Nakamura Y, Tokuda Y, Iwasawa M, Tsukamoto H, Kidokoro M, Kobayashi N, Kato S, Mitomi T, Habu S, Nishimura T
Blood Transfusion Service Center, Tokai University School of Medicine, Isehara, Japan.
Br J Cancer. 1992 Jul;66(1):20-6. doi: 10.1038/bjc.1992.210.
A simple method for the rapid expansion of human CD4+ T cells with both helper and killer functions was established. CD4+ T cells separated from peripheral blood mononuclear cells using immunomagnetic beads were stimulated with immobilised OKT-3 monoclonal antibody (mAb) plus recombinant interleukin 2 (rIL-2) in 96 well culture plates. After 6 day-culture, the CD4+ T cells were restimulated by immobilised OKT-3 mAb for an additional 24 h, then inoculated into concentrated rotary-tissue culture bag and cultured for further 9 days. This procedure yielded a 3000-fold increase in cell number (about 3-5 x 10(9) per bag). Most of the cells (over 96%) continued to express CD4+ antigen and retained their capacity to produce IL-2. The activated CD4+ T cells showed marked cytotoxicity against Fc receptor positive tumour cells in the presence of OKT-3 mAb. Moreover, we succeeded in a specific targeting of the expanded CD4+ helper/killer T cells to c-erb B-2 positive tumour cells by means of anti-CD3 x anti-c-erb B-2 bispecific antibody. These results suggested that our established simple system will be available for the expansion of large number of CD4+ helper/killer T cells which may provide an efficient strategy for adoptive tumour immunotherapy.
建立了一种快速扩增具有辅助和杀伤功能的人CD4+T细胞的简单方法。使用免疫磁珠从外周血单个核细胞中分离出的CD4+T细胞,在96孔培养板中用固定化的OKT-3单克隆抗体(mAb)加重组白细胞介素2(rIL-2)进行刺激。培养6天后,用固定化的OKT-3 mAb再次刺激CD4+T细胞24小时,然后接种到浓缩旋转组织培养袋中再培养9天。该程序使细胞数量增加了3000倍(每袋约3-5×10^9个)。大多数细胞(超过96%)继续表达CD4+抗原并保留产生IL-2的能力。在OKT-3 mAb存在的情况下,活化的CD4+T细胞对Fc受体阳性肿瘤细胞显示出明显的细胞毒性。此外,我们通过抗CD3×抗c-erb B-2双特异性抗体成功地将扩增的CD4+辅助/杀伤性T细胞特异性靶向c-erb B-2阳性肿瘤细胞。这些结果表明,我们建立的简单系统可用于大量扩增CD4+辅助/杀伤性T细胞,这可能为过继性肿瘤免疫治疗提供一种有效的策略。