Ia抗原和类风湿关节炎易感性。

Clinics in rheumatic diseases Pub Date : 1985-12-01
S H Lee, T Matsuyama, P Logalbo, J Silver, R J Winchester
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引用次数: 0

摘要

自从第一次描述人类白细胞凝集抗体以来,对MHC,特别是Ia区域的了解已经大大增加,现在它被认为是一个主要的多态多基因家族,参与免疫反应和疾病易感性的调节。这篇综述检验了在Ia系统中存在另一个复杂水平的假设,除了多个基因座和等位基因序列,它涉及到作为Ia分子功能重要组成部分的特定表位。这些表位中的某些可能负责调节免疫反应和对某些自身免疫性疾病(如类风湿关节炎)的易感性。有证据表明,某些单克隆抗体识别的表位与RA易感性的相关性明显高于现有的标记物,如DR4。对携带该表位的Ia分子的生化表征表明,相同的表位存在于两个不同的分子上。考虑到这种可能性,这些表位与主要参与产生RA患者特征的异常免疫状态的Ia决定因子密切相关,但不完全相同。
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Ia antigens and susceptibility to rheumatoid arthritis.

Since the first description of human leukocyte agglutination antibodies, knowledge of the MHC, particularly the Ia region, has grown immensely and it is now recognized as a major polymorphic multigene family involved in the regulation of immune response and disease susceptibility. This review examined the hypothesis that there is another level of complexity within the Ia system, beyond multiple loci and allelic series, that involves specific epitopes as the functionally important components of the Ia molecule. Certain of these epitopes are likely to be responsible for the regulation of immune responses and susceptibility to certain autoimmune diseases such as rheumatoid arthritis (RA). Evidence was presented that certain monoclonal antibodies recognize epitopes found in a significantly more positive association with susceptibility to RA than available markers such as DR4. Biochemical characterization of the Ia molecules bearing this epitope revealed that the same epitope was present on two different molecules. The possibility was considered that such epitopes are closely related but not identical to Ia determinants that are primarily involved in producing the abnormal immune state characterizing those with RA.

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