Ranlov P, Hardt F
Clin Exp Immunol. 1971 Feb;8(2):163-71.
A modification of the macrophage or leucocyte migration inhibition assay usable in a murine model has been developed. The system operates with mixed spleen–thymus cell populations from mice sensitized to soluble protein or to transplantation antigens. In order to obtain significant inhibition it was found necessary to preincubate the sensitized cells with specific antigen for 24 hr prior to the migration assay. The macrophage inhibitory factor (MIF) has been found to determine the rate of migration inhibition in the mouse system whereas the role of humoral antibody is negligible. The murine MIF is not strain specific and operates in the absence of specific antigen. Spleen–thymus cells from St/a mice sensitized to a first set C3H skin allograft were inhibited by approximately 30% while cells sensitized to a second set graft showed a 50% inhibition when migrating against C3H cells or MIF produced by confrontation between sensitized St/a lymphoid cells and C3H antigen.
已开发出一种可用于小鼠模型的巨噬细胞或白细胞迁移抑制试验的改良方法。该系统使用来自对可溶性蛋白质或移植抗原致敏的小鼠的混合脾-胸腺细胞群体。为了获得显著的抑制作用,发现有必要在迁移试验前将致敏细胞与特异性抗原预孵育24小时。已发现巨噬细胞抑制因子(MIF)决定了小鼠系统中的迁移抑制率,而体液抗体的作用可忽略不计。小鼠MIF不是品系特异性的,且在没有特异性抗原的情况下也能发挥作用。对初次移植的C3H皮肤同种异体移植物致敏的St/a小鼠的脾-胸腺细胞在与C3H细胞或致敏的St/a淋巴细胞与C3H抗原相互作用产生的MIF迁移时,受到约30%的抑制,而对二次移植致敏的细胞则表现出50%的抑制。