Song Li-Ping, Cheng Ju-Long, Wang Xiang-Bin, Zhang Zhong, Fang Min, Zhou Zhi-Yong, Huang Hua-Liang
Institute of Genetics and Developmental Biology, the Chinese Academy of Sciences, Beijing 100101, China.
Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003 Jun;35(6):503-10.
Bispecific antibodies (BsAb) with specificity to both tumor cells and CD3 molecule were believed to be promising immunological tools for the therapy with minimal residual diseases by activating cytotoxic T cells. However, without costimulatory molecule CD28, the activated T cells tended to apoptosis. In order to kill tumor cells more efficiently, a recombinant multifunctional single-chain trispecific antibody (scTsAb), which contains anti-ovarian carcinoma (OC) scFv, anti-CD3 scFv and VH domain of anti-CD28 antibody, was constructed and expressed in E. coli BL21 Star strain. The scTsAb showed strong binding avidities to membrane antigen of SK-OV-3 cell, CD3 molecule on Jurkat cell, and recombinant CD28 antigen. It was further demonstrated that this scTsAb could activate peripheral blood T cells to elicit strong cytotoxicity against SK-OV-3 cells. This new type of recombinant scFv antibody set up a new technological platform for T cells based immunotherapy against cancer, especially with the failure on MHC antigen presentation or absence of costimulating signal.
对肿瘤细胞和CD3分子均具有特异性的双特异性抗体(BsAb)被认为是通过激活细胞毒性T细胞来治疗微小残留病的有前景的免疫工具。然而,在没有共刺激分子CD28的情况下,活化的T细胞易于凋亡。为了更有效地杀伤肿瘤细胞,构建了一种重组多功能单链三特异性抗体(scTsAb),其包含抗卵巢癌(OC)单链抗体片段(scFv)、抗CD3 scFv和抗CD28抗体的可变重链(VH)结构域,并在大肠杆菌BL21 Star菌株中表达。该scTsAb对SK-OV-3细胞膜抗原、Jurkat细胞上的CD3分子以及重组CD28抗原有很强的结合亲和力。进一步证明,这种scTsAb可以激活外周血T细胞,对SK-OV-3细胞产生强烈的细胞毒性。这种新型重组scFv抗体为基于T细胞的癌症免疫治疗建立了一个新的技术平台,特别是针对主要组织相容性复合体(MHC)抗原呈递失败或缺乏共刺激信号的情况。