van der Meulen F W, de Bruin H G, Goosen P C, Bruynes E C, Joustra-Maas C J, Telkamp H G, von dem Borne A E, Engelfriet C P
Br J Haematol. 1980 Sep;46(1):47-56. doi: 10.1111/j.1365-2141.1980.tb05934.x.
The purpose of this study was to determine whether quantitative or qualitative factors are of major importance in the destruction of red cells sensitized with incomplete warm autoantibodies of subclass IgG1. To that end, the relative amount of igG1 antibody present on the red cells of patients with autoantibodies of this subclass only, was measured by means of continuous flow cytofluorometry. This method appeared to give an idea of the amount of antibody on red cells and was reproducible. The intensity of the fluorescence of patient's red cells, measured after incubation with a FITC-labelled anti-IgG1, was compared with the presence or absence of signs of increased haemolysis in vivo and the cytotoxic activity of normal monocytes towards these red cells in vitro. It appearedthat it was predominantly the amount of IgG1 autoantibody that determined whether or not these antibodies induced haemolysis in vivo or cytotoxicity of monocytes in vitro. This was also true with methyldopa-induced IgG1 autoantibodies.
本研究的目的是确定在破坏由IgG1亚类不完全温自身抗体致敏的红细胞过程中,定量因素还是定性因素起主要作用。为此,通过连续流动细胞荧光测定法,测量了仅患有此类亚类自身抗体患者红细胞上存在的IgG1抗体的相对量。该方法似乎能给出红细胞上抗体量的概念,且具有可重复性。将患者红细胞与异硫氰酸荧光素标记的抗IgG1孵育后测得的荧光强度,与体内溶血增加迹象的有无以及正常单核细胞对这些红细胞的体外细胞毒性活性进行了比较。结果表明,主要是IgG1自身抗体的量决定了这些抗体是否在体内诱导溶血或在体外诱导单核细胞的细胞毒性。甲基多巴诱导的IgG1自身抗体情况也是如此。