Klein G, Klein E
Transplant Proc. 1977 Mar;9(1):1095-104.
In contrast to the excellent surveillance against tumors induced by the ubiquitous viruses in their natural host species, spontaneous tumors developing naturally, without experimental interference, evoke little or no rejection reaction. This may be viewed in relation to the natural history of tumors. In most cases, tumors evolve in several steps, with a successful of clonal variants following each other, characterized by increasing independence of host regulations (including immune restrictions). This process is commonly designated as tumor progression. In all probability, selection for nonrejectability is part of this process. Selection of the host for rejecting capacity is unlikely to play any major role, since the overwhelming majority of the naturally occurring tumors arise after the host has passed the peak of its reproductive period. The nonrejectability of spontaneous tumors may be overcome by target-cell modification, e.g., by chemical coupling, somatic cell hybridization, or viral xenogenization. Furthermore, genetic analysis of the F1 resistance effect in relation to seemingly nonrejectable tumors may reveal the existence of specific immune-response (Ir) genes that can influence the recognition of tumor-associated membrane changes by the host immune system.
与对其自然宿主物种中普遍存在的病毒所诱导肿瘤的出色监测形成对比的是,在没有实验干预的情况下自然发生的自发性肿瘤几乎不会引发或根本不会引发排斥反应。这可以从肿瘤的自然史角度来审视。在大多数情况下,肿瘤会经历几个阶段的演变,相继出现一系列成功的克隆变体,其特征是对宿主调控(包括免疫限制)的依赖性不断增加。这个过程通常被称为肿瘤进展。很有可能,选择不可排斥性是这个过程的一部分。选择具有排斥能力的宿主不太可能发挥任何主要作用,因为绝大多数自然发生的肿瘤是在宿主度过其生殖期高峰之后出现的。自发性肿瘤的不可排斥性可以通过对靶细胞进行修饰来克服,例如通过化学偶联、体细胞杂交或病毒异种移植。此外,对与看似不可排斥的肿瘤相关的F1抗性效应进行遗传分析,可能会揭示特定免疫反应(Ir)基因的存在,这些基因能够影响宿主免疫系统对肿瘤相关膜变化的识别。