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类风湿关节炎的标志物抗体:诊断及发病机制意义

Marker antibodies of rheumatoid arthritis: diagnostic and pathogenetic implications.

作者信息

Aho K, Palusuo T, Kurki P

机构信息

National Public Health Institute, Helsinki, Finland.

出版信息

Semin Arthritis Rheum. 1994 Jun;23(6):379-87. doi: 10.1016/0049-0172(94)90088-4.

Abstract

Rheumatoid arthritis (RA) is associated with several autoantibodies specific enough to serve as diagnostic and prognostic markers. These include rheumatoid factor (RF), antikeratin antibody (AKA), antiperinuclear factor (APF), and anti-RA33. The first three, and possibly also anti-RA33, may precede the onset of clinical RA. The prevalence of positive test reactions depends on the period between taking the specimen and onset of disease; when the period is short, the prevalence is nearly the same as in established disease. Thus, RA has a long asymptomatic period with broadening immunological activity. The assays for AKA and APF (and possibly also for anti-RA33), compared with RF testing, yielded greater specificity rather than the ability to define any subgroup with particularly severe disease. Used together, the above marker antibodies may form a new and more enlightened basis for defining seropositive RA. It is commonly believed that genetically mediated immune response plays an important role in the initiation of RA. However, the role of the major histocompatibility complex antigens may be in modulation of the inflammatory reaction in a later phase.

摘要

类风湿关节炎(RA)与几种特异性足以作为诊断和预后标志物的自身抗体相关。这些抗体包括类风湿因子(RF)、抗角蛋白抗体(AKA)、抗核周因子(APF)和抗RA33。前三种抗体,可能还有抗RA33,可能在临床RA发病之前就已出现。检测反应阳性的患病率取决于采集标本与疾病发作之间的时间间隔;当时间间隔较短时,患病率与确诊疾病时几乎相同。因此,RA有很长的无症状期,且免疫活性不断增强。与RF检测相比,AKA和APF(可能还有抗RA33)检测具有更高的特异性,而非用于定义任何疾病特别严重的亚组的能力。上述标志物抗体联合使用,可能为定义血清阳性RA形成一个新的、更具启发性依据。人们普遍认为,基因介导的免疫反应在RA的发病中起重要作用。然而,主要组织相容性复合体抗原的作用可能在后期炎症反应的调节中发挥作用。

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