Thomas Sharyn, Hart Daniel P, Xue Shao-An, Cesco-Gaspere Michela, Stauss Hans J
Expert Opin Biol Ther. 2007 Aug;7(8):1207-18. doi: 10.1517/14712598.7.8.1207.
In the last decade research has begun into the use of T-cell receptor (TCR) gene therapy as a means to control and eradicate malignancies. There is now a large body of evidence to demonstrate that through the use of this technology one can redirect T-cell antigen specificity to produce both cytotoxic and helper T cells, which are functionally competent both in vitro and in vivo and show promising antitumour effects in humans. This review focuses on the means by which TCR gene transfer is achieved and the recent advances to modify the TCRs and vector delivery systems which aim to enhance the efficiency and safety of TCR gene transfer protocols.
在过去十年中,已经开始研究使用T细胞受体(TCR)基因疗法来控制和根除恶性肿瘤。现在有大量证据表明,通过使用这项技术,可以重新定向T细胞抗原特异性,以产生细胞毒性T细胞和辅助性T细胞,这些细胞在体外和体内均具有功能活性,并在人类中显示出有前景的抗肿瘤作用。本综述重点关注实现TCR基因转移的方法,以及旨在提高TCR基因转移方案效率和安全性的TCR修饰和载体递送系统的最新进展。