Chigira M, Shinozaki T, Watanabe H
Oncol Rep. 1995 May;2(3):397-415. doi: 10.3892/or.2.3.397.
The close correlation found between malignancies and autoimmune disorders suggests that a common pathogenetic mechanism plays a role in both disorders. Recent results obtained by analysis of V-H and V-L genes of autoreactive immunocytes reveal their oligo-clonality. They are essentially autoreactive with developmental antigens since these clones are prepared to recognize normal antigens without somatic mutations. Under the concept that immunity recognize developmental antigens as well as foreign antigens, it is conceivable that auto-reactivity is induced by an autonomy of immunocytes, when antigenic duality between self and non-self is an essential feature of immunity. In this process, autoimmunity due to malignancy is non-teleologic, since autoimmunity programmed a priori within immunocytes is expressed in an autonomic manner caused by cellular selfishness. On the other hand, paraneoplastic autoimmunity with non-immunocyte tumors suggests a mechanism differing from autonomic expansion of immunocytes. In order to explain this phenomenon, there are two possibilities: the first is that tumor cells secrete immune molecules including immunoglobulins and the second is that so-called antigen drive is related with curious MHC expression of tumor cells, with or without molecular mimicry due to somatic mutations. Both mechanisms are essentially non-teleological.
恶性肿瘤与自身免疫性疾病之间存在的密切关联表明,一种共同的发病机制在这两种疾病中均发挥作用。近期通过对自身反应性免疫细胞的V-H和V-L基因进行分析所获得的结果揭示了它们的寡克隆性。它们主要对发育抗原具有自身反应性,因为这些克隆已准备好识别正常抗原而无需体细胞突变。在免疫可识别发育抗原以及外来抗原这一概念下,可以想象,当自身与非自身之间的抗原二元性是免疫的一个基本特征时,免疫细胞的自主性会诱导自身反应性。在这个过程中,由恶性肿瘤导致的自身免疫是无目的性的,因为预先在免疫细胞中编程的自身免疫是以由细胞自私性引起的自主方式表达的。另一方面,非免疫细胞肿瘤伴发的副肿瘤性自身免疫提示了一种不同于免疫细胞自主扩增的机制。为了解释这一现象,存在两种可能性:第一种是肿瘤细胞分泌包括免疫球蛋白在内的免疫分子,第二种是所谓的抗原驱动与肿瘤细胞奇特的MHC表达有关,无论是否存在由于体细胞突变导致的分子模拟。这两种机制本质上都是无目的性的。