Chen Y H, Heller P
Clin Exp Immunol. 1982 Nov;50(2):366-73.
Spleens of BALB/c mice with plasmacytoma contain macrophages (M phi) which were found to suppress the in vitro immune function of normal splenic cells through a diffusible factor. The suppressor activity of these macrophages was reversibly inhibited by ligands specific for the corresponding PC globulin, but not by anti-idiotypic antibody. Anti-idiotypic antibody with complement, however, abrogated the suppressor function, presumably by cytotoxicity. Anti-isotype with complement was ineffective. These findings suggest binding of ligand to a surface receptor of the suppressor M phi that although clearly not PC globulin, may be structurally similar to the PC idiotype. These receptors are retained in 3 day cultures of macrophages and are not removed by intensive washing. Ligand binding appears to modulate the suppressor function of M phi through blocking of the production of diffusible suppressor factor.
患有浆细胞瘤的BALB/c小鼠的脾脏含有巨噬细胞(M phi),发现这些巨噬细胞通过一种可扩散因子抑制正常脾细胞的体外免疫功能。这些巨噬细胞的抑制活性可被相应PC球蛋白的特异性配体可逆性抑制,但不能被抗独特型抗体抑制。然而,具有补体的抗独特型抗体可消除抑制功能,推测是通过细胞毒性作用。具有补体的抗同种型抗体则无效。这些发现表明配体与抑制性M phi的表面受体结合,该受体虽然显然不是PC球蛋白,但在结构上可能与PC独特型相似。这些受体在巨噬细胞的3天培养物中得以保留,且不会因大量洗涤而去除。配体结合似乎通过阻断可扩散抑制因子的产生来调节M phi的抑制功能。