Turbeville M A, Rhodes J C, Hyams D M, Distler C M, Steele P E
Department of Pathology and Laboratory Medicine, University of Cincinnati College of Medicine, Ohio 45267-0529, USA.
Pathobiology. 1996;64(5):233-8. doi: 10.1159/000164053.
Tumor-induced immunosuppression by murine retrovirus-induced tumors and nonviral murine and human tumors has been shown to be mediated by the transmembrane (TM) envelope (env) protein p15E. This in vitro activity is inhibitable by anti-(murine)p15E antibodies, implying that a TM-like protein is produced by such tumors. The leading candidate genes that might encode such proteins in human tumors are human endogenous retroviral (HERV) sequences. We have utilized immunohistochemistry to determine what tissues may express HERV env proteins. We subcloned a restriction fragment from the putative TM human env gene of a type C-related HERV (clone-4-1) into a fusion protein gene construct. Using a rabbit polyclonal antiserum against the fusion protein, we observed staining in a variety of human tumor and nontumor tissues.
小鼠逆转录病毒诱导的肿瘤以及非病毒的小鼠和人类肿瘤所引发的肿瘤诱导性免疫抑制已被证明是由跨膜(TM)包膜(env)蛋白p15E介导的。这种体外活性可被抗(小鼠)p15E抗体抑制,这意味着此类肿瘤会产生一种类似TM的蛋白。在人类肿瘤中可能编码此类蛋白的首要候选基因是人类内源性逆转录病毒(HERV)序列。我们利用免疫组织化学来确定哪些组织可能表达HERV env蛋白。我们从一种C型相关HERV(克隆-4-1)的假定TM人类env基因中克隆了一个限制性片段,将其插入到一个融合蛋白基因构建体中。使用针对该融合蛋白的兔多克隆抗血清,我们在多种人类肿瘤和非肿瘤组织中观察到了染色。