Douglas G N, Rubin A S
Immunology. 1977 Nov;33(5):745-55.
Specific anamnestic stimulation of spleen cells from mice immunized 7 days earlier with horse erythrocytes (HRBC) generated the release of a soluble factor that was capable of suppressing the initiation of the in vitro primary gammaM immune response to sheep red blood cells (SRBC), as well as to the immunogen that elicited its formation. Moreover, the suppressive macromolecule (mol. wt yields to 34,000), derived from antigen-activated, HRBC-primed T lymphocytes (but not B cells), inhibited the secondary gammaM and gammaG anti-SRBC plaque-forming cell responses of SRBC-primed spleen cells. The active material was resistant to treatment with DNase and RNase, but was inactivated by protease (10 microgram/ml, 30 min) or exposure to mild heat (56 degrees, 30 min). The antibody initiation suppressor factor (AISF) was concentrated and partially purified by gel filtration, followed by poly-acrylamide gel electrophoresis.
对7天前用马红细胞(HRBC)免疫的小鼠的脾细胞进行特异性回忆性刺激,可产生一种可溶性因子,该因子能够抑制体外对绵羊红细胞(SRBC)以及引发其形成的免疫原的初次γM免疫应答的启动。此外,源自抗原激活的、经HRBC致敏的T淋巴细胞(而非B细胞)的抑制性大分子(分子量为34,000),抑制了经SRBC致敏的脾细胞的二次γM和γG抗SRBC空斑形成细胞应答。活性物质对DNase和RNase处理具有抗性,但可被蛋白酶(10微克/毫升,30分钟)或暴露于温和加热(56摄氏度,30分钟)灭活。抗体启动抑制因子(AISF)通过凝胶过滤,随后进行聚丙烯酰胺凝胶电泳进行浓缩和部分纯化。