Multiparity has been linked with protection against breast cancer, T c
ells from biparous women, but not T cells from nulliparous women or me
n, specifically proliferated in response to core peptide sequences of
a human breast cancer-associated mucin (MUC-1), Two of the nulliparous
women were retested during the first trimester of their first pregnan
cy, and their T cells proliferated specifically in response to MUC-1 m
ucin, These observations support the hypothesis that there is a natura
l immunization against MUC-1 peptide epitopes during pregnancy which p
rovides some protection against the development of breast cancer, Thes
e data also suggest that certain MUC-1 synthetic peptides might be eff
ective components of ''vaccines'' for therapy or prevention of breast
cancer.