Does pregnancy immunize against breast cancer?

Cancer Res. 1995 Jun 1;55(11):2257-61.

Abstract

Multiparity has been linked with protection against breast cancer. T cells from biparous women, but not T cells from nulliparous women or men, 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 pregnancy, and their T cells proliferated specifically in response to MUC-1 mucin. These observations support the hypothesis that there is a natural immunization against MUC-1 peptide epitopes during pregnancy which provides some protection against the development of breast cancer. These data also suggest that certain MUC-1 synthetic peptides might be effective components of "vaccines" for therapy or prevention of breast cancer.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Breast Neoplasms / immunology*
  • Breast Neoplasms / prevention & control*
  • CD4-Positive T-Lymphocytes / cytology
  • Epitopes / immunology
  • Female
  • Humans
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / pharmacology*
  • Molecular Sequence Data
  • Mucin-1
  • Mucins / immunology
  • Mucins / pharmacology*
  • Parity
  • Peptide Fragments / pharmacology*
  • Pregnancy / blood
  • Pregnancy / immunology*
  • Sensitivity and Specificity
  • T-Lymphocyte Subsets
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology

Substances

  • Epitopes
  • Membrane Glycoproteins
  • Mucin-1
  • Mucins
  • Peptide Fragments