Harada M, Pearson G, Redmon L, Winters E, Kasuga S
J Immunol. 1975 Apr;114(4):1318-22.
The temporal development of antibodies to Moloney sarcoma virus (MSV)-induced antigens in relation to tumor progression was followed with the membrane immunofluorescence (MF) and antibody-dependent normal lymphocyte cytotoxicity (ADNLC) assays. Antibody was detected at 14 days following virus infection by MF. In mice that developed primary tumors which regressed, MF titers developed to high levels following a period between 2 and 4 weeks post-innoculation during which the titers remained at low and constant levels. The increase in MF titers corresponded closely on a temporal basis to the initiation of the regression process. In contrast, antibody remained at low levels in those mice that developed progressively growing tumors. ADNLC was detected in the sera of regressor mice approximately 6 weeks post-inoculation but was not detectable at any of the time interavals in sera from mice with progressively growing tumors. Attempts to enhance the cytotoxic activity of normal spleen cells directly with immune serum were unsuccessful. The synergistic effect of serum on the cytotoxic activity of immune lymphocytes was less pronounced than with normal lymphocytes in this system. Temporal studies indicated that there was an inverse relationship between the development of cellular immunity and the capablility of these cells to be activated in the ADNLC assay.
采用膜免疫荧光(MF)和抗体依赖性正常淋巴细胞细胞毒性(ADNLC)试验,追踪了针对莫洛尼肉瘤病毒(MSV)诱导抗原的抗体随时间的发展与肿瘤进展的关系。通过MF在病毒感染后14天检测到抗体。在发生原发性肿瘤后又消退的小鼠中,MF滴度在接种后2至4周期间保持在低水平且稳定,之后发展到高水平。MF滴度的增加在时间上与消退过程的开始密切相关。相比之下,在那些发生肿瘤持续生长的小鼠中,抗体水平保持在低水平。在接种后约6周,在肿瘤消退小鼠的血清中检测到ADNLC,但在肿瘤持续生长小鼠的血清中,在任何时间间隔均未检测到。试图用免疫血清直接增强正常脾细胞的细胞毒性活性未成功。在该系统中,血清对免疫淋巴细胞细胞毒性活性的协同作用不如对正常淋巴细胞明显。时间研究表明,细胞免疫的发展与这些细胞在ADNLC试验中被激活的能力之间存在负相关关系。