Barton B E
Department of Medicine, Stanford University Medical Center, California 94305.
Cell Immunol. 1988 Sep;115(2):228-45. doi: 10.1016/0008-8749(88)90178-5.
Spleens from 1-day-old DBA/2J mice were fused to the nonsecreting myeloma, FO. Dialyzed supernates of these cells were found to suppress the antigen-specific proliferative response of cloned helper or alloreactive T cells at a final concentration of less than or equal to 5%. The same supernate-containing factor did not suppress the response to IL-2 of an IL-2-addicted T cell line. The factor was found not to suppress the production of either IL-2 or antibody, following stimulation of spleen cells with LPS. Absorption analysis revealed that the target of the factor was the accessory cell population. Further experiments indicated that the factor blocked the proliferation of thymocytes due to IL-1. Biochemical analysis revealed a molecular weight for the factor of about 90,000 and a pI of approximately 4.5.
将1日龄DBA/2J小鼠的脾脏与非分泌性骨髓瘤FO融合。发现这些细胞的透析上清液在终浓度小于或等于5%时可抑制克隆化辅助性T细胞或同种异体反应性T细胞的抗原特异性增殖反应。含有相同上清液的因子并不抑制IL-2依赖型T细胞系对IL-2的反应。在用LPS刺激脾细胞后,发现该因子不抑制IL-2或抗体的产生。吸收分析表明该因子的作用靶点是辅助细胞群体。进一步实验表明该因子可阻断由IL-1引起的胸腺细胞增殖。生化分析显示该因子的分子量约为90,000,等电点约为4.5。