Suppr超能文献

一种产生针对肿瘤细胞细胞毒性的新型三特异性抗体模型。

A new model of trispecific antibody resulting the cytotoxicity directed against tumor cells.

作者信息

Song Li-Ping, Cheng Ju-Long, Wang Xiang-Bin, Zhang Zhong, Fang Min, Zhou Zhi-Yong, Huang Hua-Liang

机构信息

Institute of Genetics and Developmental Biology, the Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003 Jun;35(6):503-10.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验