Richards E R, Devine P L, Quin R J, Fontenot J D, Ward B G, McGuckin M A
Department of Obstetrics and Gynaecology, University of Queensland, Royal Brisbane Hospital, Herston, Australia.
Cancer Immunol Immunother. 1998 Jul;46(5):245-52. doi: 10.1007/s002620050484.
Antibodies reactive with peptide epitopes on the core protein of MUC1 epithelial mucin have been demonstrated in some patients with adenocarcinomas. Because these epitopes can be exposed on MUC1 in the serum of healthy women, we measured concentrations of MUC1-reactive antibodies in the serum of healthy pregnant and non-pregnant women, and in patients with benign and malignant ovarian tumours. Antibodies were measured in an enzyme-linked immunosorbent assay utilising a synthetic peptide corresponding to a 105-amino-acid segment of the MUC1 tandem repeat region (5.25 repeats). MUC1-reactive antibodies were always of an IgM isotype and concentrations were highest in young healthy women and declined progressively with age (P=0.0006) concomitantly with increasing serum MUC1 levels (P=0.003). Regardless of age, antibody levels were lower in cancer patients than in healthy women (P<0.0001), but MUC1 levels were much higher in cancer patients (P<0.0001). Although high antibody levels were associated with greater survival in ovarian cancer (P=0.015), multivariate regression analysis showed that this was not a significant independent prognostic indicator after consideration of the International Federation of Gynaecology and Obstetrics (FIGO) stage, histological type, serum MUC1 levels and age. Serial measurement of MUC1 and MUC1 antibodies during treatment in 18 patients with ovarian cancer and throughout pregnancy in 10 women showed a negative correlation between alterations in MUC1 and MUC1 antibodies. These results show that MUC1-peptide-reactive antibodies are present in the serum of healthy women and women with cancer and that they probably form immune complexes with MUC1, but provide no evidence for an augmentation of the humoral immune response to MUC1 in ovarian cancer
在一些腺癌患者中已证实存在与MUC1上皮粘蛋白核心蛋白上的肽表位发生反应的抗体。由于这些表位在健康女性血清中的MUC1上可能会暴露,我们检测了健康孕妇和非孕妇以及患有良性和恶性卵巢肿瘤患者血清中与MUC1反应的抗体浓度。在酶联免疫吸附测定中,使用与MUC1串联重复区域的105个氨基酸片段(5.25个重复)相对应的合成肽来检测抗体。与MUC1反应的抗体始终为IgM同种型,浓度在年轻健康女性中最高,并随着年龄的增长而逐渐下降(P = 0.0006),同时血清MUC1水平升高(P = 0.003)。无论年龄如何,癌症患者的抗体水平均低于健康女性(P <0.0001),但癌症患者的MUC1水平要高得多(P <0.0001)。尽管高抗体水平与卵巢癌患者的生存期延长相关(P = 0.015),但多因素回归分析表明,在考虑国际妇产科联合会(FIGO)分期、组织学类型、血清MUC1水平和年龄后,这并不是一个显著的独立预后指标。对18例卵巢癌患者治疗期间以及10例女性整个孕期的MUC1和MUC1抗体进行连续测量,结果显示MUC1和MUC1抗体的变化呈负相关。这些结果表明,与MUC1肽反应的抗体存在于健康女性和癌症女性的血清中,它们可能与MUC1形成免疫复合物,但没有证据表明卵巢癌患者对MUC1的体液免疫反应增强。