Tumour-activated macrophages as effector cells in a tumour neutralization assay in vivo.

R Olstad, G Kaplan, R Seljelid
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Abstract

Macrophages from C3D2 or C57B1/6 mice were activated in vitro by coculture with MC1M-AA sarcoma cells or by addition of cell free tumour ascites fluid from the same tumour. After 5-7 days of in vitro activation, macrophages were harvested, mixed with MC1M-AA or B-16 melanoma cells, and reinjected into C3D2 or C57B1/6 mice respectively. Mice were evaluated for tumour development, and the early histological appearance of the B16 melanomas was studied. Activated macrophages gave a significant delay and decrease in tumour take when mixed with B16 melanoma cells at a tumour cell: activated macrophage ratio of 1:20. When activated macrophages were mixed with MC1M-AA cells at a tumour cell: activated macrophage ratio of 1:50, a slight delay and a significant decrease in tumour take was observed. BCG-activated macrophages did exhibit a very weak effect on MC1M-AA tumour growth. When B16 melanoma cells were injected into mice together with activated macrophages, an acute inflammatory reaction was observed at the site of injection. The organization of the tumour was delayed, and necrotic tumour cells could be found. In some cases, small islands of tumour cells escaped killing, and gave rise to delayed tumour development.

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肿瘤活化巨噬细胞在体内肿瘤中和试验中的效应细胞。
C3D2或C57B1/6小鼠巨噬细胞通过与MC1M-AA肉瘤细胞共培养或添加来自同一肿瘤的无细胞肿瘤腹水在体外活化。体外活化5-7天后,收集巨噬细胞,与MC1M-AA或B-16黑色素瘤细胞混合,分别回注射到C3D2或C57B1/6小鼠体内。评估小鼠肿瘤的发展,并研究了B16黑色素瘤的早期组织学外观。活化的巨噬细胞与B16黑色素瘤细胞混合,肿瘤细胞与活化的巨噬细胞的比例为1:20,可显著延缓和减少肿瘤的发生。将活化的巨噬细胞与MC1M-AA细胞按肿瘤细胞:活化的巨噬细胞比例1:50混合后,观察到肿瘤体积略有延迟且明显减小。bcg激活的巨噬细胞对MC1M-AA肿瘤生长的影响非常微弱。当B16黑色素瘤细胞与活化的巨噬细胞一起注射到小鼠体内时,在注射部位观察到急性炎症反应。肿瘤组织延迟,可见坏死的肿瘤细胞。在某些情况下,肿瘤细胞的小岛屿逃脱了杀戮,并导致肿瘤发展延迟。
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