些综合征中并不降低这种活性,而在患有CHS的患者中,它们可能涉及T细胞的细胞毒性。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号