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受体、抗体与疾病。

Receptors, antibodies, and disease.

作者信息

Blecher M

出版信息

Clin Chem. 1984 Jul;30(7):1137-56.

PMID:6329552
Abstract

Abnormal antibody production is now recognized as the basis of specific endocrine and neurological diseases and their complications. Among the autoimmune diseases, the best understood from a mechanistic point of view are myasthenia gravis, Graves' disease, several variants of insulin resistance, and a variant of bronchial asthma. In each of these human disorders, the clinical symptoms can be traced to the actions of antireceptor antibodies produced by a deranged immune system. The autoantibodies produced in these diseases are functionally heterogeneous. They may produce the clinical symptoms of hormone or neurotransmitter insufficiency either by blocking the binding of these agents to target cell surface receptors or by accelerating the internalization and degradation of these receptors. In other cases, the autoantibodies may produce the clinical signs of hormone excess by mimicking the actions of the hormone, in an uncontrollable fashion. In some cases, functionally different types of autoantibodies will appear in the same patient at different stages of the disease. For all of these autoantibodies, of whatever function, assays for their presence in serum are available, in forms suitable for clinical chemists, as well as for researchers; these will be described in this review. In addition to the known anti-receptor autoimmune diseases, there are a large number of other autoimmune diseases for which there is fragmentary evidence that their clinical symptoms have an anti-receptor autoantibody etiology. Several examples of this group will be discussed, and assays suitable for establishing the presence of anti-receptor antibodies in the sera of such patients will be provided. The disorders to be considered are: type I diabetes mellitus, chronic atrophic gastritis, autoimmune Addison's disease, autoimmune hypoparathyroidism, type II pseudohypoparathyroidism, resistant ovary syndrome, connective tissue diseases, and the HLA-B8/DR3 antigen haplotype as a potential marker for autoimmune diseases of the anti-receptor type.

摘要

异常抗体产生现已被确认为特定内分泌和神经疾病及其并发症的基础。在自身免疫性疾病中,从机制角度理解得最透彻的是重症肌无力、格雷夫斯病、几种胰岛素抵抗变体以及一种支气管哮喘变体。在这些人类疾病中,临床症状均可追溯到紊乱免疫系统产生的抗受体抗体的作用。这些疾病中产生的自身抗体在功能上具有异质性。它们可能通过阻断这些物质与靶细胞表面受体的结合,或加速这些受体的内化和降解,从而产生激素或神经递质不足的临床症状。在其他情况下,自身抗体可能通过以无法控制的方式模拟激素的作用,产生激素过量的临床体征。在某些情况下,功能不同类型的自身抗体可能会在疾病的不同阶段出现在同一患者体内。对于所有这些自身抗体,无论其功能如何,都有适用于临床化学家以及研究人员的血清检测方法;本文将对此进行描述。除了已知的抗受体自身免疫性疾病外,还有大量其他自身免疫性疾病,有零散证据表明其临床症状具有抗受体自身抗体病因。将讨论这一组疾病的几个例子,并提供适用于确定此类患者血清中抗受体抗体存在情况的检测方法。所考虑的疾病包括:I型糖尿病、慢性萎缩性胃炎、自身免疫性艾迪生病、自身免疫性甲状旁腺功能减退症、II型假性甲状旁腺功能减退症、抵抗卵巢综合征、结缔组织病,以及作为抗受体型自身免疫性疾病潜在标志物的HLA - B8/DR3抗原单倍型。

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