Yamauchi T, Naoe T, Kurosawa Y, Shiku H, Yamada K
Department of Internal Medicine, Nagoya University Branch Hospital, Japan.
Immunology. 1990 Jan;69(1):117-20.
This report describes the identification of autoantibodies that react with c-myc proteins in the sera of some patients with autoimmune diseases. Sera from nine to 30 patients, including six with systemic lupus erythematosus, one with mixed connective tissue disease, one with dermatomyositis and one with autoimmune haemolytic anaemia, reacted in immunoblotting assays against a truncated human c-myc protein p42 produced by Escherichia coli. Furthermore, these sera exhibited double bands of 58,000 and 60,000 MW in the nuclear fraction of HL-60 cells with the amplified c-myc gene. These bands were the same as those detected by the anti-human c-myc protein monoclonal antibody (MYC-1) by immunoblotting assay. The binding activities to 58,000 and 60,000 MW were not reduced by DNase I digestion with the sera and could be absorbed by a p42-bound affinity column and recovered after elution.
本报告描述了在一些自身免疫性疾病患者血清中鉴定出与c-myc蛋白发生反应的自身抗体。9至30名患者的血清,包括6名系统性红斑狼疮患者、1名混合性结缔组织病患者、1名皮肌炎患者和1名自身免疫性溶血性贫血患者,在免疫印迹试验中与大肠杆菌产生的截短型人c-myc蛋白p42发生反应。此外,这些血清在具有扩增c-myc基因的HL-60细胞核部分中呈现出58000和60000 MW的双条带。这些条带与通过免疫印迹试验用抗人c-myc蛋白单克隆抗体(MYC-1)检测到的条带相同。血清经DNase I消化后,与58000和60000 MW的结合活性并未降低,且可被p42结合亲和柱吸附,并在洗脱后回收。