Isolation of MUC1-primed B lymphocytes from tumour-draining lymph nodes by immunomagnetic beads

Cancer Immunol Immunother. 1999 Jan;47(5):272-7. doi: 10.1007/s002620050531.

Abstract

The humoral immune response against a tumour-associated antigen, polymorphic epithelial mucin (PEM, MUC1) in cancer patients was studied by isolating specific B cells primed for the antigen. Human B lymphocytes from tumour-draining lymph nodes, obtained from 12 patients with epithelial cancers, were immunoselected with magnetic beads coated with a 60mer synthetic peptide corresponding to three tandem repeats of the protein core of the MUC1 antigen. Short-term cultures of B cells were established utilizing interleukin-10 (IL-10), IL-4 and monoclonal antibody anti-CD40, and were maintained for a maximum of 3 weeks. B cell culture supernatants contained human anti-MUC1 antibodies, as detected by enzyme-linked immunosorbent assay, in 6/12 of the patients tested. Five of these patients, all with early-stage cancer, also had high levels of circulating anti-MUC1 IgM antibodies in the serum. A significant correlation was found (two-tailed P = 0.041) between the presence of circulating anti-MUC1 antibodies and the ability to isolate PEM-specific B cells from tumour-draining lymph nodes. The technique proposed provides a useful method for the analysis of natural immunity against defined tumour antigens.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Neoplasm / blood
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / pathology
  • Breast Neoplasms / immunology
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Genital Neoplasms, Female / immunology
  • Humans
  • Immunoglobulin G / immunology
  • Immunoglobulin M / immunology
  • Immunomagnetic Separation / methods*
  • Lymph Nodes / immunology
  • Lymph Nodes / pathology*
  • Middle Aged
  • Mucins / immunology*
  • Neoplasms / immunology*
  • Neoplasms / pathology
  • Stomach Neoplasms / immunology

Substances

  • Antibodies, Neoplasm
  • Immunoglobulin G
  • Immunoglobulin M
  • Mucins