Sone S, Utsugi T, Nii A, Ogura T
J Immunol. 1987 Jul 1;139(1):29-34.
Normal human alveolar macrophages (AM) significantly and reproducibly suppress induction of IL 2-activated killer (LAK) cell activity against allogeneic Burkitt's lymphoma (Daudi) cells. Incubation of purified peripheral blood lymphocytes for 4 days with autologous AM and 1 U/ml of IL 2 resulted in AM-mediated suppression of LAK activity, whereas peripheral blood monocytes isolated freshly by centrifugal elutriation from the same donor potentiated induction of LAK activity by IL 2. The suppression of LAK cell induction by human AM was dependent on the density of AM added to the lymphocyte cultures. Recombinant IFN-gamma did not affect AM-mediated suppression of LAK cell induction by IL 2. Both AM and monocytes stimulated with lipopolysaccharide markedly suppressed LAK cell induction by IL 2. AM-mediated down-regulation was seen only when AM were added immediately after the start of incubation of lymphocytes with IL 2; AM potentiated LAK activity when added 1 day later. Similar AM-mediated suppression of LAK cell induction was observed with four lines of allogeneic lung cancer cells as targets for LAK activity. These results indicate that AM may be important in regulation of in situ induction of LAK activity in the lung.
正常人肺泡巨噬细胞(AM)能显著且可重复地抑制白细胞介素2激活的杀伤细胞(LAK)对同种异体伯基特淋巴瘤(Daudi)细胞的杀伤活性。将纯化的外周血淋巴细胞与自体AM及1 U/ml白细胞介素2共同孵育4天,可导致AM介导的LAK活性抑制,而通过离心淘洗从同一供体新鲜分离的外周血单核细胞则增强白细胞介素2对LAK活性的诱导。人AM对LAK细胞诱导的抑制作用取决于添加到淋巴细胞培养物中的AM密度。重组干扰素-γ并不影响AM介导的白细胞介素2对LAK细胞诱导的抑制作用。脂多糖刺激的AM和单核细胞均显著抑制白细胞介素2对LAK细胞的诱导。只有在淋巴细胞与白细胞介素2开始孵育后立即添加AM时,才会出现AM介导的下调作用;1天后添加AM则增强LAK活性。以四株同种异体肺癌细胞作为LAK活性的靶标时,也观察到了类似的AM介导的LAK细胞诱导抑制作用。这些结果表明,AM可能在肺原位LAK活性诱导的调节中起重要作用。