Robbins P F, Kawakami Y
Surgery Branch, National Institutes of Health, National Cancer Institute, Bethesda, MD 20892-1502, USA.
Curr Opin Immunol. 1996 Oct;8(5):628-36. doi: 10.1016/s0952-7915(96)80078-1.
The ability of tumor-reactive T cells to mediate in vivo tumor regression has been demonstrated in murine tumor models and by the clinical responses to adoptive immunotherapy with tumor-infiltrating lymphocytes isolated from human melanomas. Investigations carried out in the past several years have resulted in the isolation of a number of the genes encoding antigens recognized by melanoma-reactive T cells. The ability of these products to serve as tumor regression antigens has now begun to be evaluated in clinical vaccine trials.
肿瘤反应性T细胞介导体内肿瘤消退的能力已在小鼠肿瘤模型中得到证实,并且通过对从人类黑色素瘤中分离出的肿瘤浸润淋巴细胞进行过继性免疫治疗后的临床反应也得到了证实。过去几年开展的研究已分离出许多编码黑色素瘤反应性T细胞所识别抗原的基因。这些产物作为肿瘤消退抗原的能力现已开始在临床疫苗试验中进行评估。