Dopatka H D, Majer M, Hennessen W, Mauler R
Dev Biol Stand. 1977;38:359-62.
Guinea pigs of inbred strain 2 were vaccinated with BCG 1331 Copenhagen (K-Nr. 240-1) six to seven weeks before intradermal application of about 10(5) leukocytes from a highly leukemic animal in mixture with 10(7) colony forming units (CFU) of BCG. This presensitization with BCG totally abolished or strongly reduced the antitumor activity of L2C-cells adjoining BCG. Increase of bacterial mass applied from 1 X 10(7) to 2 X 10(8) CFU did not restore the antileukemic effect of BCG as observed in unvaccinated guinea pigs by a significant delay of death in a portion of animals and by the occurrence of long-term survivors. Since local reaction to BCG occurred much earlier in presensitized than in unvaccinated animals, we speculate that the destruction of tumor cells and hence the antigenic stimulus was too premature in presensitized animals to build up a BCG-mediated antitumor immunity.
在向近交2系豚鼠皮内注射约10⁵个来自高度白血病动物的白细胞与10⁷个卡介苗集落形成单位(CFU)的混合物前六至七周,用卡介苗1331哥本哈根株(K编号240 - 1)对其进行免疫接种。这种卡介苗预致敏完全消除或显著降低了毗邻卡介苗的L2C细胞的抗肿瘤活性。将接种的细菌量从1×10⁷CFU增加到2×10⁸CFU,并未像在未接种的豚鼠中观察到的那样,通过部分动物死亡的显著延迟和长期存活者的出现来恢复卡介苗的抗白血病作用。由于预致敏动物中对卡介苗的局部反应比未接种动物早得多,我们推测在预致敏动物中肿瘤细胞的破坏以及因此产生的抗原刺激过早,以至于无法建立卡介苗介导的抗肿瘤免疫。