Schirrmacher V
Arzneimittelforschung. 1987 Feb;37(2A):259-62.
Several approaches to increase tumor cell immunogenicity and anti-tumor T-cell reactivity have been reviewed. In contrast to unspecific immune stimulation, the activation of specific T-cell reactivity can lead to long-lasting anti-tumor immunity. In several instances, immunization with modified tumor cells led to the induction of tumor immunity against the original non-modified tumor cells. In our own studies two types of approaches were also effective with the highly metastatic mouse tumor line ESb which carries a weak tumor associated antigen. Postoperative immunization with either virus modified ESb cells or with mutagenized variants of ESb cells led to the survival of a significant proportion of the treated animals. These animals had been cured of their micrometastases and developed long lasting anti-tumor immunity. It is hoped that such modified tumor cells could become useful reagents for tumor immunotherapy, especially in situations where the tumor burden is low. Future efforts should be directed towards testing the effectiveness of immunogenic modified tumor variants in combination with surgery or chemotherapy for treatment of micrometatases.
本文综述了几种增强肿瘤细胞免疫原性和抗肿瘤T细胞反应性的方法。与非特异性免疫刺激不同,特异性T细胞反应的激活可导致持久的抗肿瘤免疫。在一些情况下,用修饰的肿瘤细胞进行免疫可诱导针对原始未修饰肿瘤细胞的肿瘤免疫。在我们自己的研究中,两种方法对携带弱肿瘤相关抗原的高转移性小鼠肿瘤细胞系ESb也有效。用病毒修饰的ESb细胞或ESb细胞的诱变变体进行术后免疫,可使相当一部分接受治疗的动物存活。这些动物的微转移灶已被治愈,并产生了持久的抗肿瘤免疫。希望这种修饰的肿瘤细胞能成为肿瘤免疫治疗的有用试剂,特别是在肿瘤负荷较低的情况下。未来的工作应致力于测试免疫原性修饰肿瘤变体与手术或化疗联合治疗微转移灶的有效性。