Schirrmacher V, Rubin B, Pross H, Wigzell H
J Exp Med. 1974 Jan 1;139(1):93-107. doi: 10.1084/jem.139.1.93.
Spleen cells from mice immunized against ovalbumin (OA) or dinitrophenylated mouse serum albumin (DM) were found to be specifically cytotoxic in vitro towards target cells (chicken red blood cells) coated with these antigens. Inhibition of specific cytotoxicity was observed when free soluble antigen was added to the incubation mixtures. DM-immune cell cytotoxicity could be specifically and completely inhibited by DNP-lysine and was thus shown to be hapten specific. Complete and specific inhibition was also observed for OA-immune cell cytotoxicity using OA as inhibitor, but compared with the inhibition curves obtained with DNP-lysine, the OA cytotoxicity inhibition curves were shifted by a factor of about one hundred towards lower molar inhibitor concentrations. Very similar results were observed when the serum antibodies of DM- and OA-immune animals were analyzed by passive hemagglutination inhibition. With increasing time after immunization, both cytotoxicity inhibition curves and agglutination inhibition curves, shifted to lower antigen or hapten concentrations. Specific cytotoxicity against antigen-coated target cells was induced in nonimmune spleen cells (a) by serum from immune animals, and (b) by supernatants from in vitro immune cell cultures. In both instances, the factor which induced antigen-specific cytotoxic activity could be absorbed on anti-mouse Ig columns, thus demonstrating its immunoglobulin nature. The ability of target cell bound antibodies to induce cytotoxicity in nonimmune spleen cells was restricted to the 7S antibody class.
发现用卵清蛋白(OA)或二硝基苯基化小鼠血清白蛋白(DM)免疫的小鼠脾细胞在体外对包被有这些抗原的靶细胞(鸡红细胞)具有特异性细胞毒性。当向孵育混合物中加入游离的可溶性抗原时,可观察到特异性细胞毒性受到抑制。DNP -赖氨酸可特异性且完全抑制DM免疫细胞的细胞毒性,因此表明其具有半抗原特异性。使用OA作为抑制剂时,也观察到对OA免疫细胞细胞毒性的完全和特异性抑制,但与用DNP -赖氨酸获得的抑制曲线相比,OA细胞毒性抑制曲线向较低摩尔抑制剂浓度方向移动了约100倍。当通过被动血凝抑制分析DM免疫和OA免疫动物的血清抗体时,观察到非常相似的结果。随着免疫后时间的增加,细胞毒性抑制曲线和凝集抑制曲线都向较低的抗原或半抗原浓度移动。非免疫脾细胞中针对包被抗原的靶细胞的特异性细胞毒性可通过以下方式诱导:(a)免疫动物的血清,以及(b)体外免疫细胞培养物的上清液。在这两种情况下,诱导抗原特异性细胞毒性活性的因子都可被抗小鼠Ig柱吸附,从而证明其免疫球蛋白性质。靶细胞结合抗体在非免疫脾细胞中诱导细胞毒性的能力仅限于7S抗体类别。