Hölsken Oliver, Miller Matthias, Cerwenka Adelheid
Innate Immunity Group (D080), German Cancer Research Center (DKFZ), Heidelberg, Germany.
J Dtsch Dermatol Ges. 2015 Jan;13(1):23-9. doi: 10.1111/ddg.12557.
During the recent years, immunotherapy has obtained substantial impact on the clinical treatment of melanoma. Besides promising approaches based on T lymphocytes, natural killer (NK) cells have gained more and more attention as anti-melanoma effector cells. NK cell activation is inhibited by HLA class I molecules expressed by target cells, so they preferentially attack tumor cells that express low levels of HLA class I. Partial or complete loss of HLA class I expression is a frequent event during the development of melanoma. In parallel, ligands for activating NK cell receptors become induced upon malignant transformation. Thus, melanoma cells are often efficiently recognized and lysed by NK cells at least in vitro. In vivo, however, melanomas have developed multiple sophisticated strategies to escape from NK cell mediated attack. Several novel approaches aim at harnessing NK cells to treat melanoma patients and to counteract existing tumor escape mechanisms. This review summarizes the most recent advances in the field.
近年来,免疫疗法对黑色素瘤的临床治疗产生了重大影响。除了基于T淋巴细胞的有前景的方法外,自然杀伤(NK)细胞作为抗黑色素瘤效应细胞越来越受到关注。NK细胞的激活受到靶细胞表达的HLA I类分子的抑制,因此它们优先攻击HLA I类表达水平低的肿瘤细胞。HLA I类表达的部分或完全丧失是黑色素瘤发生过程中的常见事件。同时,激活NK细胞受体的配体在恶性转化时被诱导。因此,黑色素瘤细胞通常至少在体外能被NK细胞有效识别并裂解。然而,在体内,黑色素瘤已经发展出多种复杂的策略来逃避NK细胞介导的攻击。几种新方法旨在利用NK细胞治疗黑色素瘤患者并对抗现有的肿瘤逃逸机制。本综述总结了该领域的最新进展。