Maurer B A, Dean J H, McCoy J L, Appella E, Law L W
J Natl Cancer Inst. 1976 May;56(5):1075-8. doi: 10.1093/jnci/56.5.1075.
The cell-mediated immune status of B10.D2 (H-2d) mice immunized with spleen cells from a congenic strain, B10.A (H-2a), differing at the H-2 locus and of BALB/c mice immunized with a syngeneic simian virus 40 (SV40)-induced sarcoma (mKSA-TU5) was evaluated by an agarose microassay for migration inhibition factor. The inducing antigens in this experiment were papain-solubilized and partially purified chromatographic preparations of spleen cells from A/J mice (H-2a) and a papain-solubilized antigen extract prepared from a tissue culture-adapted cell line (TU-5), derived from the SV40-induced mKSA tumor. The assay used microliters of normal or immune peritoneal exudate cells (PEC) resuspended in a 2-mul droplet of agarose and cultured in the presence or absence of antigen. Specific migration inhibition of PEC from immunized mice was observed with concentrations of solubilized antigen preparations as low as 2.0 mug/ml (3.67 mug/chamber).
用来自在H-2位点不同的同基因品系B10.A(H-2a)的脾细胞免疫的B10.D2(H-2d)小鼠以及用同基因猿猴病毒40(SV40)诱导的肉瘤(mKSA-TU5)免疫的BALB/c小鼠的细胞介导免疫状态,通过琼脂糖微量测定法检测迁移抑制因子进行评估。本实验中的诱导抗原是用木瓜蛋白酶溶解并经部分纯化的A/J小鼠(H-2a)脾细胞层析制剂,以及从源自SV40诱导的mKSA肿瘤的组织培养适应细胞系(TU-5)制备的木瓜蛋白酶溶解抗原提取物。该测定使用微升重悬于2微升琼脂糖液滴中的正常或免疫腹膜渗出细胞(PEC),并在有或无抗原的情况下进行培养。用低至2.0微克/毫升(3.67微克/小室)的溶解抗原制剂浓度时,观察到来自免疫小鼠的PEC出现特异性迁移抑制。