Platzer C, Richter G, Uberla K, Hock H, Diamantstein T, Blankenstein T
Institute of Immunology, Klinikum Steglitz, Free University Berlin, FRG.
Eur J Immunol. 1992 Jul;22(7):1729-33. doi: 10.1002/eji.1830220710.
The molecular events during the anti-tumor response induced by interleukin (IL)-4 were investigated by quantitative polymerase chain reaction. The growth of Chinese hamster ovary cells transfected to produce IL-4 (CHO.T1) was strongly suppressed when cells were injected intraperitoneally into nude mice and this suppression was accompanied by the rapid accumulation of activated macrophages. Peritoneal cells from such mice were analyzed for mRNA induced by IL-4. Correlating with a high local IL-4 concentration, several transcripts were found to be up-regulated during the early phase of the anti-tumor response [IL-4 receptor, IL-5, tumor necrosis factor (TNF) and interferon (IFN)-gamma]. The functional relevance of the elevated mRNA levels was analyzed by injection of CHO.T1 cells together with anti-cytokine monoclonal antibodies (mAb). In contrast to anti-IL-5 and anti-TNF mAb, an anti-IFN-gamma mAb interfered with the anti-tumor response demonstrating the involvement of IFN-gamma during the IL-4-induced tumor suppression. Tumor growth in anti-IFN-gamma mAb-treated animals was significantly delayed in comparison to anti-IL-4 mAb-treated mice, suggesting that IFN-gamma-independent effector cells may also be involved.
通过定量聚合酶链反应研究了白细胞介素(IL)-4诱导的抗肿瘤反应过程中的分子事件。当将转染产生IL-4的中国仓鼠卵巢细胞(CHO.T1)腹腔注射到裸鼠体内时,其生长受到强烈抑制,并且这种抑制伴随着活化巨噬细胞的快速积累。分析了此类小鼠的腹膜细胞中由IL-4诱导的mRNA。与高局部IL-4浓度相关,发现在抗肿瘤反应的早期阶段有几种转录物上调[IL-4受体、IL-5、肿瘤坏死因子(TNF)和干扰素(IFN)-γ]。通过将CHO.T1细胞与抗细胞因子单克隆抗体(mAb)一起注射来分析mRNA水平升高的功能相关性。与抗IL-5和抗TNF mAb相反,抗IFN-γ mAb干扰了抗肿瘤反应,表明IFN-γ参与了IL-4诱导的肿瘤抑制过程。与抗IL-4 mAb处理的小鼠相比,抗IFN-γ mAb处理的动物的肿瘤生长明显延迟,这表明可能也涉及不依赖IFN-γ的效应细胞。