James R F, Edwards S, Hui K M, Bassett P D, Grosveld F
Department of Surgery, Leicester University, U.K.
Immunology. 1991 Feb;72(2):213-8.
There is much evidence to suggest that potentially immunogenic tumour cells can escape cytolytic immune destruction by loss of class I antigen expression. Many tumours are allele-specific class I negative and, in murine systems, reconstitution of class I expression by gene transfection leads to an increase in tumour immunogenicity. In many systems where mice have rejected class I transfected tumour cells they are also immune to a subsequent challenge with the untransfected parent tumour. In this study we have examined the effect of stable class II antigen expression (induced by gene transfection) on a class I loss mutant (H-2Kk negative) murine cell line, K36.16. We show that H-2Ek expression is more effective at increasing tumour immunogenicity than the reconstitution of H-2Kk expression in these cells. This suggests that the induction of class II antigen expression on tumour cells may provide an effective way of enhancing tumour-specific immune responses in vivo.
有许多证据表明,具有潜在免疫原性的肿瘤细胞可通过丧失I类抗原表达来逃避溶细胞性免疫破坏。许多肿瘤是等位基因特异性I类阴性,在鼠类系统中,通过基因转染重建I类表达会导致肿瘤免疫原性增加。在许多小鼠排斥I类转染肿瘤细胞的系统中,它们对随后未转染的亲本肿瘤攻击也具有免疫力。在本研究中,我们检测了稳定的II类抗原表达(由基因转染诱导)对I类缺失突变体(H-2Kk阴性)鼠细胞系K36.16的影响。我们发现,在这些细胞中,H-2Ek表达在增加肿瘤免疫原性方面比重建H-2Kk表达更有效。这表明在肿瘤细胞上诱导II类抗原表达可能是在体内增强肿瘤特异性免疫反应的一种有效方法。