Carpentier A F, Chen L, Maltonti F, Delattre J Y
Fédération de neurologie Mazarin et INSERM U 495, Hôpital de la Pitié-Salpêtrière, Paris, France.
Cancer Res. 1999 Nov 1;59(21):5429-32.
Phosphorothioate oligodeoxynucleotides with CpG motifs (CpG-ODNs) activate various immune cell subsets and induce production of numerous cytokines. To evaluate whether CpG-ODNs can induce rejection of established malignant tumor, A/J mice were challenged by the s.c. implantation of a syngenic neuroblastoma cell line (neuro2a) and subsequently injected with CpG-ODNs in the vicinity of the tumor. Daily injections of 10 microg CpG-ODNs for 15 days seemed to be the most potent regimen, leading to the eradication of 5-mm-diameter tumors in one-half of the animals and a significant tumor growth inhibition when compared with controls (88% reduction volume; P<0.001). CpG-ODN-cured animals were further protected against a new tumor challenge. The antitumoral effect of CpG-ODNs was dependent on CpG motifs, and natural killer cells seemed to play a critical role in tumor rejection. We conclude that immunostimulatory CpG-ODNs may induce the rejection of established tumors and warrant further evaluation as a potential immunotherapeutic agent.
带有CpG基序的硫代磷酸酯寡脱氧核苷酸(CpG-ODN)可激活多种免疫细胞亚群并诱导多种细胞因子的产生。为了评估CpG-ODN是否能够诱导已形成的恶性肿瘤发生排斥反应,将同基因神经母细胞瘤细胞系(Neuro2a)皮下植入A/J小鼠体内,随后在肿瘤附近注射CpG-ODN。每天注射10μg CpG-ODN,持续15天似乎是最有效的方案,导致一半的动物体内直径5mm的肿瘤被根除,与对照组相比肿瘤生长受到显著抑制(体积减少88%;P<0.001)。经CpG-ODN治愈的动物对新的肿瘤攻击具有进一步的抵抗力。CpG-ODN的抗肿瘤作用依赖于CpG基序,自然杀伤细胞似乎在肿瘤排斥中起关键作用。我们得出结论,免疫刺激性CpG-ODN可能诱导已形成肿瘤的排斥反应,作为一种潜在的免疫治疗剂值得进一步评估。