Skip to main content
Log in

Modulation by cytokines of HLA antigens, intercellular adhesion molecule 1 and high molecular weight melanoma associated antigen expression and of immune lysis of clones derived from the melanoma cell line MeM 50-10

  • Original articles
  • Published:
Cancer Immunology, Immunotherapy Aims and scope Submit manuscript

Summary

Clones were isolated from the cultured human melanoma cell line MeM 50-10, which metastasizes in nude mice with a pattern similar to that in patients with melanoma. Analysis with monoclonal antibodies detected heterogeneity among the clones in the expression of HLA class I antigens, HLA class II antigens, intercellular adhesion molecule 1 and high molecular weight melanoma associated antigen. The clones MeM A16 and MeM A18 were also shown to display differential susceptibility to modulation by immune interferon (IFN-γ) and/or tumor necrosis factor (TNF-α) of the expression of the four types of antigens analyzed. In spite of differences in the antigenic profile, the two clones did not differ in their susceptibility to lysis by lymphokine-activated killer (LAK) cells and by anti-HLA-A2 cytotoxic T cells. The increase in the expression of HLA class I antigens induced by IFN-γ and/or TNF-α on the two clones was associated with an increased susceptibility to lysis by anti-HLA-A2 cytotoxic T cells. Because of the metastasizing properties of cultured melanoma cells MeM 50-10, the clones we have isolated, with their distinct antigenic profile and differential susceptibility to modulation by cytokines, may represent useful models to investigate the role of distinct antigenic structures in the metastatic process.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Albino AP, Lloyd KO, Houghton AN, Oettgen HF, Old LJ (1981) Heterogeneity in surface antigen and glycoprotein expression of cell lines derived from different melanoma metastases of the same patient. J Exp Med 154: 1764

    Google Scholar 

  2. Anichini A, Fossati G, Parmiani G (1986) Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones. J Exp Med 163: 215

    Google Scholar 

  3. Anichini A, Mortarini R, Fossati G, Parmiani G (1986) Phenotypic profile of clones from early cultures of human metastatic melanomas and its modulation by recombinant interferon γ. Int J Cancer 38: 505

    Google Scholar 

  4. Barnstable CJ, Bodmer WF, Brown G, Galfre G, Milstein C, Williams AF, Ziegler A (1978) Production of monoclonal antibodies to group A erythrocytes, HLA and other human cell surface antigens-New tools for genetic analysis. Cell 14: 9

    Google Scholar 

  5. Bonner WM, Laskey RA (1974) A film detection method for tritium-labelled proteins and nucleic acids in polyacrylamidegels. Eur J Biochem 46: 83

    Google Scholar 

  6. Cillo C, Mach J-P, Schreyer M, Carrel S (1984) Antigenic heterogeneity of clones and subclones from human melanoma cell lines demonstrated by a panel of monoclonal antibodies and flow microfluorometry analysis. Int J Cancer 34: 11

    Google Scholar 

  7. Dougherty GJ, Murdoch S, Hogg N (1988) The function of human intercellular adhesion molecule-1 (ICAM-1) in the generation of an immune response. Eur J Immunol 18: 35

    Google Scholar 

  8. Feinberg AP, Vogelstein B (1983) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132: 6

    Google Scholar 

  9. Ferrone S, Imberti L, Natali PG, Schrier PI, Ruiter D (1986) HLA antigens on tumor cells. In: Roth JA (ed) Monoclonal antibodies in cancer: advances in diagnosis and treatment. Futura Publishing Company, New York, pp 111–139

    Google Scholar 

  10. Ferrone S, Temponi M, Gargiulo D, Scassellati GA, Cavaliere R, Natali PG (1988) Selection and utilization of monoclonal antibody defined melanoma associated antigens for immunoscintigraphy in patients with melanoma: In: Srivastava S (ed) Radiolabeled monoclonal antibodies for imaging and therapy, vol 152. Plenum Press, New York and London, p 55

    Google Scholar 

  11. Giacomini P, Veglia F, Cordiali Fei P, Rehle T, Natali PG, Ferrone S (1984) Level of a membrane-bound high-molecularweight melanoma-associated antigen and a cytoplasmic melanoma-associated antigen in surgically removed tissues and in sera from patients with melanoma. Cancer Res 44: 1281

    Google Scholar 

  12. Goldberg DA (1980) Isolation and partial characterization of theDrosophila alcohol dehydrogenase gene. Proc Natl Acad Sci USA 77: 5794

    Google Scholar 

  13. Greenwood FC, Hunter WM, Glover JS (1963) The preparation of131I-labelled human growth hormone of high specific radioactivity. Biochem J 89: 114

    Google Scholar 

  14. Herin M, Lemoine C, Weynants P, Vessiere F, Van Pel A, Knuth A, Devos R, Boon T (1987) Production of stable cytolytic T-cell clones directed against autologous human melanoma. Int J Cancer 39: 390

    Google Scholar 

  15. Houghton AN, Real FX, Davis LJ, Cordon-Cardo C, Old LJ (1987) Phenotypic heterogeneity of melanoma. Relation to the differentiation program of melanoma cells. J Exp Med 165: 812

    Google Scholar 

  16. Kerbel RS, Man MS (1984) Single-step selection of unique human melanoma variants displaying unusually aggressive metastatic behavior in nude athymic mice. Invasion Metastasis 4: 31 (suppl)

    Google Scholar 

  17. Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680

    Google Scholar 

  18. Lapierre LA, Fiers W, Pober JS (1988) Three distinct classes of regulatory cytokines control endothelial cell MHC antigen expression. Interactions with immune γ interferon differentiate the effects of tumor necrosis factor and lymphotoxin from those of leukocyte α and fibroblast β interferons. J Exp Med 167: 794

