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白塞病组织受累的免疫遗传学基础。

An immunogenetic basis for the tissue involvement in Behçet's syndrome.

作者信息

Lehner T, Batchelor J R, Challacombe S J, Kennedy L

出版信息

Immunology. 1979 Aug;37(4):895-900.

Abstract

The multifocal involvement in Behçet's syndrome was grouped into a spectrum of four types, three of which appeared to have an immunogenetic basis. HLA-B5 was related to the ocular type of Behçet's syndrome (relative risk 7.3), HLA-B27 to the arthritic type (relative risk 12.1) and HLA-B12 to the muco-cutaneous type (relative risk 3.9). The concept that recurrent oral ulceration and Behçet's syndrome may belong to a disease spectrum is substantiated by the natural course of the disease. Furthermore, patients with recurrent oral ulcers share with the muco-cutaneous type of Behçet's syndrome a significantly increased frequency of HLA-B12 (relative risk 2.6). The HLA markers may also prove to be significant in the differential diagnosis and prognosis of a disease which may present under a confusing variety of clinical manifestations.

摘要

白塞病的多灶性病变分为四种类型,其中三种似乎具有免疫遗传学基础。HLA - B5与白塞病的眼型相关(相对风险7.3),HLA - B27与关节炎型相关(相对风险12.1),HLA - B12与黏膜皮肤型相关(相对风险3.9)。复发性口腔溃疡和白塞病可能属于同一疾病谱这一概念,已被该疾病的自然病程所证实。此外,复发性口腔溃疡患者与白塞病黏膜皮肤型患者一样,HLA - B12的频率显著增加(相对风险2.6)。HLA标志物在一种可能以各种令人困惑的临床表现出现的疾病的鉴别诊断和预后方面,可能也被证明具有重要意义。

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Behçet's syndrome and autoimmunity.白塞氏综合征与自身免疫
Br Med J. 1967 Feb 25;1(5538):465-7. doi: 10.1136/bmj.1.5538.465.
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Behçet's syndrome with arthritis.伴有关节炎的白塞病
Ann Rheum Dis. 1969 Mar;28(2):95-103. doi: 10.1136/ard.28.2.95.
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Reiter's disease and HL-A 27.赖特综合征与HL-A 27。
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