Scanlan M J, Jäger D
Ludwig Institute for Cancer Research, Memorial Sloan0Kettering Cancer Center, New York 10021, USA.
Breast Cancer Res. 2001;3(2):95-8. doi: 10.1186/bcr278. Epub 2001 Jan 11.
Continued progress in the development of antigen-specific breast cancer vaccines depends on the identification of appropriate target antigens, the establishment of effective immunization strategies, and the ability to circumvent immune escape mechanisms. Methods such as T cell epitope cloning and serological expression cloning (SEREX) have led to the identification of a number target antigens expressed in breast cancer. Improved immunization strategies, such as using dendritic cells to present tumor-associated antigens to T lymphocytes, have been shown to induce antigen-specific T cell responses in vivo and, in some cases, objective clinical responses. An outcome of successful tumor immunity is the evolution of antigen-loss tumor variants. The development of a polyvalent breast cancer vaccine, directed against a panel of tumor-associated antigens, may counteract this form of immune escape.
抗原特异性乳腺癌疫苗研发的持续进展取决于合适靶抗原的鉴定、有效免疫策略的建立以及规避免疫逃逸机制的能力。诸如T细胞表位克隆和血清学表达克隆(SEREX)等方法已促成了多种在乳腺癌中表达的靶抗原的鉴定。改进的免疫策略,如利用树突状细胞将肿瘤相关抗原呈递给T淋巴细胞,已显示可在体内诱导抗原特异性T细胞应答,并且在某些情况下可带来客观的临床应答。成功的肿瘤免疫的一个结果是抗原缺失肿瘤变体的演变。针对一组肿瘤相关抗原的多价乳腺癌疫苗的研发可能会对抗这种免疫逃逸形式。