Scholl Susy M., Michaelis Silke, McDermott Ray
J Biomed Biotechnol. 2003;2003(1):35-47. doi: 10.1155/S1110724303209037.
Over the past ten years significant advances have been made in the fields of gene therapy and tumour immunology, such that there now exists a considerable body of evidence validating the proof in the principle of gene therapy based cancer vaccines. While clinical benefit has so far been marginal, data from preclinical and early clinical trials of gene therapy combined with standard therapies are strongly suggestive of additional benefit. Many reasons have been proposed to explain the paucity of clinical responses to single agent vaccination strategies including the poor antigenicity of tumour cells and the development of tolerance through down-regulation of MHC, costimulatory, signal transduction, and other molecules essential for the generation of strong immune responses. In addition, there is now evidence from animal models that the growing tumour may actively inhibit the host immune response. Removal of the primary tumour prior to T cell transfer from the spleen of cancer bearing animals, led to effective tumour cell line specific immunity in the recipient mouse suggesting that there is an ongoing tumour-host interaction. This model also illustrates the potential difficulties of clinical vaccine trials in patients with advanced stage disease.
在过去十年里,基因治疗和肿瘤免疫学领域取得了重大进展,以至于现在有大量证据证实了基于基因治疗的癌症疫苗原理的可行性。虽然迄今为止临床获益甚微,但基因治疗与标准疗法相结合的临床前和早期临床试验数据强烈表明可能会有额外益处。人们提出了许多理由来解释单药疫苗接种策略临床反应稀少的现象,包括肿瘤细胞抗原性差以及通过下调MHC、共刺激、信号转导和其他对产生强烈免疫反应至关重要的分子而产生耐受性。此外,现在有来自动物模型的证据表明,不断生长的肿瘤可能会积极抑制宿主免疫反应。在从荷瘤动物脾脏进行T细胞转移之前切除原发性肿瘤,可在受体小鼠中产生有效的肿瘤细胞系特异性免疫,这表明存在持续的肿瘤-宿主相互作用。该模型还说明了晚期疾病患者进行临床疫苗试验可能面临的潜在困难。