Suslov A P, Egorova S G, Brondz B D
Biull Eksp Biol Med. 1975 Oct;80(10):86-90.
High immunological specificity of the direct and indirect macrophage migration inhibition tests was demonstrated in the H-2 system. The capacity of immune lymphocytes for the MIF production was revealed under their incubation with splenic cells of the congenic or recombinant strains of mice sharing particular private or public H-2 specificities with the donor strains. Selective removal of cytotoxic fraction of lymphocytes resulting from their absorption on the corresponding target cells failed to reduce the capacity of the non-adherent cell population for the MIF production. A fraction of the MIF-producing lymphocytes was found to adhere to the target cells and thereafter to be eluated with the cytotoxic lymphocytes. MIF-producing and target-destroying T-lymphocyte populations are supposed to have antigen-binding receptors differing in their affinity and structural arrangement on the cell surface.
在H-2系统中证明了直接和间接巨噬细胞移动抑制试验具有高度免疫特异性。当免疫淋巴细胞与与供体品系具有特定私有或公共H-2特异性的同基因或重组品系小鼠的脾细胞一起孵育时,显示出免疫淋巴细胞产生巨噬细胞移动抑制因子(MIF)的能力。淋巴细胞的细胞毒性部分通过在相应靶细胞上的吸附而被选择性去除,这并未降低非贴壁细胞群体产生MIF的能力。发现一部分产生MIF的淋巴细胞粘附于靶细胞,随后与细胞毒性淋巴细胞一起被洗脱。产生MIF和破坏靶细胞的T淋巴细胞群体被认为在细胞表面具有亲和力和结构排列不同的抗原结合受体。