Er. Richards et al., ANTIBODIES REACTIVE WITH THE PROTEIN CORE OF MUC1 MUCIN ARE PRESENT IN OVARIAN-CANCER PATIENTS AND HEALTHY WOMEN, Cancer immunology and immunotherapy, 46(5), 1998, pp. 245-252
Antibodies reactive with peptide epitopes on the core protein of MUC1
epithelial mucin have been demonstrated in some patients with adenocar
cinomas. 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 patie
nts with benign and malignant ovarian tumours. Antibodies were measure
d in an enzyme-linked immunosorbent assay utilising a synthetic peptid
e 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 dec
lined progressively with age (P = 0.0006) concomitantly with increasin
g serum MUC1 levels (P = 0.003). Regardless of age, antibody levels we
re 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 cance
r (P = 0.015), multivariate regression analysis showed that this was n
ot a significant independent prognostic indicator after consideration
of the International Federation of Gynaecology and Obstetrics (FIGO) s
tage, histological type, serum MUC1 levels and age. Serial measurement
of MUC1 and MUC1 antibodies during treatment in 18 patients with ovar
ian cancer and throughout pregnancy in 10 women showed a negative corr
elation between alterations in MUC1 and MUC1 antibodies. These results
show that MUC1-peptide-reactive antibodies are present in the serum o
f healthy women and women with cancer and that they probably form immu
ne complexes with MUC1, but provide no evidence for an augmentation of
the humoral immune response to MUC1 in ovarian cancer.