Deutsch O, Devens B, Naor D
Isr J Med Sci. 1980 Jul;16(7):530-7.
YAC, a Moloney-virus-induced tumor of A mice, caused an inhibition of specific immunologic responses in A and C57BL/6 mice, which was mediated by suppressor cells. In contrast, YAC-1, the in vitro-carried tumor derived from cultivated YAC cells, stimulated the appearance of antitumor reactive cells in A mice. Splenocytes from YAC-1-injected mice generated anti-YAC cytotoxic cells after six days of culture. The suppressor cells from YAC-injected mice efficiently inhibited the cytotoxic responses of the cultivated reactive cells (YAC-1-primed cells) when added at the start of the culture, but not when added at later times. Suppressor cells appeared in A mice three days after injecion of YAC cells and persisted in the animals for at least 50 days. YAC-1-primed cells, derived from A mice 1, 3, 9 and 20 days after injection of YAC-1 cells, were sensitive to the suppressor cells.
YAC是一种莫洛尼病毒诱导的A系小鼠肿瘤,它会抑制A系和C57BL/6系小鼠的特异性免疫反应,这种抑制作用由抑制性细胞介导。相比之下,YAC-1是源自培养的YAC细胞的体外携带肿瘤,它能刺激A系小鼠中抗肿瘤反应性细胞的出现。注射YAC-1的小鼠的脾细胞在培养六天后产生抗YAC细胞毒性细胞。来自注射YAC的小鼠的抑制性细胞在培养开始时添加时能有效抑制培养的反应性细胞(YAC-1致敏细胞)的细胞毒性反应,但在后期添加时则不能。抑制性细胞在注射YAC细胞三天后出现在A系小鼠中,并在动物体内持续至少50天。在注射YAC-1细胞后1、3、9和20天从A系小鼠获得的YAC-1致敏细胞对抑制性细胞敏感。