Maudsley D J, Bateman W J, Morris A G
Department of Biological Sciences, University of Warwick, Coventry, U.K.
Immunology. 1991 Feb;72(2):277-81.
A number of viral genes and cellular oncogenes inhibit major histocompatibility complex (MHC) antigen expression at the cell surface. In the case of inhibition of class I MHC antigens by viral genes this results in a reduced recognition by antigen-specific cytotoxic T cells. The activated Ki-ras cellular oncogene carried by the Ki-murine sarcoma virus (Ki-MuSV) in contrast inhibits class II MHC (or Ia) antigen expression on transformed cells. We have studied how transformation with Ki-ras affects recognition by alloreactive helper T cells. We found that the Ki-ras inhibition of class II MHC antigen expression led to greatly reduced stimulation of alloreactive T cells to proliferate and to secrete interferon-gamma (IFN-gamma). These findings support our hypothesis that the ability of an oncogene to reduce class II MHC antigen expression is crucial to its ability to produce tumour cells.
许多病毒基因和细胞癌基因会抑制细胞表面主要组织相容性复合体(MHC)抗原的表达。就病毒基因对I类MHC抗原的抑制而言,这会导致抗原特异性细胞毒性T细胞的识别减少。相比之下,Ki-小鼠肉瘤病毒(Ki-MuSV)携带的活化型Ki-ras细胞癌基因会抑制转化细胞上的II类MHC(或Ia)抗原表达。我们研究了用Ki-ras进行转化如何影响同种反应性辅助性T细胞的识别。我们发现,Ki-ras对II类MHC抗原表达的抑制导致同种反应性T细胞增殖和分泌γ干扰素(IFN-γ)的刺激大大减少。这些发现支持了我们的假设,即癌基因降低II类MHC抗原表达的能力对其产生肿瘤细胞的能力至关重要。