Day M J, Russell J, Kitwood A J, Ponsford M, Elson C J
Department of Pathology, University of Bristol, GB.
Eur J Immunol. 1989 May;19(5):795-801. doi: 10.1002/eji.1830190503.
Mice immunized with intact rat red blood cells (RBC) developed serum auto-antibodies (some of which were mouse specific) to the RBC membrane components spectrin and antigens of 100 and 81 kDa as shown by Western blotting and enzyme-linked immunosorbent assay as well as RBC surface-bound autoantibodies detected by the Coombs' test. In order to discover whether these autoantibodies were induced and controlled in similar or different ways, mice were challenged with a variety of rat and mouse RBC preparations. In addition, the ability of recipients given spleen cells from the above donors to generate autoantibody responses to intact rat RBC was measured. It was found that all the autoantibodies were induced in mice challenged with rat RBC ghosts but none following immunization with butanol-extracted rat RBC ghosts or intact mouse RBC. By contrast, mice injected with mouse RBC ghosts made autoantibodies to spectrin and to the 100-kDa band. Spleen cells from mice primed with intact rat RBC, rat RBC ghosts or butanol-extracted rat RBC ghosts curtailed Coombs' autoantibody production of recipient mice challenged with intact rat RBC. Serum from recipients of spleen cells primed with intact rat RBC or the butanol extract generally failed to react with rat or mouse spectrin or with the 81-kDa band, although antibody was detected to the rat 100-kDa band. Recipients of rat RBC ghost-primed spleen cells produced antibody to rat and mouse spectrin and to rat 100-kDa band but not to mouse 100-kDa or rat or mouse 81-kDa bands. Occasionally, suppression of antibody to the rat-specific 38-kDa band was observed in recipients of intact rat RBC-primed spleen cells. It is therefore suggested that regulation of cross-reactive and mouse-specific autoantibodies as well as rat-specific antibodies occurs in an independent, determinant-specific manner.
用完整大鼠红细胞(RBC)免疫的小鼠产生了针对RBC膜成分血影蛋白以及100 kDa和81 kDa抗原的血清自身抗体(其中一些是小鼠特异性的),这通过蛋白质印迹法、酶联免疫吸附测定法得以证实,同时库姆斯试验也检测到了RBC表面结合的自身抗体。为了探究这些自身抗体是以相似还是不同的方式被诱导和调控的,用多种大鼠和小鼠RBC制剂对小鼠进行了攻击。此外,还检测了接受上述供体脾细胞的受体对完整大鼠RBC产生自身抗体反应的能力。结果发现,在用大鼠RBC空壳攻击的小鼠中诱导产生了所有自身抗体,但在用丁醇提取的大鼠RBC空壳或完整小鼠RBC免疫后均未产生。相比之下,注射小鼠RBC空壳的小鼠产生了针对血影蛋白和100 kDa条带的自身抗体。用完整大鼠RBC、大鼠RBC空壳或丁醇提取的大鼠RBC空壳致敏的小鼠的脾细胞,抑制了用完整大鼠RBC攻击的受体小鼠的库姆斯自身抗体产生。用完整大鼠RBC或丁醇提取物致敏的脾细胞受体的血清通常不能与大鼠或小鼠血影蛋白或81 kDa条带发生反应,尽管检测到了针对大鼠100 kDa条带的抗体。用大鼠RBC空壳致敏的脾细胞受体产生了针对大鼠和小鼠血影蛋白以及大鼠100 kDa条带的抗体,但未产生针对小鼠100 kDa条带或大鼠或小鼠81 kDa条带的抗体。偶尔,在用完整大鼠RBC致敏的脾细胞受体中观察到针对大鼠特异性38 kDa条带的抗体受到抑制。因此,有人提出,交叉反应性和小鼠特异性自身抗体以及大鼠特异性抗体的调节是以独立的、决定簇特异性的方式发生的。