    Google Scholar 

  19. Leeuwenberg JFM, Van Damme J, Meager T, Jeunhomme TMAA, Buurman WA (1988) Effects of tumor necrosis factor in the interferon-γ-induced major histocompatibility complex class II antigens expression by human endothelial cells. Eur J Immunol 18: 1469

    Google Scholar 

  20. Maio M, Gulwani B, Tombesi S, Langer JA, Duigou GJ, Kerbel RS, Fisher PB, Ferrone S (1988) Differential induction by immune interferon of the gene products of the HLA-D region on the melanoma cell line MeWo and its metastatic variant MeM 50-10. J Immunol 141: 913

    Google Scholar 

  21. Maio M, Gulwani B, Langer JA, Kerbel RS, Duigou GJ, Fisher PB, Ferrone S (1989) Modulation by interferons of HLA antigen, and intercellular adhesion molecule 1 expression by cultured melanoma cells with different metastatic potential. Cancer Res 49: 2980

    Google Scholar 

  22. Maio M, Gulwani B, Morgano A, Ferrone S Differential modulation by tumor necrosis factor and immune interferon of HLA Class II antigens expressed by melanoma cells. Int J Cancer, in press

  23. Makgoba MW, Sanders ME, Ginther Luce GE, Gugel EA, Dustin ML, Springer TA, Shaw S (1988) Functional evidence that intercellular adhesion molecule-1 (ICAM-1) is a ligand for LFA-1-dependent adhesion in T cell-mediated cytotoxicity. Eur J Immunol 18: 637

    Google Scholar 

  24. Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning. A laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY

    Google Scholar 

  25. Matsui M, Temponi M, Ferrone S (1987) Characterization of a monoclonal antibody-defined human melanoma-associated antigen susceptible to induction by immune interferon. J Immunol 139: 2088

    Google Scholar 

  26. Natali PG, Cavaliere R, Bigotti A, Nicotra MR, Russo C, Ng A-K, Giacomini P, Ferrone S (1983) Antigenic heterogeneity of surgically removed primary and autologous metastatic human melanoma lesions. J Immunol 130: 1462

    Google Scholar 

  27. Natali PG, Bigotti A, Cavaliere R, Nicotra MR, Ferrone S (1984) Phenotyping of lesions of melanocyte origin with monoclonal antibodies to melanoma-associated antigens and to HLA antigens. J Natl Cancer Inst 73: 13

    Google Scholar 

  28. Pellegrino MA, Ng A-K, Russo C, Ferrone S (1982) Heterogeneous distribution of the determinants defined by monoclonal antibodies on HLA-A and B antigens bearing molecules. Transplantation 34: 18

    Google Scholar 

  29. Poste G, Doll J, Fidler IJ (1981) Interactions among clonal subpopulations affect stability of the metastatic phenotype in polyclonal populations of B16 melanoma cells. Proc Natl Acad Sci USA 78: 6226

    Google Scholar 

  30. Quaranta V, Pellegrino MA, Ferrone S (1981) Serologic and immunochemical characterization of the specificity of four monoclonal antibodies to distinct antigenic determinants expressed on subpopulations of human Ia-like antigens. J Immunol 126: 548

    Google Scholar 

  31. Rothlein R, Dustin ML, Marlin SD, Springer TA (1986) A human intercellular adhesion molecule (ICAM-1) distinct from LFA-1. J Immunol 137: 1270

    Google Scholar 

  32. Russo C, Callegaro L, Lanza E, Ferrone S (1983) Purification of IgG monoclonal antibody by caprylic acid precipitation. J Immunol Methods 65: 269

    Google Scholar 

  33. Russo C, Pellegrino MA, Ferrone S (1983) A double-determinant immunoassay with monoclonal antibodies to the HLA-A,B,C complex. Transplant Proc 15: 66

    Google Scholar 

  34. Russo C, Pellegrino MA, Ferrone S (1983) A double-determinant immunoassay to quantitate human Ia antigens. Transplant Proc 15: 57

    Google Scholar 

  35. Sood AK, Pereira D, Weissmann SM (1981) Isolation and partial nucleotide sequence of a cDNA clone for human histocompatibility antigen HLA-B by use of an oligodeoxyucleotide primer. Proc Natl Acad Sci USA 78: 616

    Google Scholar 

  36. Spits H, Borst J, Giphart M, Coligan J, Terhorst C, De Vries JE (1984) HLA-DC antigens can serve as recognition elements for human cytotoxic T lymphocytes. Eur J Immunol 14: 299

    Google Scholar 

  37. Thomas PS (1980) Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci USA 77: 5201

    Google Scholar 

  38. Tonnelle C, DeMars R, Long EO (1985) DOβ: a new β chain gene in HLA-D with a distinct regulation of expression. EMBO J 4: 2839

    Google Scholar 

  39. Watson AJ, DeMars R, Trowbridge IS, Bach FH (1983) Detection of a novel -uman class II HLA antigen. Nature 304: 358

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work was supported by the National Institutes of Health grants AI21384, CA37959 and CA39559

Rights and permissions

Reprints and permissions

About this article

Cite this article

Maio, M., Gulwani, B., Tombesi, S. et al. Modulation by cytokines of HLA antigens, intercellular adhesion molecule 1 and high molecular weight melanoma associated antigen expression and of immune lysis of clones derived from the melanoma cell line MeM 50-10. Cancer Immunol Immunother 30, 34–42 (1989). https://doi.org/10.1007/BF01665028

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01665028

Keywords

Navigation