Ostrand-Rosenberg S, Schwartzman M L, Hecht T T, Marr L
Cell Immunol. 1986 May;99(2):453-60. doi: 10.1016/0008-8749(86)90253-4.
The 402AX murine teratocarcinoma is a spontaneous testicular tumor of 129 (H-2b) origin which does not express MHC encoded antigens. Rejection of this tumor is immunologically mediated and the tumor cells are induced in vivo to synthesize H-2b antigens when passaged in genetically resistant host mice. The present studies demonstrate that serum from tumor primed genetically resistant host mice can induce tumor cell MHC antigen expression in vitro as measured by indirect immunofluorescence using monoclonal antibodies. The inducing factor is specific for 402AX tumor cells and is not interferon as shown by the lack of response of the 402AX tumor to gamma interferon, and the absence of significant interferon activity in inducer serum. These studies demonstrate another factor independent of interferon that can induce MHC class I antigen expression on tumor cells.
402AX小鼠畸胎癌是一种起源于129(H-2b)的自发性睾丸肿瘤,不表达MHC编码的抗原。对该肿瘤的排斥是由免疫介导的,当在基因抗性宿主小鼠中传代时,肿瘤细胞在体内被诱导合成H-2b抗原。目前的研究表明,用单克隆抗体通过间接免疫荧光法测定,来自经肿瘤致敏的基因抗性宿主小鼠的血清可在体外诱导肿瘤细胞MHC抗原表达。诱导因子对402AX肿瘤细胞具有特异性,不是干扰素,这表现为402AX肿瘤对γ干扰素无反应,且诱导血清中无显著的干扰素活性。这些研究证明了另一种独立于干扰素的因子,它可诱导肿瘤细胞上MHC I类抗原的表达。