Restifo N P, Minev B R, Taggarse A S, McFarland B J, Wang M, Irvine K R
Surgery Branch, Division of Cancer Treatment, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Folia Biol (Praha). 1994;40(1-2):74-88.
Activated CD8+ T cells (TCD8+) can directly recognize malignant cells because processed fragments of tumour associated antigens (TAA), 8-10 amino acids in length and complexed with MHC class I molecules, are displayed on tumour cell surfaces. Tumour cells have been genetically modified in a variety of ways in efforts to enhance the immune recognition of TAA. An alternative strategy is the expression of TAA in recombinant or synthetic form. This has been made possible by the recent cloning of TAA recognized by TCD8+. In this communication we review recent work in our own laboratory on the expression of TAA as synthetic peptide, by "naked" plasmid DNA injected intramuscularly or transdermally, and by recombinant viruses including vaccinia (rVV), fowlpox (rFV) and adenovirus (rAd). The expression of TAA in recombinant and synthetic forms allows increased control over the quantity, location, and kinetics of TAA presentation and can result in powerful, specific, anti-tumour immune responses.
活化的CD8 + T细胞(TCD8 +)能够直接识别恶性细胞,因为长度为8 - 10个氨基酸且与MHC I类分子结合的肿瘤相关抗原(TAA)的加工片段会呈现在肿瘤细胞表面。为了增强对TAA的免疫识别,肿瘤细胞已通过多种方式进行了基因改造。另一种策略是以重组或合成形式表达TAA。最近克隆出TCD8 +识别的TAA使得这成为可能。在本通讯中,我们综述了我们实验室近期关于TAA表达的研究工作,其表达形式包括合成肽、通过肌肉注射或经皮注射“裸”质粒DNA以及通过重组病毒(包括痘苗病毒(rVV)、禽痘病毒(rFV)和腺病毒(rAd))。以重组和合成形式表达TAA能够增强对TAA呈递的数量、位置和动力学的控制,并可引发强大、特异的抗肿瘤免疫反应。