Lando P, Gabriel J, Berzins K, Perlmann P
Department of Immunology, University of Stockholm, Sweden.
Scand J Immunol. 1980;11(3):253-60. doi: 10.1111/j.1365-3083.1980.tb00233.x.
The immunoglobulin class of the complement-dependent cytotoxic antibodies in serum from D23 hepatoma-bearing rats (D23 TBS) for D23 hepatoma cells was analysed. When studied by affinity chromatography with concanavalin A, protamine, or staphylococcal protein A conjugated to Sepharose, the cytotoxic activity bound to the former two but not protein A. The binding fractions were further characterized by column chromatography on Sepharose CL-4B. The cytotoxic activity was recovered exclusively in the high molecular weight fractions corresponding to human IgM. Monitoring with IgG- or IgM-specific rabbit antibodies indicated that these high molecular weight cytotoxic fractions contained both IgG and IgM. However, fractionation of D23 TBS at low pH suggested that cytotoxicity was due to IgM antibodies rather than to immune-complexed IgG antibodies. This was supported by the findings that rabbit antirat IgM antibodies inhibited the cytotoxicity of TBS completely when added at high dilutions.
分析了荷D23肝癌大鼠血清(D23 TBS)中针对D23肝癌细胞的补体依赖性细胞毒性抗体的免疫球蛋白类别。当用与琼脂糖偶联的伴刀豆球蛋白A、鱼精蛋白或葡萄球菌蛋白A通过亲和层析进行研究时,细胞毒性活性与前两者结合,但不与蛋白A结合。结合部分通过在琼脂糖CL-4B上进行柱层析进一步表征。细胞毒性活性仅在对应于人IgM的高分子量部分中回收。用IgG或IgM特异性兔抗体监测表明,这些高分子量细胞毒性部分同时含有IgG和IgM。然而,在低pH下对D23 TBS进行分级分离表明,细胞毒性是由于IgM抗体而非免疫复合物IgG抗体。当以高稀释度添加时,兔抗大鼠IgM抗体完全抑制TBS的细胞毒性,这一发现支持了上述结论。