Herscowitz H B, Pennline K J, Conrad R E, Ullrich S E, Gerber H R
Ann N Y Acad Sci. 1979;332:464-81. doi: 10.1111/j.1749-6632.1979.tb47141.x.
Adherent-cell-depleted primed rabbit splenocytes were capable of mounting an in vitro response to SRBC. The addition of alveolar macrophages (AM) to adherent-cell-depleted or unseparated lymphoid cell populations resulted in significant suppression of the PFC response. Suppressive activity was limited to AM and dependent on the presence of a ratio of 1 AM:20 lymphocytes. The cell-mediating suppression was found to be resistant to irradiation and antithymus globulin but sensitive to heat, freeze-thawing, and treatment with iodoacetamide. Suppression was mediated by a soluble factor (MW greater than 10,000 daltons) that required an AM-lymphocyte interaction for its production. Suppression appeared to be achieved through the inhibition of proliferation of antigen sensitive cells although the effect of AM could possibly be exerted on an early event in the immune response. AM were capable of enhancing the proliferative responses of rabbit lymphoid cells to PHA and Con A. Enhancing and suppressing activities of AM were abolished by inhibition of RNA synthesis but unaffected by inhibitors of DNA and protein synthesis.
去除贴壁细胞的致敏兔脾细胞能够对绵羊红细胞产生体外反应。将肺泡巨噬细胞(AM)添加到去除贴壁细胞的或未分离的淋巴细胞群体中,会导致对空斑形成细胞(PFC)反应的显著抑制。抑制活性仅限于AM,且依赖于1个AM:20个淋巴细胞的比例。发现介导抑制作用的细胞对辐射和抗胸腺细胞球蛋白具有抗性,但对热、冻融以及碘乙酰胺处理敏感。抑制作用由一种可溶性因子(分子量大于10,000道尔顿)介导,该因子的产生需要AM与淋巴细胞相互作用。抑制作用似乎是通过抑制抗原敏感细胞的增殖来实现的,尽管AM的作用可能施加于免疫反应的早期事件。AM能够增强兔淋巴细胞对PHA和Con A的增殖反应。AM的增强和抑制活性可通过抑制RNA合成而消除,但不受DNA和蛋白质合成抑制剂的影响。