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共济失调毛细血管扩张症中的免疫缺陷

immunodeficiency in ataxia-telangiectasia.

作者信息

Biggar W D, Good R A

出版信息

Birth Defects Orig Artic Ser. 1975;11(1):271-6.

PMID:1096983
Abstract

Ataxia-telangiectasia is characterized by endocrine, neurologic, hematologic, hepatic, cutaneous and immunologic abnormalities. The immunologic deficiencies vary considerably from patient to patient, and in each patient with respect to time. The most frequent deficiencies of humoral immunity are diminished or absent serum and salivary IgA, diminished or absent serum IgE and impaired antibody responses to a variety of bacterial and viral antigens. Deficiencies of cellular immunity are commonly found by both in vivo and in vitro analyses. Histologic confirmation of these immunodeficiencies is readily observed in the lymphoid tissue. The thymus, which may be the seat of the primary abnormality in the immunodeficiency syndrome, regularly shows morphologic characteristics of an embryonic thymus.

摘要

共济失调毛细血管扩张症的特征为内分泌、神经、血液、肝脏、皮肤和免疫异常。免疫缺陷在患者之间差异很大,且在每个患者身上随时间变化。体液免疫最常见的缺陷是血清和唾液IgA减少或缺乏、血清IgE减少或缺乏以及对多种细菌和病毒抗原的抗体反应受损。细胞免疫缺陷通常通过体内和体外分析发现。在淋巴组织中很容易观察到这些免疫缺陷的组织学证实。胸腺可能是免疫缺陷综合征原发性异常的所在部位,通常显示出胚胎胸腺的形态特征。

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