Zhang Sheng, Wang Qin, Li Wen-Feng, Wang Hong-Yi, Zhang Hong-Jun
Department of Medical Oncology, Medical School Hospital of Qingdao University, 16 Jiangsulu, Qingdao, China.
Leuk Res. 2004 Oct;28(10):1085-8. doi: 10.1016/j.leukres.2004.01.014.
Human cytokine induced killer cells (CIK) have shown potent non-major histocompatibility (MHC)-restricted antitumor activity in vitro in recent years. Using a similar protocol, we generated murine cytokine activated T lymphocytes (CAT) from splenocytes with the sequential addition of IFN-gamma, IL-1beta, anti-CD3 and IL-2. The NK depleted CATs did not possess significant antitumor activity both in vitro and in vivo. However, after cocultured with dendritic cells (DC) pulsed with whole tumor lysates, significant specific antitumor activity was observed both in vitro and in vivo. Our data demonstrated that the CATs cocultured with dendritic cells pulsed with whole tumor lysates have potent specific antitumor effects and might be useful in the treatment of malignancies.
近年来,人细胞因子诱导杀伤细胞(CIK)在体外已显示出强大的非主要组织相容性复合体(MHC)限制的抗肿瘤活性。采用类似方案,我们通过依次添加干扰素-γ、白细胞介素-1β、抗CD3和白细胞介素-2,从脾细胞中生成了鼠细胞因子活化T淋巴细胞(CAT)。去除自然杀伤细胞的CAT在体外和体内均不具有显著的抗肿瘤活性。然而,在用全肿瘤裂解物脉冲处理的树突状细胞(DC)共培养后,在体外和体内均观察到显著的特异性抗肿瘤活性。我们的数据表明,与用全肿瘤裂解物脉冲处理的树突状细胞共培养的CAT具有强大的特异性抗肿瘤作用,可能对恶性肿瘤的治疗有用。