Sonnenfeld G, Mandel A D, Merigan T C
Immunology. 1979 Apr;36(4):883-90.
Antigen-specific type II interferon was produced in vitro by harvesting supernatants of spleen cell cultures from Swiss-Webster mice sensitized with Mycobacterium bovis strain BCG and challenged with old tuberculin. Treatment of C3H mouse spleen cell cultures with appropriate anti-Ia, anti-IgG, anti-Thy-1 or anti-Ly-2,3 sera resulted in a significant decrease in production of type II interferon. Removal of nylon wool adherent cells or cells with histamine receptors by column chromatography similarly caused reduced production of type II interferon. Recombination of spleen cell cultures treated with anti-Ia and anti-Thy-1 sera or of cells treated with anti-IgG and anti-Thy-1 resulted in restored production of type II interferon. Interferon production was also restored by combination of cells passed through histamine columns with anti-Ia treated cells, or those passed through nylon wool columns with anti-Thy-1 treated cells. Anti-Ly-1 serum treatment had no effect on interferon production. Removal of plastic-adherent cells or cells that had phagocytosed carbonyl iron also decreased interferon production, suggesting that macrophages were also involved in type II interferon production. Recombination of non-adherent spleen cells with anti-Ia and anti-Thy-1 sera treated spleen cells, however, did not restore interferon production, suggesting that other cells in addition to macrophages are depleted by the adherence procedure. These findings indicate that type II interferon is produced by suppressor or cytotoxic (Ly-2,3+) T lymphocytes in co-operation with one or two additional cell types: (i) B lymphocytes, and (ii) macrophages.
通过收集用卡介苗牛分枝杆菌菌株致敏并用旧结核菌素攻击的瑞士-韦伯斯特小鼠脾细胞培养物的上清液,在体外产生抗原特异性II型干扰素。用适当的抗Ia、抗IgG、抗Thy-1或抗Ly-2,3血清处理C3H小鼠脾细胞培养物,导致II型干扰素的产生显著减少。通过柱色谱去除尼龙毛贴壁细胞或具有组胺受体的细胞,同样导致II型干扰素的产生减少。用抗Ia和抗Thy-1血清处理的脾细胞培养物或用抗IgG和抗Thy-1处理的细胞进行重组,导致II型干扰素的产生恢复。通过将通过组胺柱的细胞与抗Ia处理的细胞组合,或通过尼龙毛柱的细胞与抗Thy-1处理的细胞组合,也恢复了干扰素的产生。抗Ly-1血清处理对干扰素的产生没有影响。去除塑料贴壁细胞或吞噬了羰基铁的细胞也会降低干扰素的产生,这表明巨噬细胞也参与了II型干扰素的产生。然而,将非贴壁脾细胞与抗Ia和抗Thy-1血清处理的脾细胞重组,并没有恢复干扰素的产生,这表明除巨噬细胞外的其他细胞在贴壁过程中被耗尽。这些发现表明,II型干扰素是由抑制性或细胞毒性(Ly-2,3+)T淋巴细胞与另外一种或两种细胞类型合作产生的:(i)B淋巴细胞,和(ii)巨噬细胞。