Cameron D J, Churchill W H
J Clin Invest. 1979 May;63(5):977-84. doi: 10.1172/JCI109398.
Human macrophages, derived from peripheral blood monocytes, acquire enhanced cytotoxicity for human target cells after incubation in mediator-rich supernates from antigen-stimulated lymphocytes. Maximum cytotoxicity was observed after 24-h incubation in mediators. In comparison to normal macrophages, mediator-activated macrophages were cytotoxic to five of the six malignant cell lines tested but had no effect on five nonmalignant cell lines. In 20 experiments with one target (SK-BR-3), mean cytotoxicity was 23 +/- 2.7% and with another target (MA-160), was 29 +/- 3.4%. Macrophages became cytotoxic after 8-h incubation with mediators and the enhanced cytotoxicity persisted for at least 40 h after the lymphocyte mediators were removed. These findings are consistent with the hypothesis that macrophages, activated by antigen-induced lymphocyte mediators, can contribute to the host resistance to tumor growth in man.
源自外周血单核细胞的人巨噬细胞,在富含介质的抗原刺激淋巴细胞的上清液中孵育后,对人靶细胞的细胞毒性增强。在介质中孵育24小时后观察到最大细胞毒性。与正常巨噬细胞相比,介质激活的巨噬细胞对所测试的六种恶性细胞系中的五种具有细胞毒性,但对五种非恶性细胞系没有影响。在针对一个靶标(SK-BR-3)的20次实验中,平均细胞毒性为23±2.7%,针对另一个靶标(MA-160)为29±3.4%。巨噬细胞与介质孵育8小时后具有细胞毒性,并且在去除淋巴细胞介质后,增强的细胞毒性持续至少40小时。这些发现与以下假设一致,即由抗原诱导的淋巴细胞介质激活的巨噬细胞可以有助于宿主抵抗人类肿瘤生长。