Pullyblank A M, Guillou P J, Monson J R
Academic Surgical Unit, Imperial College of Science, Technology and Medicine, St. Mary's Hospital, London, UK.
Br J Cancer. 1995 Sep;72(3):601-6. doi: 10.1038/bjc.1995.380.
Antibodies are thought to bring about tumour cell lysis by antibody-dependent cell-mediated cytotoxicity (ADCC), but the exact mechanism is not well elucidated. Monocytes are known to be important mediators of anti-tumour ADCC and are also known to secrete the cytokines tumour necrosis factor alpha (TNF-alpha) and interleukin 1 beta (IL-1 beta), both of which have been shown to bring about tumour cell lysis. We examined the release of these cytokines during ADCC and attempted to elucidate which components of the ADCC reaction were necessary for cytokine production. We measured TNF-alpha and IL-1 beta in supernatants collected from a standard ADCC assay using each of the anti-colorectal antibodies m17-1A, c17-1A and cSF25. We found that there was significant TNF-alpha and IL-1 beta release during ADCC mediated by each of these three antibodies and that the magnitude of cytokine release seemed to reflect the degree of tumour cell lysis produced by each antibody. Furthermore, we found that effector cells, target cells and a specific anti-tumour antibody were necessary for this to occur. The presence of only some of the components of the reaction or of an irrelevant antibody produced little or no TNF-alpha or IL-1 beta. We conclude that TNF-alpha and IL-1 beta are released when an effector and tumour target cell are united by a specific tumour antibody and that these cytokines may be important in bringing about tumour cell lysis during the ADCC reaction.
抗体被认为通过抗体依赖的细胞介导的细胞毒性作用(ADCC)导致肿瘤细胞裂解,但其确切机制尚未完全阐明。已知单核细胞是抗肿瘤ADCC的重要介质,并且还已知其分泌细胞因子肿瘤坏死因子α(TNF-α)和白细胞介素1β(IL-1β),这两种细胞因子均已被证明可导致肿瘤细胞裂解。我们研究了ADCC过程中这些细胞因子的释放情况,并试图阐明ADCC反应的哪些成分是细胞因子产生所必需的。我们使用抗结直肠癌抗体m17-1A、c17-1A和cSF25,在标准ADCC试验收集的上清液中测量了TNF-α和IL-1β。我们发现,这三种抗体介导的ADCC过程中均有显著的TNF-α和IL-1β释放,并且细胞因子释放的程度似乎反映了每种抗体产生的肿瘤细胞裂解程度。此外,我们发现效应细胞、靶细胞和特异性抗肿瘤抗体是发生这种情况所必需的。仅存在反应的某些成分或无关抗体时,几乎不会产生或不产生TNF-α或IL-1β。我们得出结论,当效应细胞和肿瘤靶细胞通过特异性肿瘤抗体结合时,TNF-α和IL-1β会释放,并且这些细胞因子在ADCC反应过程中导致肿瘤细胞裂解可能很重要。