Boyer C M, Dawson D V, Neal S E, Winchell L F, Leslie D S, Ring D, Bast R C
Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.
Cancer Res. 1989 Jun 1;49(11):2928-34.
Treatment of cancer cells with interferons can modulate expression of cell surface antigens, particularly those of the major histocompatibility complex (MHC). To examine the effect of recombinant gamma- and alpha-interferons on expression of non-MHC antigens, murine monoclonal antibodies have been used to quantitate 14 distinct tumor-associated cell surface antigens from five breast cancer cell lines and five ovarian cancer cell lines using a live cell radioimmunoassay. Both Class I and Class II MHC antigens could be augmented or induced with gamma-interferon. Significantly increased expression of MHC antigens was observed in nine of 10 cell lines with induction indices as high as 11-fold. When 17 non-MHC epitopes were measured on 10 cell lines, minimal (1.3-2.7-fold) induction was observed in 10 of the 170 instances evaluated. Expression of only two epitopes, 2G3 and 735B11, was increased on more than one cell line. On six cell lines expression of non-MHC epitopes could not be increased. Consequently, among many different cell surface determinants, interferons produced a highly selective augmentation or induction of MHC antigens, whereas augmentation or induction of other tumor-associated antigens was apparently restricted to a few epitopes.
用干扰素处理癌细胞可调节细胞表面抗原的表达,尤其是主要组织相容性复合体(MHC)的抗原。为了研究重组γ干扰素和α干扰素对非MHC抗原表达的影响,已使用鼠单克隆抗体通过活细胞放射免疫测定法定量来自五个乳腺癌细胞系和五个卵巢癌细胞系的14种不同的肿瘤相关细胞表面抗原。I类和II类MHC抗原均可被γ干扰素增强或诱导。在10个细胞系中的9个中观察到MHC抗原的表达显著增加,诱导指数高达11倍。当在10个细胞系上测量17个非MHC表位时,在评估的170个实例中的10个中观察到最小(1.3 - 2.7倍)的诱导。仅在一个以上的细胞系上观察到2G3和735B11这两个表位的表达增加。在六个细胞系上,非MHC表位的表达无法增加。因此,在许多不同的细胞表面决定簇中,干扰素对MHC抗原产生高度选择性的增强或诱导作用,而其他肿瘤相关抗原的增强或诱导显然仅限于少数表位。