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自身免疫性疾病的起始:重症肌无力早期进展过程中的独特型网络

The start of an autoimmune disease: idiotypic network during early progression of myasthenia gravis.

作者信息

Lefvert A K

机构信息

Department of Medicine, Karolinska Hospital, Stockholm.

出版信息

Ann Inst Pasteur Immunol. 1988 Nov-Dec;139(6):633-43. doi: 10.1016/0769-2625(88)90052-9.

Abstract

Anti-acetylcholine-receptor antibodies of IgG and IgM classes and antiidiotypic antibodies were determined in patients with myasthenia gravis at various times after the start of the disease. Patients with a disease duration of less than one year had a higher prevalence of antiidiotypic antibodies (31/32) than patients who had had the disease for more than 5 years (49/79), and the concentration of antiidiotypic antibodies was also higher in patients with early disease (p less than 0.005). The concentrations of antiidiotypic antibodies decreased during progression of the disease concomittant with an increase in IgG anti-receptor antibodies. A change from IgM to IgG anti-receptor antibody production was also found. In two patients, who developed myasthenia after bone-marrow grafting and who were followed before start of disease, antiidiotypic antibodies appeared before anti-receptor antibodies and before symptoms of myasthenia were present. The high prevalence and concentration of antiidiotypic antibodies in early disease indicate that development and expression of antiidiotypic antibodies are important in early myasthenia gravis.

摘要

在重症肌无力患者发病后的不同时间,检测了IgG和IgM类抗乙酰胆碱受体抗体及抗独特型抗体。病程小于1年的患者抗独特型抗体的患病率(31/32)高于病程超过5年的患者(49/79),且疾病早期患者抗独特型抗体的浓度也更高(p<0.005)。在疾病进展过程中,抗独特型抗体浓度下降,同时IgG抗受体抗体增加。还发现了抗受体抗体产生从IgM向IgG的转变。在两名骨髓移植后发生重症肌无力且在疾病开始前接受随访的患者中,抗独特型抗体在抗受体抗体之前以及重症肌无力症状出现之前就已出现。疾病早期抗独特型抗体的高患病率和浓度表明,抗独特型抗体的产生和表达在重症肌无力早期很重要。

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