Yonkosky D, Buffett R F, Bennett M
J Immunol. 1976 Jun;116(6):1688-94.
A cellfree extract prepared from the spleen cells of C3H mice is capable of suppressing antibody responses to SRBC when extract material is exposed to alloantigens. The observed immunosuppression was attributed to a soluble factor in the extract. This allogeneic suppressive factor (ASF) was detected in extracts prepared from the spleen cells of unirradiated mice as well as those of irradiated mice repopulated with thymocytes, provided that mice were previously immunized with SRBC. Donors of actively suppressive ASF preparations did not need to be previously exposed to alloantigens. Extracts from thymus and marrow cells of unirradiated mice and the spleen cells of irradiated mice repopulated with marrow cells (or no cells) did not contain ASF. C3H thymocytes stimulated with SRBC generated more ASF activity in spleens of C3BF1 hosts than in those of C3H hosts, indicating that alloantigenic stimulation enhances the production or activity of ASF. Once produced, C3H ASF was able to suppress antibody responses in cell transfer experiments only if exposed to C3BF alloantigens of either donor lymphoid cells or irradiated hosts. Once exposed to alloantigens, ASF appears to be capable of suppressing antibody responses of syngeneic C3H or semi-allogeneic C3BF cells. When both donor lymphoid cells and hosts were syngeneic with the donor of the ASF, there was enhancement of antibody formation in cell transfer experiments. C3H ASF did not interfere with education of C3BF thymocytes to SRBC or with the generation of precursors of anti-SRBC antibody-forming cells by C3BF1 marrow cells. ASF may interfere with cellular cooperative events necessary for humoral immune responses or with terminal differentiation of B cells. Production of ASF could partially account for the suppression of antibody responses observed during graft-vs-host reactions.
从C3H小鼠脾细胞制备的无细胞提取物,当提取物材料暴露于同种异体抗原时,能够抑制对绵羊红细胞(SRBC)的抗体反应。观察到的免疫抑制归因于提取物中的一种可溶性因子。这种同种异体抑制因子(ASF)在未照射小鼠以及用胸腺细胞重新填充的照射小鼠的脾细胞提取物中均被检测到,前提是小鼠先前已用SRBC免疫。具有活性抑制作用的ASF制剂的供体无需预先暴露于同种异体抗原。未照射小鼠的胸腺和骨髓细胞提取物以及用骨髓细胞(或无细胞)重新填充的照射小鼠的脾细胞提取物中不含有ASF。用SRBC刺激的C3H胸腺细胞在C3BF1宿主的脾脏中产生的ASF活性比在C3H宿主的脾脏中更多,这表明同种异体抗原刺激增强了ASF的产生或活性。一旦产生,C3H ASF仅在暴露于供体淋巴细胞或照射宿主的C3BF同种异体抗原时,才能在细胞转移实验中抑制抗体反应。一旦暴露于同种异体抗原,ASF似乎能够抑制同基因C3H或半同种异体C3BF细胞的抗体反应。当供体淋巴细胞和宿主与ASF供体同基因时,在细胞转移实验中抗体形成增强。C3H ASF不干扰C3BF胸腺细胞对SRBC的致敏,也不干扰C3BF1骨髓细胞产生抗SRBC抗体形成细胞的前体。ASF可能干扰体液免疫反应所需的细胞协同事件或B细胞的终末分化。ASF的产生可能部分解释了在移植物抗宿主反应期间观察到的抗体反应抑制现象。