Dummer R, Davis-Daneshfar A, Döhring C, Döbbeling U, Burg G
Dermatologische Klinik, Universitätsspital, Zürich.
Hautarzt. 1995 May;46(5):305-8. doi: 10.1007/s001050050256.
Active unspecific immunotherapy in an adjuvant or palliative setting has been shown to enhance survival in melanoma patients, and gene therapy now offers new perspectives for active specific immunotherapy. Gene therapy includes the transfer of genetic material performed by either viral or non-viral methods and in vivo or ex vivo. For melanoma the following approaches are suggested: vaccination with tumour-specific, HLA-associated antigens using peptides or 'naked DNA', vaccination with melanoma cells transfected with cytokine genes or B7, adoptive immunotherapy with specific T-lymphocytes or transfected tumour-infiltrating lymphocytes, or transfection of tumour cells with a tumour suppressor gene whose dysfunction plays a crucial role in melanoma.
在辅助或姑息治疗中,主动非特异性免疫疗法已被证明可提高黑色素瘤患者的生存率,而基因治疗如今为主动特异性免疫疗法提供了新的前景。基因治疗包括通过病毒或非病毒方法以及体内或体外进行遗传物质的转移。对于黑色素瘤,建议采用以下方法:使用肽或“裸DNA”接种肿瘤特异性、HLA相关抗原,接种用细胞因子基因或B7转染的黑色素瘤细胞,用特异性T淋巴细胞或转染的肿瘤浸润淋巴细胞进行过继性免疫治疗,或用一种肿瘤抑制基因转染肿瘤细胞,该基因功能障碍在黑色素瘤中起关键作用。