Melief C J, Kast W M
Department of Immunohematology, University Hospital Leiden, The Netherlands.
Ciba Found Symp. 1994;187:97-104; discussion 104-12. doi: 10.1002/9780470514672.ch7.
Immunotherapy of tumours by adoptive transfer of cytotoxic T lymphocytes (CTL) is now feasible in experimental murine systems. These CTL recognize peptide sequences of defined length presented by major histocompatibility complex (MHC) class I molecules. Effective eradication of large tumour masses requires co-administration of interleukin 2. Tumour escape strategies are numerous but in various instances can be counteracted by defined measures. Initiation of CTL responses against poorly immunogenic virally induced tumours and other tumours requires novel strategies to overcome T cell inertia. We propose a strategy in which CTL are raised against target molecules of choice including differentiation antigens of restricted tissue distribution (autoantigens) or mutated/overexpressed oncogene products. The steps proposed include: (1) identification of target molecules of choice. (2) Identification in these target molecules of peptides fitting MHC allele-specific peptide motifs involved in peptide binding to MHC molecules. (3) Evaluation of actual binding of such peptides to specific MHC class I molecules. (4) In vitro CTL response induction by such peptides, presented by highly efficient antigen-presenting cells such as antigen processing-defective cells carrying empty MHC class I molecules loaded with a single peptide or dendritic cells. Both types of cells are capable of primary CTL response induction in vitro. (5) Evaluation of proper processing by the demonstration of tumour cell lysis by these CTL. (6) Adoptive transfer of tumour-specific CTL generated in vitro or vaccination with peptides. These various steps have now been taken for several viruses, virally induced tumours and other types of tumours and the first indications that this strategy is useful have been obtained.
通过细胞毒性T淋巴细胞(CTL)的过继转移对肿瘤进行免疫治疗目前在实验性小鼠系统中是可行的。这些CTL识别由主要组织相容性复合体(MHC)I类分子呈递的特定长度的肽序列。有效根除大的肿瘤块需要同时给予白细胞介素2。肿瘤逃逸策略众多,但在各种情况下可以通过特定措施加以对抗。启动针对免疫原性差的病毒诱导肿瘤和其他肿瘤的CTL反应需要新的策略来克服T细胞惰性。我们提出一种策略,即针对包括组织分布受限的分化抗原(自身抗原)或突变/过表达的癌基因产物在内的选定靶分子培养CTL。提出的步骤包括:(1)识别选定的靶分子。(2)在这些靶分子中识别适合与MHC分子结合的MHC等位基因特异性肽基序的肽。(3)评估此类肽与特定MHC I类分子的实际结合情况。(4)由高效抗原呈递细胞如携带负载单一肽的空MHC I类分子的抗原加工缺陷细胞或树突状细胞呈递此类肽来体外诱导CTL反应。这两种细胞都能够在体外诱导原发性CTL反应。(5)通过证明这些CTL对肿瘤细胞的裂解来评估适当的加工情况。(6)过继转移体外产生的肿瘤特异性CTL或用肽进行疫苗接种。目前已经针对几种病毒、病毒诱导的肿瘤和其他类型的肿瘤采取了这些不同的步骤,并已获得该策略有用的初步迹象。