Selection of tumor antigens as targets for immune attack using immunohistochemistry: I. Focus on gangliosides
- PMID: 9334808
- DOI: 10.1002/(sici)1097-0215(19970926)73:1<42::aid-ijc8>3.0.co;2-1
Selection of tumor antigens as targets for immune attack using immunohistochemistry: I. Focus on gangliosides
Abstract
Understanding the distribution of tumor-associated antigens on cancers and normal tissues is essential for selection of targets for cancer immunotherapy. Seven carbohydrate antigens, potential targets for immunotherapy, were studied using a panel of well-characterized MAbs by immunohistochemistry on cryostat-cut tissue sections of 13 types of cancers and 18 normal tissues. GD2 and GD3 were present on most cancers of neuroectodermal origin and GD2 was also present on B cell lymphomas. 9-O-acetyl-GD3 was detected only on melanoma while fucosyl GM1 was detected only on small cell lung cancers (SCLC). Surprisingly, GM2 was strongly expressed on all tested tumors, including cancers of neuroectodermal origin and cancers of epithelial origin. Polysialic acid was primarily expressed on SCLC and neuroblastomas. Globo H was present on most cancers of epithelial origin. These antigens were also identified in normal tissues. Fucosyl GM1 was not expressed significantly on any of the normal tissues analyzed. GD3, GD2, GM2 and polysialic acid were detected in normal brain to varying degrees. GM2 and Globo H were expressed on the luminal surface of epithelia of a variety of organs. The unexpected expression of GM2 on a broad range of cancers and normal epithelial tissues was confirmed by loss after methanol fixation and by immune thin layer chromatography.
Similar articles
-
Selection of GM2, fucosyl GM1, globo H and polysialic acid as targets on small cell lung cancers for antibody mediated immunotherapy.Cancer Immunol Immunother. 2005 Oct;54(10):1018-25. doi: 10.1007/s00262-005-0663-8. Epub 2005 May 31. Cancer Immunol Immunother. 2005. PMID: 15926079 Free PMC article.
-
A murine monoclonal antibody detecting N-acetyl- and N-glycolyl-GM2: characterization of cell surface reactivity.Cancer Res. 1986 Aug;46(8):4116-20. Cancer Res. 1986. PMID: 3731079
-
Recombinant antibodies against ganglioside expressed on tumor cells.Cancer Chemother Pharmacol. 2000;46 Suppl:S13-7. doi: 10.1007/pl00014042. Cancer Chemother Pharmacol. 2000. PMID: 10950141
-
Ganglioside antigens in tissue sections of skin, naevi, and melanoma--implications for treatment of melanoma.Cancer Treat Res. 1991;54:137-51. doi: 10.1007/978-1-4615-3938-4_8. Cancer Treat Res. 1991. PMID: 1673856 Review.
-
Ganglioside antigens expressed by human cancer cells.Semin Cancer Biol. 1991 Dec;2(6):401-9. Semin Cancer Biol. 1991. PMID: 1810468 Review.
Cited by
-
Low-Dose Radiation Potentiates the Propagation of Anti-Tumor Immunity against Melanoma Tumor in the Brain after In Situ Vaccination at a Tumor outside the Brain.Radiat Res. 2021 Jun 1;195(6):522-540. doi: 10.1667/RADE-20-00237.1. Radiat Res. 2021. PMID: 33826741 Free PMC article.
-
Immunoreactivity of the 14F7 Mab (Raised against N-Glycolyl GM3 Ganglioside) as a Positive Prognostic Factor in Non-Small-Cell Lung Cancer.Patholog Res Int. 2012;2012:235418. doi: 10.1155/2012/235418. Epub 2012 Feb 26. Patholog Res Int. 2012. PMID: 22482082 Free PMC article.
-
Phase I trial of combined treatment with ch14.18 and R24 monoclonal antibodies and interleukin-2 for patients with melanoma or sarcoma.Cancer Immunol Immunother. 2006 Jul;55(7):761-74. doi: 10.1007/s00262-005-0069-7. Epub 2005 Sep 27. Cancer Immunol Immunother. 2006. PMID: 16187086 Free PMC article. Clinical Trial.
-
Immunization of metastatic breast cancer patients with a fully synthetic globo H conjugate: a phase I trial.Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3270-5. doi: 10.1073/pnas.051626298. Proc Natl Acad Sci U S A. 2001. PMID: 11248068 Free PMC article. Clinical Trial.
-
A vision for vaccines built from fully synthetic tumor-associated antigens: from the laboratory to the clinic.J Am Chem Soc. 2013 Oct 2;135(39):14462-72. doi: 10.1021/ja405932r. Epub 2013 Sep 18. J Am Chem Soc. 2013. PMID: 23944352 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources