Suzuki T, Miyama-Inaba M, Masuda T, Uchino H, Murakami A, Tanaka H
Immunology. 1983 Sep;50(1):149-57.
B cells that have receptors for the Fc portion of IgG (FcR gamma + B cell) elaborate an immunoregulatory lymphokine termed suppressive B-cell factor (SBF) after binding immune complexes, such as sheep erythrocytes sensitized with IgG anti-sheep erythrocyte antibody (EA). For producing SBF, de novo protein is required, but not DNA or DNA-dependent RNA synthesis. This mediator is released into the culture supernatant of FcR gamma + B cells during 6 to 48 hr after stimulation by EA. SBF suppresses the proliferation of B, but not non-B cells. Thus, it suppressed (i) plaque-forming cell responses in the induction phase in an antigen-non-specific manner, (ii) DNA synthesis of lipopolysaccharide-activated B cells, but neither concanavalin A nor phytohaemagglutinin-activated T cells, and (iii) the proliferation of B but not non-B tumour-cell lines by acting at the G1-S junction in the cell cycle. Concordance of H-2 haplotype between SBF-producing mice and target B cells is necessary for the suppression. Thus, the action of SBF is B-cell specific and antigen-non-specific. Immune complex-mediated negative feedback regulation seems to be operated by lymphokines such as SBF which may be also involved in the surveillance for B-cell tumours.
具有IgG Fc段受体的B细胞(FcRγ⁺ B细胞)在结合免疫复合物后,会产生一种称为抑制性B细胞因子(SBF)的免疫调节性淋巴因子,所述免疫复合物如用IgG抗绵羊红细胞抗体(EA)致敏的绵羊红细胞。为了产生SBF,需要重新合成蛋白质,但不需要DNA或依赖DNA的RNA合成。在被EA刺激后的6至48小时内,这种介质会释放到FcRγ⁺ B细胞的培养上清液中。SBF可抑制B细胞而非非B细胞的增殖。因此,它能以抗原非特异性的方式抑制:(i)诱导期的空斑形成细胞反应;(ii)脂多糖激活的B细胞的DNA合成,但对刀豆球蛋白A或植物血凝素激活的T细胞无抑制作用;以及(iii)通过作用于细胞周期的G1-S期交界处,抑制B肿瘤细胞系而非非B肿瘤细胞系的增殖。产生SBF的小鼠与靶B细胞之间的H-2单倍型一致是抑制作用所必需的。因此,SBF的作用具有B细胞特异性且抗原非特异性。免疫复合物介导的负反馈调节似乎是由诸如SBF之类的淋巴因子所介导的,其可能也参与了对B细胞肿瘤的监测。