Ptak W, Zembala M, Asherson G L, Marcinkiewicz J
Int Arch Allergy Appl Immunol. 1981;65(2):121-8. doi: 10.1159/000232747.
Lymphoid cells of mice injected with picrylsulphonic acid and then painted with picryl chloride produce a specific T suppressor factor (TSF) in vitro. This factor arms peritoneal exudate cells, which then produce a nonspecific factor which inhibits the transfer of contact sensitivity by immune cells incubated in it. An adherent, theta-negative cell, which is presumably a macrophage, is responsible. This justifies the use of the term macrophage suppressor factor. As a separate phenomenon, passive transfer cells lose their activity when incubated on high density monolayers of normal peritoneal exudate cells. However, this is not associated with the production of a supernatant factor. The inhibition of transfer when immune cells are incubated with specific TSF is unaffected by nylon wool filtration (which removes macrophages). This suggests that TSF is able to depress the passive transfer of contact sensitivity by a macrophage-independent process.
给小鼠注射苦味磺酸,然后用苦味酰氯涂抹,其淋巴细胞在体外可产生一种特异性T抑制因子(TSF)。该因子武装腹膜渗出细胞,后者进而产生一种非特异性因子,该因子可抑制在其中孵育的免疫细胞传递接触敏感性。一种贴壁的、θ阴性细胞(可能是巨噬细胞)起作用。这证明了使用巨噬细胞抑制因子这一术语的合理性。作为一种单独的现象,被动转移细胞在正常腹膜渗出细胞的高密度单层上孵育时会失去活性。然而,这与上清因子的产生无关。免疫细胞与特异性TSF一起孵育时转移的抑制不受尼龙毛过滤(可去除巨噬细胞)的影响。这表明TSF能够通过一种不依赖巨噬细胞的过程抑制接触敏感性的被动转移。