Andersen M H, Pedersen L O, Becker J C, Straten P T
Department of Tumor Cell Biology, Danish Cancer Society, Copenhagen.
Cancer Res. 2001 Feb 1;61(3):869-72.
During the last decade, a large number of human tumor-associated antigens have been identified that are recognized by CTLs in a MHC-restricted fashion. The apoptosis inhibitor protein survivin is overexpressed in most human cancers, and inhibition of its function results in increased apoptosis. Therefore, this protein may serve as a target for therapeutic CTL responses. Here, using CTL epitopes deduced from survivin, we describe specific T-cell reactivity against this antigen in peripheral blood from chronic lymphatic leukemia patients and in tumor-infiltrated lymph nodes from melanoma patients by ELISPOT analysis. CTL responses against two survivin-deduced peptide epitopes were detected in three of six melanoma patients and three of four chronic lymphatic leukemia patients. No T-cell reactivity was detected in peripheral blood lymphocytes from six healthy controls. Thus, survivin may serve as an important and widely applicable target for anticancer immunotherapeutic strategies.
在过去十年中,已鉴定出大量人类肿瘤相关抗原,这些抗原以MHC限制的方式被细胞毒性T淋巴细胞(CTL)识别。凋亡抑制蛋白survivin在大多数人类癌症中过度表达,抑制其功能会导致细胞凋亡增加。因此,这种蛋白可能成为治疗性CTL反应的靶点。在此,我们利用从survivin推导的CTL表位,通过ELISPOT分析描述了慢性淋巴细胞白血病患者外周血和黑色素瘤患者肿瘤浸润淋巴结中针对该抗原的特异性T细胞反应性。在六名黑色素瘤患者中的三名以及四名慢性淋巴细胞白血病患者中的三名中检测到针对两种从survivin推导的肽表位的CTL反应。在六名健康对照者的外周血淋巴细胞中未检测到T细胞反应性。因此,survivin可能成为抗癌免疫治疗策略的一个重要且广泛适用的靶点。