Kim Hwan Mook, Kang Jong Soon, Lim Jaeseung, Park Song-Kyu, Lee Kiho, Yoon Yeo Dae, Lee Chang Woo, Lee Ki Hoon, Han Gyoonhee, Yang Kyu-Hwan, Kim Yeon Jin, Kim Youngsoo, Han Sang-Bae
Bioevaluation Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Ochang, Chungbuk 363-883, Korea.
Arch Pharm Res. 2007 Nov;30(11):1464-70. doi: 10.1007/BF02977372.
Despite the recent improvement in the treatment of ovarian cancer, this disease is still leading cause of cancer death in women. In this study, the anti-tumor activity of cytokine-induced killer (CIK) cells against human ovarian cancer was evaluated in vitro and in vivo. Although CD3+CD56+ cells were rare in fresh human peripheral blood mononuclear cells, they could expand more than 1,000-fold on day 14 in the presence of anti-CD3 antibody plus IL-2. At an effector-target cell ratio of 30:1, CIK cells destroyed 45% of SK-OV-3 human ovarian cancer cells, which was determined by the 51Cr-release assay. In addition, CIK cells at a dose of 23 million cells per mouse inhibited 73% of SK-OV-3 tumor growth in nude mouse xenograft assay. This study suggests that CIK cells may be used as an adoptive immunotherapy for patients with ovarian cancer.
尽管近期卵巢癌的治疗有所改善,但这种疾病仍是女性癌症死亡的主要原因。在本研究中,对细胞因子诱导的杀伤(CIK)细胞针对人卵巢癌的抗肿瘤活性进行了体内和体外评估。虽然新鲜人外周血单个核细胞中CD3 + CD56 +细胞很少见,但在抗CD3抗体加IL-2存在的情况下,它们在第14天可扩增超过1000倍。在效应细胞与靶细胞比例为30:1时,CIK细胞破坏了45%的SK-OV-3人卵巢癌细胞,这是通过51Cr释放试验确定的。此外,在裸鼠异种移植试验中,每只小鼠注射2300万个细胞剂量的CIK细胞抑制了73%的SK-OV-3肿瘤生长。本研究表明,CIK细胞可用作卵巢癌患者的过继性免疫疗法。