Skip to main content
British Journal of Cancer logoLink to British Journal of Cancer
. 1991 Sep;64(3):445–450. doi: 10.1038/bjc.1991.329

Cellular cytotoxicity mediated by isotype-switch variants of a monoclonal antibody to human neuroblastoma.

C H d'Uscio 1, T W Jungi 1, K Blaser 1
PMCID: PMC1977638  PMID: 1911183

Abstract

The biological property of an antibody is determined by its antigen binding characteristics and its isotype-related effector functions. We have established monoclonal antibodies of different isotypes by stepwise selection and cloning of the hybridoma CE7. The original CE7 secretes an IgG1/kappa (CE7 gamma 1) antibody that recognises a 185 kD cell surface glycoprotein expressed on all human sympatho-adrenomedullary cells. Isotype-switch variants were isolated in the following sequence: from the original CE7 gamma 1, CE7 gamma 2b variants were isolated, and from a CE7 gamma 2b variant CE7 gamma 2a variants were isolated. The antibodies of three different isotype variant cell lines possess identical antigen binding characteristics, but display distinct effector functions as demonstrated by antibody dependent cell-mediated cytotoxicity (ADCC). ADCC was performed with the neuroblastoma line IMR-32 as the target cells, and different FcR gamma positive cells were either freshly isolated from human peripheral blood leukocytes or cultured for 6-10 days and tested as potential effector cells. Tumour lysis mediated by monocyte-derived macrophages depended on the presence of CE7 gamma 2a antibodies; antibodies from the CE7 hybridomas of gamma 2b and gamma 1 isotypes were virtually inactive in ADCC assay. Pre-exposure of macrophages to rIFN-gamma enhanced their ADCC activity, a result that is compatible with the notion that the high affinity Fc IgG receptor (FcR gamma I/CD64) is involved in the triggering of ADCC in macrophages. In contrast to macrophages, mononuclear cells, nonadherent cells and monocytes displayed considerable non-specific lytic activity, which was little influenced by the presence of antibody regardless of the isotype added.

