Recombinant gamma-interferon induces changes in expression and shedding of antigens associated with normal human melanocytes, nevus cells, and primary and metastatic melanoma cells

J Immunol. 1985 Jun;134(6):4226-30.

Abstract

Recombinant gamma-interferon (rIFN-gamma) induced or augmented the expression of HLA-DR class II antigens on melanocytes isolated from newborn foreskin, from congenital, common acquired, and dysplastic nevi, and from primary and metastatic melanoma. The stimulatory effect of rIFN-gamma on HLA-DR antigen expression was suppressed by the addition of the phorbol ester TPA or its analog PDBu to the culture medium. Whereas rIFN-gamma did not significantly alter the expression of melanoma-associated, non-class II antigens on melanoma cells, there was a marked decrease in the expression of antigens associated with nevus cells. In addition, rIFN-gamma stimulated shedding of antigens. Increased antigen shedding was most apparent for an intracytoplasmic melanoma-associated protein of 80kd, followed by the ganglioside GD2 and by an alkali labile ganglioside. The simultaneous stimulation of class II antigen expression and shedding of melanoma-associated antigens as well as suppression of nevus-associated antigen expression could play an important role in the host immune response to premalignant and malignant melanocytic lesions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, Neoplasm / analysis*
  • Cells, Cultured
  • Fluorescent Antibody Technique
  • HLA-DR Antigens
  • Histocompatibility Antigens Class II / analysis
  • Humans
  • Infant, Newborn
  • Interferon-gamma / pharmacology*
  • Kinetics
  • Melanocytes / immunology*
  • Melanoma / immunology*
  • Melanoma / secondary
  • Melanoma-Specific Antigens
  • Neoplasm Proteins / analysis*
  • Nevus / immunology*
  • Receptors, Cell Surface / analysis
  • Receptors, Nerve Growth Factor

Substances

  • Antigens, Neoplasm
  • HLA-DR Antigens
  • Histocompatibility Antigens Class II
  • Melanoma-Specific Antigens
  • Neoplasm Proteins
  • Receptors, Cell Surface
  • Receptors, Nerve Growth Factor
  • Interferon-gamma