Chang Chien-Chung, Ferrone Soldano
Department of Structural Biology, Hauptman-Woodward Medical Research Institute, Buffalo, NY 14203, USA.
Semin Cancer Biol. 2006 Oct;16(5):383-92. doi: 10.1016/j.semcancer.2006.07.001. Epub 2006 Jul 7.
Malignant transformation of cells is frequently associated with HLA class I antigen downregulation or loss. This abnormality provides malignant cells with a mechanism to escape control by HLA class I antigen-restricted, tumor antigen-specific cytotoxic T lymphocytes. Surprisingly, HLA class I antigen downregulation or loss by tumor cells is not associated with control of tumor growth by natural killer (NK) cells, as it would be predicted by the "missing-self" hypothesis. Here, we discuss the role of NK cell activating ligand abnormalities as well as HLA class I molecule and ICAM-1 shedding in the lack of control of tumor growth by NK cells with emphasis on their molecular mechanisms. In addition, we discuss the impact of these abnormalities on cancer immune surveillance.
细胞的恶性转化常常与HLA I类抗原下调或缺失相关。这种异常为恶性细胞提供了一种机制,使其能够逃避受HLA I类抗原限制的、肿瘤抗原特异性细胞毒性T淋巴细胞的控制。令人惊讶的是,肿瘤细胞的HLA I类抗原下调或缺失与自然杀伤(NK)细胞对肿瘤生长的控制无关,而“缺失自我”假说本应预测二者有关。在此,我们讨论NK细胞激活配体异常以及HLA I类分子和细胞间黏附分子-1(ICAM-1)脱落在NK细胞无法控制肿瘤生长中的作用,并重点阐述其分子机制。此外,我们还讨论了这些异常对癌症免疫监视的影响。