Full text

PDF
445

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Andreesen R., Picht J., Löhr G. W. Primary cultures of human blood-born macrophages grown on hydrophobic teflon membranes. J Immunol Methods. 1983 Feb 11;56(3):295–304. doi: 10.1016/s0022-1759(83)80019-2. [DOI] [PubMed] [Google Scholar]
  2. Cheung N. K., Saarinen U. M., Neely J. E., Landmeier B., Donovan D., Coccia P. F. Monoclonal antibodies to a glycolipid antigen on human neuroblastoma cells. Cancer Res. 1985 Jun;45(6):2642–2649. [PubMed] [Google Scholar]
  3. Clemetson K. J., McGregor J. L., McEver R. P., Jacques Y. V., Bainton D. F., Domzig W., Baggiolini M. Absence of platelet membrane glycoproteins IIb/IIIa from monocytes. J Exp Med. 1985 May 1;161(5):972–983. doi: 10.1084/jem.161.5.972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Conkling P., Klassen D. K., Sagone A. L., Jr Comparison of antibody-dependent cytotoxicity mediated by human polymorphonuclear cells, monocytes, and alveolar macrophages. Blood. 1982 Dec;60(6):1290–1297. [PubMed] [Google Scholar]
  5. Evans A. E., Gerson J., Schnaufer L. Spontaneous regression of neuroblastoma. Natl Cancer Inst Monogr. 1976 Nov;44:49–54. [PubMed] [Google Scholar]
  6. Fanger M. W., Shen L., Graziano R. F., Guyre P. M. Cytotoxicity mediated by human Fc receptors for IgG. Immunol Today. 1989 Mar;10(3):92–99. doi: 10.1016/0167-5699(89)90234-X. [DOI] [PubMed] [Google Scholar]
  7. Feit C., Bartal A. H., Tauber G., Dymbort G., Hirshaut Y. An enzyme-linked immunosorbent assay (ELISA) for the detection of monoclonal antibodies recognizing surface antigens expressed on viable cells. J Immunol Methods. 1983 Mar 25;58(3):301–308. doi: 10.1016/0022-1759(83)90358-7. [DOI] [PubMed] [Google Scholar]
  8. Hellström I., Hellström K. E., Yeh M. Y. Lymphocyte-dependent antibodies to antigen 3.1, a cell-surface antigen expressed by a subgroup of human melanomas. Int J Cancer. 1981 Mar 15;27(3):281–285. doi: 10.1002/ijc.2910270305. [DOI] [PubMed] [Google Scholar]
  9. Hogg N. The structure and function of Fc receptors. Immunol Today. 1988 Jul-Aug;9(7-8):185–187. doi: 10.1016/0167-5699(88)91206-6. [DOI] [PubMed] [Google Scholar]
  10. Hughes M., Marsden H. B., Palmer M. K. Histologic patterns of neuroblastoma related to prognosis and clinical staging. Cancer. 1974 Nov;34(5):1706–1711. doi: 10.1002/1097-0142(197411)34:5<1706::aid-cncr2820340519>3.0.co;2-j. [DOI] [PubMed] [Google Scholar]
  11. Imai K., Pellegrino M. A., Wilson B. S., Ferrone S. Higher cytolytic efficiency of an IgG2 alpha than of an IgG1 monoclonal antibody reacting with the same (or spatially close) determinant on a human high-molecular-weight melanoma-associated antigen. Cell Immunol. 1982 Sep 15;72(2):239–247. doi: 10.1016/0008-8749(82)90472-5. [DOI] [PubMed] [Google Scholar]
  12. Julius M. H., Simpson E., Herzenberg L. A. A rapid method for the isolation of functional thymus-derived murine lymphocytes. Eur J Immunol. 1973 Oct;3(10):645–649. doi: 10.1002/eji.1830031011. [DOI] [PubMed] [Google Scholar]
  13. Jungi T. W., Hafner S. Quantitative assessment of Fc receptor expression and function during in vitro differentiation of human monocytes to macrophages. Immunology. 1986 May;58(1):131–137. [PMC free article] [PubMed] [Google Scholar]
  14. Jungi T. W., Peterhans E. Change in the chemiluminescence reactivity pattern during in vitro differentiation of human monocytes to macrophages. Blut. 1988 May;56(5):213–220. doi: 10.1007/BF00320108. [DOI] [PubMed] [Google Scholar]
  15. Jungi T. W., Rüegg S. J., Morell A. Interferon gamma-treated human macrophages display enhanced cytolysis and generation of reactive oxygen metabolites but reduced ingestion upon Fc receptor triggering. Hum Immunol. 1989 Feb;24(2):77–93. doi: 10.1016/0198-8859(89)90049-9. [DOI] [PubMed] [Google Scholar]
  16. Katz P., Simone C. B., Henkart P. A., Fauci A. S. Mechanisms of antibody-dependent cellular cytotoxicity: the use of effector cells from chronic granulomatous disease patients as investigative probes. J Clin Invest. 1980 Jan;65(1):55–63. doi: 10.1172/JCI109660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kemshead J. T., Black J. Developments in the biology of neuroblastoma: implications for diagnosis and treatment. Dev Med Child Neurol. 1980 Dec;22(6):816–829. doi: 10.1111/j.1469-8749.1980.tb03752.x. [DOI] [PubMed] [Google Scholar]
  18. Kemshead J. T., Goldman A., Fritschy J., Malpas J. S., Pritchard J. Use of panels of monoclonal antibodies in the differential diagnosis of neuroblastoma and lymphoblastic disorders. Lancet. 1983 Jan 1;1(8314-5):12–15. doi: 10.1016/s0140-6736(83)91559-3. [DOI] [PubMed] [Google Scholar]
  19. Kipps T. J., Parham P., Punt J., Herzenberg L. A. Importance of immunoglobulin isotype in human antibody-dependent, cell-mediated cytotoxicity directed by murine monoclonal antibodies. J Exp Med. 1985 Jan 1;161(1):1–17. doi: 10.1084/jem.161.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Momoi M., Kennett R. H., Glick M. C. A membrane glycoprotein from human neuroblastoma cells isolated with the use of a monoclonal antibody. J Biol Chem. 1980 Dec 25;255(24):11914–11921. [PubMed] [Google Scholar]
  21. Müller C. E., Rajewsky K. Isolation of immunoglobulin class switch variants from hybridoma lines secreting anti-idiotope antibodies by sequential sublining. J Immunol. 1983 Aug;131(2):877–881. [PubMed] [Google Scholar]
  22. Pearson G. R. In vitro and in vivo investigations on antibody-dependent cellular cytotoxicity. Curr Top Microbiol Immunol. 1978;80:65–96. doi: 10.1007/978-3-642-66956-9_3. [DOI] [PubMed] [Google Scholar]
  23. Ralph P., Nakoinz I., Diamond B., Yelton D. All classes of murine IgG antibody mediate macrophage phagocytosis and lysis of erythrocytes. J Immunol. 1980 Nov;125(5):1885–1888. [PubMed] [Google Scholar]
  24. Reynolds C. P., Maples J. Modulation of cell surface antigens accompanies morphological differentiation of human neuroblastoma cell lines. Prog Clin Biol Res. 1985;175:13–37. [PubMed] [Google Scholar]
  25. Schönmann S. M., Iyer J., Laeng H., Gerber H. A., Käser H., Blaser K. Production and characterization of monoclonal antibodies against human neuroblastoma. Int J Cancer. 1986 Feb 15;37(2):255–262. doi: 10.1002/ijc.2910370214. [DOI] [PubMed] [Google Scholar]
  26. Steplewski Z., Lubeck M. D., Koprowski H. Human macrophages armed with murine immunoglobulin G2a antibodies to tumors destroy human cancer cells. Science. 1983 Aug 26;221(4613):865–867. doi: 10.1126/science.6879183. [DOI] [PubMed] [Google Scholar]
  27. Ziegler-Heitbrock H. W., Möller A., Linke R. P., Haas J. G., Rieber E. P., Riethmüller G. Tumor necrosis factor as effector molecule in monocyte mediated cytotoxicity. Cancer Res. 1986 Nov;46(11):5947–5952. [PubMed] [Google Scholar]
  28. de Landazuri M. O., Silva A., Alvarez J., Herberman R. B. Evidence that natural cytotoxicity and antibody-dependent cellular cytotoxicity are mediated in humans by the same effector cell populations. J Immunol. 1979 Jul;123(1):252–258. [PubMed] [Google Scholar]

Articles from British Journal of Cancer are provided here courtesy of Cancer Research UK

RESOURCES