Schultze J L, Gribben J G, Nadler L M
Department of Adult Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Curr Opin Oncol. 1998 Nov;10(6):542-7. doi: 10.1097/00001622-199811000-00011.
It is now widely accepted that current standard therapy does not lead to cure for the majority of patients with B-cell malignancies. In the search for novel treatment modalities and with the discovery of tumor-antigen--derived peptides recognized by T cells in the context of major histocompatibility complex class I and II molecules, active and passive immunotherapy has moved to center stage once again. Whereas most lymphoma research in this area has focused on vaccination strategies using the tumor-specific idiotype as a target antigen, this review focuses on the potential of a new strategy of adoptive transfer of antigen-specific T- for B-cell malignancies. Murine in vivo models and preclinical experiments suggest that we are now ready to enter the clinical arena to evaluate whether adoptive transfer of autologous or allogeneic antigen-specific T cells is a feasible and efficacious therapy approach for the treatment of B-cell malignancies. Potential obstacles to this strategy are also discussed.
目前已广泛接受的观点是,当前的标准疗法无法治愈大多数B细胞恶性肿瘤患者。在寻找新的治疗方式以及发现主要组织相容性复合体I类和II类分子背景下被T细胞识别的肿瘤抗原衍生肽后,主动和被动免疫疗法再次成为焦点。尽管该领域的大多数淋巴瘤研究都集中在以肿瘤特异性独特型作为靶抗原的疫苗接种策略上,但本综述重点关注抗原特异性T细胞过继转移治疗B细胞恶性肿瘤这一新策略的潜力。小鼠体内模型和临床前实验表明,我们现在已准备好进入临床领域,以评估自体或异体抗原特异性T细胞的过继转移是否是治疗B细胞恶性肿瘤的一种可行且有效的治疗方法。同时也讨论了该策略的潜在障碍。